This document provides an overview of the microscopic anatomy of the gingiva. It describes the different layers of the gingival epithelium including the oral epithelium, sulcular epithelium, and junctional epithelium. It also discusses the cellular components and layers of the connective tissue below the epithelium. Key structures are described like desmosomes, hemidesmosomes, and tonofilaments that provide connections between epithelial cells and attachment to underlying tissues. The functions of the different epithelial layers and their roles in barrier function and wound healing are also summarized.
seminar on gingiva
contents:
Introduction
Definition
Development of gingiva
Macroscopic anatomy
Microscopic anatomy
Blood supply
Lymphatic drainage
Nerve supply
Correlation of clinical and microscopic features
Repair/healing of gingiva
Age changes
Gingival diseases
Clinical considerations
Conclusion
References
A presentation on the topic of microscopic section of gingiva. This topic is mostly looked on by periodontists. A very important chapter in the speciality in dentistry of periodontology and implantology department. Basic understanding of microscopic features and clinical features of gingiva is an important topic for post graduate as well as undergraduate students in the dental field.
This presentation describes the gingival recession, its classifications and theories of pathogenesis and different etiological factors in its progression.
seminar on gingiva
contents:
Introduction
Definition
Development of gingiva
Macroscopic anatomy
Microscopic anatomy
Blood supply
Lymphatic drainage
Nerve supply
Correlation of clinical and microscopic features
Repair/healing of gingiva
Age changes
Gingival diseases
Clinical considerations
Conclusion
References
A presentation on the topic of microscopic section of gingiva. This topic is mostly looked on by periodontists. A very important chapter in the speciality in dentistry of periodontology and implantology department. Basic understanding of microscopic features and clinical features of gingiva is an important topic for post graduate as well as undergraduate students in the dental field.
This presentation describes the gingival recession, its classifications and theories of pathogenesis and different etiological factors in its progression.
Aberrant Frenum !!
No worries... When Frenectomy is here.
Hello Periodontists,
Here's the entire process of Frenectomy in a nutshell and various ways to encounter the same.
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Furcation involvement is a common sequela of severe chronic periodontal disease. Its effective management has a profound influence on the outcome of periodontal therapy.
Aberrant Frenum !!
No worries... When Frenectomy is here.
Hello Periodontists,
Here's the entire process of Frenectomy in a nutshell and various ways to encounter the same.
Lets Shoot ...
Furcation involvement is a common sequela of severe chronic periodontal disease. Its effective management has a profound influence on the outcome of periodontal therapy.
• Introduction
• Definitions
• Macroscopic Features
• Microscopic Features
• Blood supply
• Nerve supply
• Lymphatic drainage
• Role of epithelium in defence mechanism
• Oxygen consumption of gingiva
• Correlation of Macroscopic with microscopic features
• Conclusion
Introduction
A sound knowledge of the anatomy of the periodontium and the surrounding hard and soft structures is essential to determine the scope and possibilities of surgical periodontal procedures and to minimize their risks.
Blood vessels, and nerves located in the vicinity of the periodontal surgical field, are particularly important during various surgical procedures.
Arterial Supply
Common Carotid Artery
Carotid Sinus & Carotid Body
Applied Anatomy of CCA
CAROTID PULSE :
CCA may be compressed against the carotid tubercle of transverse process of C6 vertebra about 4cm above the sternoclavicular joint.
External Carotid Artery
Generally it lies anterior to the Internal Carotid Artery.
It is the chief artery of supply to structures in the front of neck, oral cavity and in the face.
In carotid triangle
Crossed superficially by:
Cervical branch of facial nerve
Hypoglossal nerve
Facial, lingual &superior thyroid vein
Deep to artery lies:
Wall of pharynx
Superior laryngeal nerve
Ascending pharyngeal artery
Above the carotid triangle
ECA lies deep in the substance of parotid gland
Branches
Lingual Artery
Principal artery of tongue.
Arises anteromedially from ECA opposite the tip of greater cornu of hyoid bone.
Divided into three parts by hyoglossus muscle.
Applied anatomy
Sublingual artery injury occurs in premolar & molar region, when sharp instrument or rotating disks slips off a lower molar & injure the floor of mouth.
Sublingual and submental arteries may course anteriorly in close proximity to the lingual plate, and branches of these blood vessels enter accessory foramina along the lingual cortex.
Hofschneider et al (1999)
Inadvertent penetration through the lingual cortical plate into the floor of the mouth while preparing an osteotomy can cause arterial trauma, thereby resulting in development of a sublingual or submandibular hematoma
Flanagan D. et al.2003
Facial Artery
ORIGIN: Arises from the ECA just above the tip of greater cornua of hyoid bone.
COURSE:
Runs upwards in neck as cervical part ;
On face as facial part.
Tortuous course—
In neck allows free movements of pharynx during deglutition,
On face allows free movements of mandible , lips, & cheek during mastication & facial expressions, escapes traction & pressure during movements.
Cervical part :
Cervical part runs upwards on superior constrictor of pharynx deep to the posterior belly of digastric.
It grooves the posterior border of submandibular gland, makes S-bend [2 loops]
1st winding down over submandibular gland &
then up over the base of mandible.
Facial part:
The vessel enters the face by winding around the base of the mandible, and by piercing the deep cervical fascia,at the anteroinferior angle of the masseter muscle, here it can be palpated & is called as anaesthetist’s artery. Using contracted masseter as a landmark, pulse of facia
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New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
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- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
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Knee anatomy and clinical tests 2024.pdfvimalpl1234
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micro teaching on communication m.sc nursing.pdfAnurag Sharma
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June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
1. P R E S E N T E D B Y
D R S M S I V A R A M A N
P G IS T Y E A R
GINGIVA
2. Contents
Introduction
Development
Macro anatomy of Gingiva
-Marginal Gingiva
-Gingival Sulcus
-Attached Gingiva
-Interdental Gingiva
Microanatomy of Gingiva
-Gingival Epithelium
-General Aspects
-Outer / Oral Epithelium
-Sulcular Epithelium
-Junctional Epithelium
-Interface Between Epithelium And
Connective Tissue
-Gingival Connective Tissue
-Cellular Elements
-Gingival Fibers
3. Contents
Blood Supply
Lymphatic Drainage
Gingival Innervations
Correlation of Normal Clinical and Microscopic Features
-Color
-Size
-Contour
-Shape
-Consistency
-Surface Texture
-Position
Effects of Aging on Gingival Epithelium and Connective Tissue
Conclusion
References
4. Definition
According to Carranza:
The gingiva is the part of the oral mucosa that covers the
alveolar process of the jaws and surrounds the necks of the
teeth.
According to A A P 1992 :
• The fibrous investing tissue, covered by keratinized epithelium,
which immediately surrounds a tooth and is contiguous with its
periodontal ligament and with the mucosal tissues of the mouth.
5. Development
8-9 weeks (after ovulation)
Gingival or alveolar ridge
12-14 weeks (after ovulation)
Shallow gingival furrow
Gingival furrow in maxillary jaw Gumpads (later)
15 weeks
Epithelial differentiation
Appearance of keratohyaline granules
Epithelial invagination
Formation of labial and gingival furrow
6. Anatomical division
Free or Marginal Gingiva or unattached gingiva
Attached Gingiva
Interdental Gingiva.
7. Free gingiva/Un-attached gingiva/Marginal gingiva
The marginal or unattached
gingiva is the terminal edge
or border of the gingiva that
surrounds the teeth in collar
like fashion .
50% cases- it is demarcated
from the adjacent attached
gingiva by a shallow linear
depression called the free
gingival groove.-Ainamo J
,Loe H :1966
Width-1mm,
8. Gingival sulcus
A Shallow crevice or space around the tooth bounded by
surface of tooth on one side and the epithelium lining the free
margin of the gingiva on the other.
V –shaped
Depth :
Ideal conditions – zero(Gottleib B, Orban B 1933)
Clinically - 2 – 3 mm.
Histological depth -1.8 (0 to 6 mm) (Orban B, Kohler J: 1924)
Histological depth need not be equal to biological depth
9. Attached Gingiva
• Firm, resilient and tightly bound to
the underlying periosteum of
alveolar
bone by connective tissue fibers.
• Coronally: marginal gingiva
•Apically: palatally-palatal mucosa
facially-alveolar mucosa
• Mucogingival junction
• Stippling
• Significance
• Width of attached gingiva
stippling
10. Width of attached gingiva
Distance b/w the MGJ & projection on
the external surface of the bottom of
gingival sulcus/ periodontal pocket.
Fascial aspect:
Greatest -incisor region :
3.5 to 4.5 mm in maxilla
3.3 to 3.9 mm in mandible
Least -first premolar area
1.9 mm in maxilla
1.8mm in mandible
Lingual aspect:
Wider-molar region
Narrow-Incisor region
Increases:
By the age of 4yrs
supraerupted teeth(Ainamo A, Ainamo J)
11. Significance of attached gingiva
Gives support to the marginal gingiva
To protect the periodontium from injury caused by frictional forces
encountered during mastication
Barrier of passage for inflammation
Provides resistance to tensional forces(stresses)
Attached gingiva acts as a buffer between marginal gingiva and
alveolar mucosa
12. Continued.
Lang & Loe,1972: suggested that 2 mm of keratinized
gingiva(corresponding to 1 mm attached gingiva in this
material) is adequate to maintain gingival health.
Wennstorm, 1987: the lack of minimum amount of
attached Gingiva does not necessarily result in a soft tissue
recession. Proper plaque control prevents soft tissue
recession, even when it is out of adequate width.
Mehta P et al,2010: width of attached gingiva is not
significant to maintain periodontal health in the presence of
adequate oral hygiene.
13. Measuring-Attached gingiva
HALL WB, 1982:
The width of attached gingiva is determined by subtracting the
sulcus or pocket depth from total width of gingiva
Total width of gingiva: From MGJ to crest of marginal gingiva
Methods to determine width of attached gingiva:
1.Anatomically.
2.Functionally
a)Tension test
b)Roll test
3.Histochemical staining.
4.Ultrasonic devices
14. Interdental Gingiva
Occupies the gingival embrasure, which is the interproximal space
beneath the area of tooth contact.
Shape: pyramidal or Col shape.
PYRAMIDAL SHAPE:
In this the papilla is located immediately beneath the contact point. It is
present in anterior teeth
15. Col shaped -IG
COL SHAPE
It is valley like depression
that connects the facial
and lingual papilla and
conforms to the shape of
interproximal contact and
present in posterior teeth
Its epithelium is non-
keratinized and same as
Junctional epithelium
17. Gingival epithelium-General aspects
Continuous lining of stratified squamous epithelium.
Function:
Physical barrier to Infection
Participate actively in responding to infection in signaling
further host reactions in integrating innate and acquired
immune responses.
To protect deep structures.
Allow a selective interchange with the oral environment.
18. Microscopic Features
gingiva is composed of the overlying stratified squamous epithelium and
the underlying central core of connective tissue.
the epithelium is predominantly cellular in nature,
the connective tissue is less cellular and composed primarily of collagen
fibers and ground substance.
19. Microscopic Anatomy
The epithelium covering the free gingiva may be differentiated as
follows:
• Oral epithelium (OE),
• Oral Sulcular epithelium (OSE),
• Junctional epithelium (JE),
20. Histology
The boundary between the
oral epithelium (OE) and
underlying connective tissue
(CT) has a wavy course. The
connective tissue portions
which project into the
epithelium are called
connective tissue papillae (CTP)
and are separated from each
other by epithelial ridges – so-
called Rete pegs (ER)
Oral & Sulcular epithelium-Rete
pegs (present)
Junctional epithelium -Absent
21. Cell layers
The oral epithelium is a
keratinized, stratified,
squamous epithelium
which, on the basis of the
degree to which the
keratin-producing cells are
differentiated, can be
divided into the following
cell layers:
1. Basal layer (stratum
basale or stratum
germinativum)
2. Prickle cell layer
(stratum spinosum)
3. Granular cell layer
(stratum granulosum)
4. Keratinized cell layer
(stratum corneum).
22. Stratum basale
The basal layer in made up of cells that synthesis DNA and undergo
mitosis, thus providing new cells. The basal cells and parabasal spinous
cells are referred to a stratum germinativum.
Basal cells
Basal cells are of 2 types
1.Serrated & heavily packed with tonofilaments
2. Non- serrated slow cycling stem cells.
Specialized cells called hemidesmosomes are found on the basal
surface.
Hemidesmosomes Attach epithelium to connective tissue
The lateral borders of adjacent basal cells are closely apposed and
connected by desmosomes
23. Stratum spinosum
In the spinosum strata the spinous cells are irregular polyhedral
and larger than basal cells.
The cells are joined by inter cellular bridges which are
desmosomes and tonofibrils are bundles of tonofilaments.
Spinous layer is the most active in protein synthesis.
Keratinosomes (Odland bodies):
Modified lysosomes
Contains-Acid phospatase
24. Stratum granulosum
Stratum granulosum contains flatter and wider cells. These cells
are larger than the spinous cells.
The layer is so named because of basophilic keratohyaline
granules that it contains.
The nuclei shows signs of degeneration and pyknosis.
Odland body or membrane forms in the upper spinous and
granular cell layers.
25. Stratum corneum
Is made up of keratinized squamous, which are larger and
flatten than the granular cells.
Closely packed, flattened cells that have lost nuclei and most
other organelles as they become keratinized.
The cells are densely packed with tonofilaments.
Clear, rounded bodies probably representing lipid droplets
appear within the cytoplasm of the cell.
26. Regulation
Both epithelial proliferation and maturation are needed for
continuous cells renewal to maintain structural integrity.
The control over these 2 processes is mediated by substances
produced by maturing epithelial cells – Chalones which act by
negative feedback mechanism
27. Key features of keratinisation
Progressive flattening of the cell.
Increased prevalence of tonofilaments.
Intercellular junctions coupled to the production of
keratohyaline granules.
Disappearance of the nucleus
28. Types of keratinization
Three types of surface keratinization can occur in the gingival
epithelium:
Orthokeratinization
Parakeratinization
Nonkeratinization
29. Ultra structure-Gingival epithelium
Each epithelial type have characteristic pattern of cytokeratins.
Keratin proteins are composed of different polypeptide subunits
characterized by their isoelectric points and molecular weights.
Basal cells begin synthesis of low mol. Wt. keratins. Ex.: K19
(40kD).
High mol. Wt. keratins are expressed when they reach superficial
layers. Ex.: K1 (68kD).
30. Other proteins synthesized during maturation process:
Keratolinin
Involucrin
Filaggrin
Corneocyte:
Most differentiated epithelial cell
Composed bundles of keratin tonofilaments + amorphous
matrix of filaggrin & surrounded by a resistant envelope (
keratolinin and involucrin).
31. Epithelial cell connections
Together with intercellular protein-carbohydrate complexes,
cohesion between cells is provided by numerous structures
called “Desmosomes”.
Desmosomes:
Located between the cytoplasm processes of adjacent cells.
Two hemidesmosomes facing each other.
Large number of desmosomes gives a solid cohesion between
cells.
32. Desmosome
A desmosome comprises the
following structural components:
1. The outer leaflets (OL) of the cell
membrane of two adjoining cells,
2. The thick inner leaflets (IL) of the
cell membranes
3. The attachment plaques (AP),
which represent granular and
fibrillar material in the cytoplasm.
34. TIGHT JUNCTIONS (ZONAE OCCLUDENS)
Rarely observed forms of epithelial
cell connections where the
membranes of the adjoining cells
are believed to be fused
38. TYPES OF GINGIVAL EPITHELIUM
1. Oral or outer epithelium
2. Sulcular epithelium
3. Junctional epithelium
39. Oral epithelium
• Covers the crest and outer surface of
the marginal gingiva and the surface
of the attached gingiva.
• 0.2 to 0.3 mm in thickness.
• Keratinized or parakeratinised, or it
may present combinations of these
conditions.
• The oral epithelium is composed of
four layers.
40. Sulcular epithelium
• Lines the gingival sulcus.
• Thin, nonkeratinized stratified squamous epithelium
• No Rete pegs.
• Extends from the coronal limit
of the Junctional epithelium to
the crest of the gingival
margin.
• Hydropic degeneration of cells.
• Contains K4 and K13, K19.
• Don’t have merkel cells.
41. Sulcular epithelium has the potential to keratinize:
• If it is reflected and exposed to the oral cavity.
• If the bacterial flora of the sulcus is totally eliminated.
Outer epithelium loses its keratinization:
• When it is placed in contact with the tooth. These findings
suggest that the local irritation of the sulcus prevents sulcular
keratinization.
Sulcular epithelium is extremely important because it act as
a semi permeable membrane through which injurious
bacterial products pass into gingival fluid.
Less permeable
than JE.
42. Junctional epithelium
• Collarlike band of stratified squamous
non-keratinizing epithelium.
• 3 to 4 layers thick in early life, but the
number increases with age to 10 or even
20 layers.
• Tapers from its coronal end to apical
termination, located at the
cementoenamel junction in healthy
tissue.
• Length: 0.25 to 1.35 mm.
43. • These cells can be grouped in two strata:
The basal layer:
That faces the
connective tissue (External Basal
Lamina)
The suprabasal layer:
That extends to
the tooth surface.– DAT CELLS (Internal
basal lamina)
zones of Junctional epithelium:
1. Apical – germination
2. Middle – adhesion
3. Coronal- permeable.
44. The attachment of the Junctional epithelium to the tooth is reinforced by the
gingival fibers, which brace the marginal gingiva against the tooth surface.
For this reason, the Junctional epithelium and the gingival fibers are
considered together as a functional unit.
45. Concepts on epithelial attachment
1. Gottlieb: gingiva is organically united to surface of enamel. He
termed it as epithelial attachment. (drawback- did not explain
how exactly it attaches.)
2. Waerhaug : in 1952 presented a concept of epithelial cuff, he
concluded that gingival tissues are closely adapted but not organically united.
3. Stern: in 1962 showed the attachment to tooth is through hemidesmosomes,
supported by schroeder and listgarten.
46. Junctional epithelium-Functions
Functions:
Provides attachment to the tooth.
Forms an epithelial barrier against the plaque bacteria.
Rapid cell division and funneling of cells towards the sulcus:
Hinder bacterial colonization and
Repair of damaged tissue occurs rapidly.
Allow GCF:
From connective tissue into crevice – Gingival fluid exudates, PMNs,etc.
From crevice to connective tissue – Foreign material such as carbon particles,
Produces active antimicrobial substances like defensins, lysosomal enzymes,
calprotectin and cathelicidin.
Epithelial cells activated by microbial substances secrete chemokines, e.g. IL-
1, IL-6, IL8 and TNF that attract and activate professional defense cells such as
lymphocytes and PMNs.
47. Gingival crevicular Fluid
• Represented as either as transudate or an exudate.
• Diagnostic or prognostic biomarker of the biologic state of the
periodontium in health and disease.
• GCF flow increases during inflammation and resembles that of
inflammatory exudates.
• Gingival fluid diffuses through the basement membranes.
48. GCF-Functions
Cleanse material from the sulcus.
Contain plasma proteins that may improve adhesion of
epithelium to the tooth
Possess antimicrobial properties
Expert antibody activity to defend the gingiva.
49. Epithelium-CT interface
Ultrastructurally the interface is
composed of 4 elements:
Basal cell plasma membrane.
Lamina lucida: 25 to 45 nm
wide.
Lamina densa: 40 to 60 nm
thickness.
Reticular layer.
From the lamina densa so called
anchoring fibrils project in a
fan shaped fashion into the
connective tissue.
52. GROUND SUBSTANCE
• Fills space between fibers and cells
• Amorphous
• High water content
Composed of:
Proteoglycans:
Hyaluronic acid ,
Chondroitin sulphate
Glycoproteins:
(PAS positive) ,
Fibronectin &Laminin
53. CELLS
The different types of cell present in the connective tissue are:
Fibroblasts
Mast cells
Fixed Macrophages & Histiocytes
Inflammatory cells (Plasma cells, Lymphocytes, Neutrophils)
Adipose cells
Eosinophils
54. Fibroblasts:
Preponderant cellular element in the gingival connective tissue.
Mesenchymal origin.
Play a major role in the development, maintenance, and repair
of gingival connective tissue.
Synthesize :
collagen
elastic fibers
glycoproteins and glycosaminoglycans.
collagen degradation through phagocytosis and the secretion of
Collagenases.
55. The connective tissue fibers are produced by the
fibroblasts and can be divided into:
• Collagen fibers
• Reticulin fibers
• Elastic fibers.(Elaunin,Oxytalan,Elastin)
criteria Reticulin
fibres
Oxytalan
fibres
Elastic
fibres
Location Loose CT Association
with blood
vessels
Less-gingiva
More-PDL
56. Collagen type I:
forms the bulk of the lamina propria
provides the tensile strength to the gingival tissue.
Type IV collagen:
branches between the collagen type I bundles & continuous with
fibers of the basement membrane and the blood vessel walls.
Densely packed collagen bundles that are anchored into the
acellular extrinsic fiber cementum just below the terminal point
of the Junctional epithelium form the connective tissue
attachment.
57. Gingival Fibres-Functions
The connective tissue of the marginal gingiva is densely
collagenous, and it contains a prominent system of collagen fiberbundles called
the gingival fibers.
These fibers consist of type I collagen.
Functions:
To brace the marginal gingiva firmly against the tooth
To provide the rigidity necessary to withstand the forces of
mastication without being deflected away from the tooth
surface
To unite the free marginal gingiva with the cementum of the
root and the adjacent attached gingiva
58. Gingival fibres-Types
The gingival fibers are
arranged in three groups:
1. Dento gingival
2. Circular
3. Transseptal
According Page et.al:
1.Semicircular fibers:
2.Transgingival fibers
Lindhe:
1.Dentoperiosteal fibers
59. • Orginates from cementum and spreads
laterally in to lamina propria
Dento-gingival
• Orginates from periosteum and spreads into
lamina propria
Alveolo-gingival
• Originates from cementum near CEJ into
periosteum of alveolar crest
Dento-periosteal
• Originates from within the free marginal and
attached gingiva coronal to alveolar crest and
encircles each tooth.
Circular
• Originates from interproximal cementum coronal to
crest and courses mesially and distally in the
interdental area into cementum of adjacent teeth
Transseptal
60. • Originates from the periosteum of the lateral
aspect of alveolar process and spreads into
attached gingiva.
Periosteogingival
• Originates from within interdental gingiva and
follows on orofacial course
Inter-papillary
• Originates within the attached gingiva
interwing along dental arch between and
around teeth
Transgingival
• Originates from cementum on distal surface of tooth
spreading buccally and lingually around adjacent tooth
and inserting on mesial cementum of next tooth
Intercircular
• Originates from attached gingiva immediately subjacent to
basement membrane and courses mesiodistallyInter-gingival
• Originates from cementum of the mesial surface of tooth
and courses distally and inserts on the cementum of distal
surface of same tooth
Semicircular
61. Colour
Generally coral pink.
The Color is a result of:
Vascular supply
Thickness
Degree of keratinization of epithelium,
Presence of pigment containing cells.
Color to be correlated with cutaneous pigmentation
62. Melanin
• Melanin (non hemoglobin derived brown pigment)
• Prominent in blacks, diminished in albinos
• Distribution of Oral Pigmentations in blacks:
Gingiva -60% Hard Palate -61% Mucous membrane -22% Tongue -
15%
• As a diffuse , deep purplish discoloration or as irregularly shaped
brown and light brown patches and may appear as early as 3
hours after birth.
63. Size
Sum total of the bulk of cellular and intercellular
elements and their vascular supply.
Alteration in size is a common feature of gingival
disease
64. Contour
Marginal gingiva envelops the teeth in collar like
fashion and follows a scalloped outline on the facial
and lingual surfaces.
straight line - along teeth with relatively flat surfaces.
accentuated - pronounced mesiodistal convexity (e.g.,
maxillary canines) or teeth in labial version horizontal
and thickened - in lingual version.
65. Shape
The shape of the Interdental gingiva is governed by the contour of the
proximal tooth surfaces and the location and shape of the gingival
embrasures.
Anterior-Interdental papillae-pyramidal
Posterior-flattened -buccolingually
Shape depends on:
Presence/absence of contact
Distance btw contact point and osseous crest
Course of CEJ
Width of the approximate tooth surfaces
Presence/absence of recession.
66. Consistency
Firm and resilient
Collagenous nature of the lamina
propria and its contiguity with the
mucoperiosteum determine the
firmness of the attached gingiva.
The gingival fibers contribute to
the firmness of the gingival
margin.
If the gingiva is suppressed, the
proteoglycans become deformed
and recoil when the pressure is
eliminated. Thus, the
macromolecules are important for
the resilience of the gingiva.
67. Surface texture
Orange peel – stippled
Stippling –produced by alternate round protuberance and depressions in the
gingival surface.
A form of adaptive specialization or reinforcement for function –feature of
healthy gingiva
Stippling is best viewed by drying Gingiva.
Attached Gingiva is stippled,
Central portion of Interdental papilla is usually stippled.
Less prominent or absent-lingual surfaces.
68. Position
The level at which the gingival margin is attached to the tooth.
Continuous eruption, even after meeting their functional antagonists
occurs through out life .
Active Eruption :Movement of teeth in the direction of occlusal plane
Passive Eruption: Exposure of the tooth by apical migration of Gingiva
Gottlieb : active and passive eruption go hand in hand.
Exposure of the tooth via the apical migration of the gingiva is called gingival
recession or atrophy.
70. Repair/Healing of gingiva
Turnover rate is 10-12 days.
It is one of the best healing tissues in the body with
little or no scarring.
However the reparative capacity is lesser than that of
periodontal ligament and epithelial tissue.
71. Age changes
Stippling usually disappears with age.
Width of the attached gingiva increases with age.
a. Gingival epithelium:
Thinning and decreased keratinization
Rete pegs flatten
Migration of Junctional epithelium apically.
Reduced oxygen consumption.
b. Gingival connective tissue:
Increased rate of conversion of soluble to insoluble collagen
Increased mechanical strength of collagen
Increased denaturing temperature of collagen
Decreased rate of synthesis of collagen
Greater collagen content.
72. Biological width
The biological width is
defined as the dimension of
the soft tissue, which is
attached to the portion of
the tooth coronal to the
crest of the alveolar bone.
Gargiulo et al.,:
They reported the following
mean dimensions:
It is the sum of the epithelial
and connective tissue
measurements
73. Continued.
Biologic Width Evaluation:
Clinical (discomfort when the restoration margin levels are being
assessed with a periodontal probe)
Radiographs (for interproximal violation but mesiofacial and distofacial
line angle not seen properly)
Bone sounding (probing under anesthesia) If this distance is less than 2
mm or more at one or more locations, a diagnosis of biologic width
violation can be confirmed
Biologic width violation:
• Unpredictable bone loss
• Gingival recession
• Persistence of gingivitis
74. References
Clinical Periodontology By Carranza, 12th Edition
Clinical Periodontology And Implant Dentistry By Jan Lindhe,
4th Edition.
Biology Of Periodontal Connective Tissue-bartold And Sampath
Narayana
Oral Histology, Development, Structure And Function – A.R.
Tencate, 5th Edition
PERIODONTICS REVISITED Shalu Bathla, 1st Edition
Babita Pawar, Pratishtha Mishra, Parmeet Banga, and P . P .
Marawar.Gingival zenith and its role in redefining esthetics: A
clinical study. J Indian Soc Periodontol. 2011 Apr-Jun; 15(2): 135–
138.
75. Continued.
Niklaus P . Lang, and Harald Löe. The Relationship Between the
Width of Keratinized Gingiva and Gingival Health. J Periodontol.
1972 Oct;43(10):623-7.
Gerald M. Bowers. A Study of the Width of Attached Gingiva.
Journal of Periodontology,May 1963, Vol. 34, No. 3, Pages 201-
209
Wennström JL. Lack of association between width of attached
gingiva and development of soft tissue recession. A 5-year
longitudinal study. J Clin Periodontol. 1987 Mar;14(3):181-4
Mehta P, Lim LP. The width of the attached gingiva--much ado
about nothing? J Dent. 2010 Jul;38(7):517-25.
Molecular and Cell Biology of the Gingiva, Periodontology 2000;
Vol 24; 2000; 28-55.
83. Development
The gingival tissues develop as a site-specific portion of the oral mucous membrane prior to the
eruption of deciduous teeth.
Unlike the 3 other tissues of the periodontium (i.e.) root cementum, alveolar bone proper and
the periodontal ligament, the gingiva does not derive from the mesenchymal dental follicle
proper. It is a derivative of the stomodeal ectoderm and mesoderm.
The gingival or alveolar ridge 1st appears about 8-9 weeks after ovulation as a result of formation
of labial and gingival furrow
About 12-14 weeks after ovulation a shallow gingival furrow is formed via an epithelial
invagination. The development of the gingival furrow, particularly in the maxillary jaw is
associated with the formation of gum pads later in fetal life.
About 15 weeks after ovulation epithelial differentiation commences when there is the 1st
appearance of keratohyaline granules in the superficial cell layers.
The connective tissue component of the gingiva derives from the perifollicular mesencyme and
develops between the tooth germ and epithelium lining the stomodeum at the gingival ridge.
84. Structural and Metabolic characteristic of the gingival
epithelium.
Keratins – K1, K2 and K10, K11 which are specific to epidermal differentiation
are expressed which high intensity in orthokeratinized areas and with less
intensity in parakeratinised areas.
Parakeratinised areas express K-19 which is usually absent from
orthokeratinized normal epithelial.
Editor's Notes
The most apical point of the marginal gingival scallop - gingival zenith. Its apico-coronal and mesiodistal dimensions vary between 0.06 and 0.96 mm.
The facial and lingual surfaces are tapered toward the interproximal contact area, whereas the mesial and distal surfaces are slightly concave.
Reticulin fibres:
• Have argyrophilic property and are numerous in tissue adjacent to basement
membrane.
• Found in large number in loose CT surrounding blood vessel
• Hence found in endothelial-CT and epithelium-CT interface.
Elastic fibres:
• Only present in association with blood vessels.
• Gingiva seen coronal to mucogingival junction has no elastic fibres except in assocation with blood vessels.
• Alveolar mucosa may have many elastic fibres.
Oxytalan fibres.
• Initially described by Fullmer.
• Modified type of elastic fibres.
• Scarce in gingiva but more in PDL.
• Have thin fibrils with 150 A0 dia.
Synthesis of Melanin pigmentation
• Tyrosine is hydroxylated into DOPA in presence of Tyrosinase enzyme.
• DOPA (Dihydroxy Phenylalanine) is converted into Melanin
• Melanin is phagocytosed to become Melanophages or Melanophores
Stippling –produced by alternate round protuberance and depressions in the gingival surface.
A form of adaptive specialization or reinforcement for function –feature of healthy gingiva
Reduction of stippling – common sign of Gingival disease.
Stippling returns when gingiva is restored to health.
Keratinization – protective adaptation , increased by tooth brushing.
In 40% of adults Gingiva show stippling.
Generalized absence of stippling is seen in:
Infancy Diseased conditions like gingival enlargements, mucocutaneous lesions affecting gingiva, inflammation etc.,
Active eruption is coordinated with attrition, to compensate for tooth substance worn away.
According to the concept of continuous eruption, the gingival sulcus may be located on the crown, the cementoenamel junction, or the root, depending on the age of the patient and the stage of eruption. Rate of active eruption is in pace with tooth wear in order to preserve vertical dimension.
Attrition reduces the clinical crown and prevents it from becoming disproportionately long in relation to the clinical root, thus avoiding excessive leverage on periodontal tissue.
Therefore, some root exposure with age would be considered normal and referred to as physiologic recession. Again, this concept is not accepted at present. Excessive exposure is termed pathologic recession
Established that there is a definite proportional relationship between the alveolar crest, the connective tissue attachment, the epithelial attachment, and the sulcus depth.
They reported the following mean dimensions: