This document describes the structure and formation of bone. It discusses the microscopic and macroscopic structure of both compact and cancellous bone, including the cells involved like osteoblasts and osteoclasts. It explains the two types of ossification - endochondral, where bone forms from cartilage, and intramembranous, where bone forms directly from mesenchymal tissue. Key structures of bone are also summarized such as the Haversian system, periosteum, and differences between long, flat, and irregular bones.
Cartilage is a connective tissue structure that is composed of a collagen and proteoglycan-rich matrix and a single cell type: the chondrocyte. Cartilage is unique among connective tissues in that it lacks blood vessels and nerves and receives its nutrition solely by diffusion
a brief ppt description about cartilage which may be usefull for teaching for first year mbbs, bds and paramedical students, hope it is helpfull to everyone
Cartilage is a connective tissue structure that is composed of a collagen and proteoglycan-rich matrix and a single cell type: the chondrocyte. Cartilage is unique among connective tissues in that it lacks blood vessels and nerves and receives its nutrition solely by diffusion
a brief ppt description about cartilage which may be usefull for teaching for first year mbbs, bds and paramedical students, hope it is helpfull to everyone
Definition
Classification Of Salivary Glands
Anatomy of salivary glands
Development of salivary glands
Structure Of Salivary Glands
Histology of major and minor salivary glands
classification of joints. example of different types of joints. different types of joints on the basis of axis of movements. clinical aspects of joints. different between arthritis.
In my presentation, I have described about the anatomy and physiology of bone and also did a elaboration on the pathways which is responsible for bone cells formation. For more details related to bone you can contact me on my email : sheershopramanik24@gmail.com
Definition
Classification Of Salivary Glands
Anatomy of salivary glands
Development of salivary glands
Structure Of Salivary Glands
Histology of major and minor salivary glands
classification of joints. example of different types of joints. different types of joints on the basis of axis of movements. clinical aspects of joints. different between arthritis.
In my presentation, I have described about the anatomy and physiology of bone and also did a elaboration on the pathways which is responsible for bone cells formation. For more details related to bone you can contact me on my email : sheershopramanik24@gmail.com
BONE – AN INTRODUCTION
A bone is a rigid organ that constitutes part of the vertebrate skeleton.
There are around 270 to 300+ bones in Infants which gets reduced to 206 bones in adults.
Bones are dynamic structures that are undergoing constant change and remodelling in
response to the ever-changing environment.
Bones support and protect the various organs of the body, produce red and white blood cells,
store minerals, provide structure and support for the body, and enable mobility.
It has a honeycomb-like matrix internally, which helps to give the bone rigidity.
The largest bone in the body is the femur or thigh-bone, and the smallest is the stapes in
the middle ear.
Bone tissue also called (osseous tissue) is a type of specialized dense connective tissue.
Histology
Junqueira’s Basic Histology Text and Atlas, 15th Ed
The bone of the skeleton is a mineralized vascular type of connective tissue with a solid matrix. The alveolar process is the bony extension of the mandible and maxilla that provides the necessary support for the teeth and serves as a site of attachment for the periodontal ligament fibers. By its resorption and deposition, it also compensates for tooth movement.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
What is greenhouse gasses and how many gasses are there to affect the Earth.moosaasad1975
What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
2. Bone or osseous tissue is a rigid form of
connective tissue comprising most of
the skeleton of higher vertebrates.
Consists of cells, fibers(collagenous)
and ground substance/matrix
(calcified).
Extracellular components are calcified
making it hard and brittle.
3. Ca3(PO4)2 . Ca(OH)2 makes up the
major portion of salts present in bone.
PO4 resemble the structure of
hydroxyapatite.
4. FUNCTIONS
1. Provides for the internal support of
the body attachment of muscles and
tendons for locomotion.
2. Encloses the blood forming elements
of bone marrow and protects vital
organs of the cranial and thoracic
cavities.
6. MACROSCOPIC STRUCTURE of
BONE
2 Forms of bones based on their structure
1. Cancellous or spongy (substantia
spongiosa)
2. Compact (substantia compacta)
CANCELLOUS BONE- consists of a 3
dimensional lattice of branching bony
spicules or trabeculae enclosing a
system of intercommunicating spaces
that are occupied by bone marrow.
7. CANCELLOUS BONE
No haversian
sysytems
Trabeculae are lined
by a delicate layer of
tissue called
ENDOSTEUM which
contains
osteoprogenitor
cells,
osteoblasts,osteocla
sts.
8. COMPACT BONE- appears as a solid
continuous mass containing spaces
seen only with the aid of microscope.
LONG BONE
a. EPIPHYSES- are the two spongy ends
of the long bones.
b. DIAPHYSES- the thick walled hollow
cylinder.
10. c. MEDULLARY CAVITY- central cavity of
the shaft.
d. EPIPHYSEAL PLATE is the cartilaginous
plate separating the epiphyses from the
diaphyses. It is the usual ossification
center in cartilaginous type of bone
formation. It is the place where growth
takes place.
11. e. METAPHYSES are columns of spongy
bone found at the transition between
the epiphyseal plate and the diaphyses.
f. PERIOSTEUM- a layer of connective
tissue that covers the surface of the
bones.
g. ENDOSTEUM is a thin cellular layer
that lines the bone marrow cavity. Both
the periosteum
and the endosteum are endowed with
osteogenic properties.
13. EPIPHYSIS
center of ossification
in the epiphyseal
cartilage SC
D diaphysis
C compact bone
GP growth plate
14. Pericranium is the periosteum that
covers the skull.
All portions of the bone not covered
with articular cartilage is covered with
periosteum.
The periosteum consists of an outer
layer of dense fibrous connective tissue
which contains larger blood vessels.
15. Middle layer of the periosteum is dense
elastic tissue which is adherent to the
bone.
The third layer of the periosteum
contains osteoblasts, especially in
growing bones.
PERFORATING FIBERS OF SHARPEY are
coarse bundles of collagenous fibers
from the outer layer of the periosteum
that penetrate the outer circumferen-
16. tial lamellae and interstitial system of
the bone.
FLAT BONES
- Substancia compacta forms on both
surface, inner and outer tables.
- Layer of spongy bone varying thickness
between these tables constitute the
diploe.
17. MICROSCOPIC STRUCTURE
OF BONES
Structure of Bone in General
1. Matrix is composed of calcified subs-
tance made up of organic and
inorganic elements deposited in
lamellae or layers.
2. Collagenous fibers are embedded in
an amorphous ground substance
consists of inorganic elements Ca, Mg,
18. Na.
3. Osteocytes are found in cavities called
lacunae.
CANALICULI- are extensions of lacunae
where cytoplasmic processes of cells
lodge.It serves as continous system of
intercommunication for th epasssage of
metabolites and nutritive materials.
21. OSTEOPROGENITOR CELLS
Relatively undifferentiated cells having
the capacity for mitosis and for further
structural and functional specialization.
Pale staining oval or elongated nuclei.
Found in free bony surfaces,
endosteum, periosteum, lining the
haversian canals and at the epiphyseal
plate of growing bones.
22. Active during normal growth of bones
and in adult life.
Activated during healing of fractures or
repair of other forms of injury.
Undergo division, transforming into
osteoblasts or unite giving rise to
osteoclasts.
23. OSTEOBLASTS
Responsible for the formation of bone
matrix and found on the surfaces of
developing bones.
Nucleus located often at the end of the
cell farthest from the bony surface.
Elongated mitochondria are fairly
numerous: the golgi apparatus is well
developed, owing to its large content
26. OSTEOCYTES
Principal cells of fully formed bone residing in
lacunae.
Processes of neighboring osteocytes are in
contact at their ends.
Their apposed membranes form gap junctions
or nexuses at their site of contact.
Play an active role in the release of Ca from
bone to blood, thus, it participate in the
homoeostatic regulation of its concentration
in the body fluids.
27. OSTEOLYSIS- it is a physiological
process where bony matrix immediately
surrounding the osteocytes in modified
and bone salt is resorbed.
28. OSTEOCLASTS
Giant multinucleated cells about 20-100
um. In diameter, that are closely
associated with areas of bone
resorption.
Active agents in bone resorption.
Frequently found in shallow concavities
in the surface of the bone called
LACUNAE OF HOWSHIP.
29. OSTEOCLASTS
Specimen with low
serum Ca level.
H howship’s lacunae
O osteoclasts
Os osteoid (organic
matrix before
mineralization)
30. A. SPONGY OR CANCELLOUS
BONE
Found in diploe of flat bones of the skull
and face; in the middle or inner portion
of all other bones.
Found only as a thin portion inside the
diaphysis of long bone but, constitutes
a greater part of the epiphyses.
31. Simple in structure, consists of
irregular, branching bony spicules or
trabeculae (lamellae) that form a
network.
Spicules are made up of layers
consisting organic and inorganic
elements.
32. Cells are embedded in the trabeculae or
spicules.
Cells are small, ovoid in shape with fine
cytoplasmic projections extensding to
the canaliculi.
Trabeculae are thin usually not
penetrated by blood vessels.
Absence of haversian system.
33. Bone cells are nourished by diffusion from the
surface thru the minute bony canaliculi that
interconnect lacunae and extend to the
surface.
Marrow cavities or intertrabecular spaces are
lined by a cellular membrane called
ENDOSTEUM which is composed of flattened
cells that are potential bone and blood
forming cells.
34. B. COMPACT BONE
Found on the outer surface of all bones.
Shaft of diaphyses of long bone, spongy
bone found with in is very thin.
40. PERIOSTEUM
A dense, fibrous membrane covers all
portions of the compact bone except
those covered by articular cartilages.
Outer layer is dense connective tissue
containing blood vessels.
Inner layer is made up of loose
fibroelastic ct containing flattened cells
which are potential osteoblasts or bone
forming cells.
41. Flattened fibroblasts has osteogenic
properties in case of bone injury where
they form new bone.
Immediately beneath the periosteum at
the external surface of the bone are
several lamellae that extend uninterrup-
tedly around the circumference of the
shaft.Constitute the PERIOSTEAL OR
EXTERNAL OR BASIC
CIRCUMFERENTIAL LAMELLAE.
42. Surrounding the central medullary
cavity are several lamellae constituting
the ENDOSTEAL OR INNER
CIRCUMFERENTIAL LAMELLAE.
Between these external and internal
circumferential lamellae are located the
haversian systems.
46. HAVERSIAN SYSTEM
Is the structural and functional unit of
the bone tissue. It consists of the
following:
1. LACUNAE- are the bone spaces that
are arranged concentrically around the
haversian canal.
2. Each lacuna contain the different bone
cells or osteocytes.
47. 3. The lacunae are arranged in layers
called LAMELLAE.
a. inner circumferential lamellae- are
the layers of lacunae that surround the
haversian canal.
b. outer circumferential lamellae are
the layers of lacunae that are found on
the outskirts of the haversian system.
48. c. Interstitial lamellae are the lacunae
found in between the Haversian
systems.
4. Canaliculi are the minute canals that
connect the lacunae.
5. Haversian canal is the big passage at
the center of the Haversian system.
Each canal contains artery and vein and
nerve fibers.
49. 6. Volkmann’s canal is the canal that
serve as the communication between
the Haversian canals.
50.
51. OSSIFICATION
The term used for bone formation.
There are two types:
A. ENDOCHONDRAL- is a type where
bone develops from cartilages.
B. MEMBRANOUS- is a type where the
bone develops from membranes.
52. In both types the following steps
occur:
1. First, there is proliferation of
mesenchymal cells at the site of
ossification.
2. In the endochondral type these cells
differentiate into cartilage cells.
53. 3. The cartilage cells will become the
young bone cells, called osteoblasts.
4. The osteoblasts mature to form
osteocytes which are the bone cells.
5. The bone cells which are matured will
die and form osteoclasts.
6. The osteoclasts will undergo resorption
54. and calcification will take place
leaving a hard substance.
c. The intramembranous type of
ossification occurs in the bones of the
skull.
1. In the area where bone develops are
occupied first by mesenchymal cells.
55. 2. Clusters of mesenchymal cells
differentiate into osteoblasts. These are
taking place in centers of ossification.
3. After their appearance the osteoblasts
secrete the organic matrix of the bone.
4. Osteogenic cells also develop in this
area and this will serve as the source of
the rest of the osteoblasts.
56. 5. Trabeculae develop. This are spicules
that radiate out from the ossification
centers. This result in the formation of
the cancellous bones.