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 Also known as:
2
 RES is an essential component of
the immune system.
 The main organs include the liver,
spleen, lymph nodes, bone marrow,
thymus and intestinal tract
associated lymphoid tissue.
3
Cellular components of RES
1. Monocytes.
2. Macrophage Located in all
tissues such as skin (Langerhans
cells ), liver (kupffer), spleen,
bone marrow, lymph nodes, lung.
3. Endothelial cells: bone marrow,
spleen, lymph node.
4
Macrophages
 Often remain fixed to their
organs. They filter and destroy
objects which are foreign to the
body, such as bacteria, viruses.
 Some macrophages are mobile, and
they can group together to
become one big phagocytic cell in
order to ingest larger foreign
particles.
5
Formation of
Macrophages
1. Begin by Stem cell in Bone Marrow:
- Monoblast promonocyte mature monocytes
(released into blood).
2. Stay for 10-20 hours in circulation.
3. Then leave blood to tissues transforming
into larger cells macrophage.
4. Macrophage life span is longer up to few
months in tissues.
6
FIXED TISSUE MACROPHAGES
 Known by different names in different sites.
The nameThe organ
Kupffer cellsLiver
Alveolar macrophagesLung
Langerhans cellsSkin
HistiocytesConnective tissue
MicrogliaCNS
OsteoclastsBone
Reticular or Dendritic
cells
Spleen/Bone
marrow/Lymph nodes
7
Characterized by an increase in:
 Cell size.
 Number and complexity of
intracellular organelles Golgi,
mitochondria, lysosomes.
 Intracellular digestive enzymes.
8
FUNCTIONS OF THE RES
1. Phagocytosis: Bacterial, dead
cells, foreign particles (direct).
2. Immune function: processing
antigen and antibodies production
(indirect).
3. Formation of bile pigments.
4. Breakdown of aging RBC.
5. Storage and circulation of iron.
9
Phagocytosis
 Phagocytosis is part of the
natural or innate immune process.
 Macrophages are a powerful
phagocytic cells:
 Ingest up to 100 bacteria.
 Ingest larger particles such as old
RBC.
 Get rid of waste products.
10
Direct anti-inflammatory
11
Mechanism of phagocytosis
12
Indirect Immune role Of RES
 Indirect immune function of RES:
◦ Ingest foreign body, process it and
present it to lymphocytes.
13
Antigen processing
 Antigen processing: degradation of
proteins into peptides that can be
presented on MHC I or MHC II
◦ MHC I presents peptides derived from
cytoplasmic antigens
◦ MHC II presents peptides derived from
extracellular or intravesicular antigens
14
Antigens are derived from cytosolic
or vesicular compartments
15
 The lymphatic system is composed of:
1. Primary lymphoid organs: include the
bone marrow and the thymus.They create
special immune system cells called
lymphocytes.
2. Secondary lymphoid organs: These organs
include the lymph nodes, the spleen, the
tonsils and certain tissue in various mucous
membrane layers in the body (e.g. in the
bowel).
16
 Lymph nodes filter lymph before it is
returned to the blood
17
 Leukocyte defense cells within
lymph nodes:
◦ Macrophages – engulf and destroy
foreign substances
◦ Lymphocytes – provide immune response
to antigens
18
 Thymus:
◦ Produces hormones (like thymosin) to
program (“educate”) certain lymphocytes
19
 Tonsils:
◦ Small masses of lymphoid tissue around
the pharynx
◦ Trap and remove bacteria and other
foreign materials
20
 Peyer’s Patches:
◦ Found in the wall of the small intestine
◦ Capture and destroy bacteria in the
intestine
21
 It is a soft purple gray in color located in the
left upper quadrant of the abdomen.
 It is a highly vascular lymphoid organ.
 It is the part of RES and its absence leads to
a predisposition toward certain infections.
22
: provides
the immune function of
the spleen.
 Red pulp: surrounds
white pulp, composed
of Venous sinuses filled
with whole blood and
Splenic cords of
reticular connective
tissue rich in
macrophages.
23
1. Haematopoiesis: fetal life.
2. Spleen is a main site for
destruction of RBCs specially old
and abnormal e.g. spherocytosis.
3. Blood is filtered through the
spleen.
4. Reservoir of thrombocytes and
immature erythrocytes.
5. Recycles of iron.
24
1. Because the organ is directly
connected to blood circulation, it
responds faster than other lymph
nodes to blood-borne antigens.
2. Destruction and processing of
antigens.
3. Reservoir of lymphocytes in white
pulp.
4. Site for Phagocytosis of bacteria
and worn-out blood cells.
25
 Impaired splenic function or
splenectomy lead to:
Reduce the ability to make antibody,
particularly to capsulated organisms.
Reduces clearance of intracellular
organisms (e.g. parasitized red
cells).
Impairs defense against organisms
and toxins in the portal circulation.
26
It is the central factory for production of
all adult hematopoietic cells.
27
 Bone marrow is a highly cellular,
viscous , and highly vascular tissue
present within the hollow cavities of
hard bone and is specially designed
to support the proliferation,
differentiation, and maturation of
hematopoietic cells .
28
 Depending on proportion of adipocytes &
hemopoietic cells.
1. RED: (rich in haemopoietic cells).
2. YELLOW: (composed of fat cells)
29
1. Vascular compartment
2. Hematopoietic compartment
a) Hematopoietic cells
b) Stromal cells
30
 Cells of the BM:
Erythroid series
Myeloid series
Megakaryocytic series
Monocytic series
31
Cellularity
(hematopoietic/fat cell)
SiteAge
100/0All bones, liver &
spleen
Newborns
70/30Most bonesChildren
50/50Axial bonesAdults
30/70Axial bonesOld age
32
Marrow cellularity vary according
to age.
Myeloid : Erythroid ratio (M:E)
 The M:E ratio is the ratio of all
granulocytic plus monocytic cells
(Myeloid) to all erythroblasts
(Erythroid).
 Lymphocytes, monocytes and plasma
cells are not included in the M:E ratio.
 The normal ratio of 3:1 to 4:1 reflects
the relationship between production
and life span of the various cell types.
33
Alteration in M:E ratio
 Normal M:E:
Does not reflect changes, as both series
are equally affected—e.g., in aplastic
anaemia, myelosclerosis, chloramphenicol
toxicity.
 Decreased M:E:
- Haemolytic and megaloblastic anaemias.
 Increased M:E:
- CML, leukaemoid reactions.
34
35

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Reticuloendothelial system

  • 1. 1
  • 3.  RES is an essential component of the immune system.  The main organs include the liver, spleen, lymph nodes, bone marrow, thymus and intestinal tract associated lymphoid tissue. 3
  • 4. Cellular components of RES 1. Monocytes. 2. Macrophage Located in all tissues such as skin (Langerhans cells ), liver (kupffer), spleen, bone marrow, lymph nodes, lung. 3. Endothelial cells: bone marrow, spleen, lymph node. 4
  • 5. Macrophages  Often remain fixed to their organs. They filter and destroy objects which are foreign to the body, such as bacteria, viruses.  Some macrophages are mobile, and they can group together to become one big phagocytic cell in order to ingest larger foreign particles. 5
  • 6. Formation of Macrophages 1. Begin by Stem cell in Bone Marrow: - Monoblast promonocyte mature monocytes (released into blood). 2. Stay for 10-20 hours in circulation. 3. Then leave blood to tissues transforming into larger cells macrophage. 4. Macrophage life span is longer up to few months in tissues. 6
  • 7. FIXED TISSUE MACROPHAGES  Known by different names in different sites. The nameThe organ Kupffer cellsLiver Alveolar macrophagesLung Langerhans cellsSkin HistiocytesConnective tissue MicrogliaCNS OsteoclastsBone Reticular or Dendritic cells Spleen/Bone marrow/Lymph nodes 7
  • 8. Characterized by an increase in:  Cell size.  Number and complexity of intracellular organelles Golgi, mitochondria, lysosomes.  Intracellular digestive enzymes. 8
  • 9. FUNCTIONS OF THE RES 1. Phagocytosis: Bacterial, dead cells, foreign particles (direct). 2. Immune function: processing antigen and antibodies production (indirect). 3. Formation of bile pigments. 4. Breakdown of aging RBC. 5. Storage and circulation of iron. 9
  • 10. Phagocytosis  Phagocytosis is part of the natural or innate immune process.  Macrophages are a powerful phagocytic cells:  Ingest up to 100 bacteria.  Ingest larger particles such as old RBC.  Get rid of waste products. 10
  • 13. Indirect Immune role Of RES  Indirect immune function of RES: ◦ Ingest foreign body, process it and present it to lymphocytes. 13
  • 14. Antigen processing  Antigen processing: degradation of proteins into peptides that can be presented on MHC I or MHC II ◦ MHC I presents peptides derived from cytoplasmic antigens ◦ MHC II presents peptides derived from extracellular or intravesicular antigens 14
  • 15. Antigens are derived from cytosolic or vesicular compartments 15
  • 16.  The lymphatic system is composed of: 1. Primary lymphoid organs: include the bone marrow and the thymus.They create special immune system cells called lymphocytes. 2. Secondary lymphoid organs: These organs include the lymph nodes, the spleen, the tonsils and certain tissue in various mucous membrane layers in the body (e.g. in the bowel). 16
  • 17.  Lymph nodes filter lymph before it is returned to the blood 17
  • 18.  Leukocyte defense cells within lymph nodes: ◦ Macrophages – engulf and destroy foreign substances ◦ Lymphocytes – provide immune response to antigens 18
  • 19.  Thymus: ◦ Produces hormones (like thymosin) to program (“educate”) certain lymphocytes 19
  • 20.  Tonsils: ◦ Small masses of lymphoid tissue around the pharynx ◦ Trap and remove bacteria and other foreign materials 20
  • 21.  Peyer’s Patches: ◦ Found in the wall of the small intestine ◦ Capture and destroy bacteria in the intestine 21
  • 22.  It is a soft purple gray in color located in the left upper quadrant of the abdomen.  It is a highly vascular lymphoid organ.  It is the part of RES and its absence leads to a predisposition toward certain infections. 22
  • 23. : provides the immune function of the spleen.  Red pulp: surrounds white pulp, composed of Venous sinuses filled with whole blood and Splenic cords of reticular connective tissue rich in macrophages. 23
  • 24. 1. Haematopoiesis: fetal life. 2. Spleen is a main site for destruction of RBCs specially old and abnormal e.g. spherocytosis. 3. Blood is filtered through the spleen. 4. Reservoir of thrombocytes and immature erythrocytes. 5. Recycles of iron. 24
  • 25. 1. Because the organ is directly connected to blood circulation, it responds faster than other lymph nodes to blood-borne antigens. 2. Destruction and processing of antigens. 3. Reservoir of lymphocytes in white pulp. 4. Site for Phagocytosis of bacteria and worn-out blood cells. 25
  • 26.  Impaired splenic function or splenectomy lead to: Reduce the ability to make antibody, particularly to capsulated organisms. Reduces clearance of intracellular organisms (e.g. parasitized red cells). Impairs defense against organisms and toxins in the portal circulation. 26
  • 27. It is the central factory for production of all adult hematopoietic cells. 27
  • 28.  Bone marrow is a highly cellular, viscous , and highly vascular tissue present within the hollow cavities of hard bone and is specially designed to support the proliferation, differentiation, and maturation of hematopoietic cells . 28
  • 29.  Depending on proportion of adipocytes & hemopoietic cells. 1. RED: (rich in haemopoietic cells). 2. YELLOW: (composed of fat cells) 29
  • 30. 1. Vascular compartment 2. Hematopoietic compartment a) Hematopoietic cells b) Stromal cells 30
  • 31.  Cells of the BM: Erythroid series Myeloid series Megakaryocytic series Monocytic series 31
  • 32. Cellularity (hematopoietic/fat cell) SiteAge 100/0All bones, liver & spleen Newborns 70/30Most bonesChildren 50/50Axial bonesAdults 30/70Axial bonesOld age 32 Marrow cellularity vary according to age.
  • 33. Myeloid : Erythroid ratio (M:E)  The M:E ratio is the ratio of all granulocytic plus monocytic cells (Myeloid) to all erythroblasts (Erythroid).  Lymphocytes, monocytes and plasma cells are not included in the M:E ratio.  The normal ratio of 3:1 to 4:1 reflects the relationship between production and life span of the various cell types. 33
  • 34. Alteration in M:E ratio  Normal M:E: Does not reflect changes, as both series are equally affected—e.g., in aplastic anaemia, myelosclerosis, chloramphenicol toxicity.  Decreased M:E: - Haemolytic and megaloblastic anaemias.  Increased M:E: - CML, leukaemoid reactions. 34
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