red blood cells
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Transcript red blood cells
Blood
and
hemopoiesis
Lecture, 26.4.2012
Blood
structure and function
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„connective tissue“ (cells and ECM )
blood cells and plasma
erythrocytes (red blood cells)
leukocytes (white blood cells)
platelets
serum – differs from plasma by the
absence of factors (oraganic and
anorganic), which leave plasma during
coagulation (has been involved in clot)
hematocrit - the volume of combined
formed elements in the blood after
centrifugation
erythrocytes – 43%
leukocytes and paltelets (buffy coat) 1%
40-50% male
30-40% female
Blood
structure and function
• total volume 5,5L
• transport : oxygen, CO2, nutrients, waste products,
hormones…
• maintaining of acid/base and osmotic balance, body
temperature
• plasma: water, proteins (albumin, globulins, clotting
proteins, complement, lipoproteins), inorganic salts, ions,
nitrogenous compounds, nutrients, gases
Formed elements
Erythrocytes
red blood cells
biconcave-shaped discs without nuclei
size: 7,5 x 2,6 μm (in the middle only 0,8 μm)
shape provides the cell with larger surface area thus enhancing its
capability for the exchange of gases
number: 3,9 – 5,5 milions in 1μL
it depends on age, gender, race and other factors as diet,altitude ect. Therefore,
every country has to determinate and statistically calculate reference values.
plasmalemma (integral proteins: glycophorins, ion channels, anion
transporters), subplasmalemmal cytoskeleton (spectrin, actin
tetramers).. hemoglobin (33%), enzymes: glycolysis, hexosemonophosphate shunt
they survive 120 days in circulation
oligosacharides on the surface, that acts like antigen – AB0 system
determination
Clinical applications
anemia
polycythemia – physiological adaptation or haemoblastosis – it
increases blood viscosity
anisocytosis – higher variability in size
macrocytes – greater – impairment of maturation (deficiency of vit.
B12)
microcytes – smaller (defeiciency of iron)
sicle cell disease/thallasemia – point mutation in the gene for
hemoglobin – HBS shape – abnormal/crescent shape of RBC (red
blood cell) – anemia, small vessels/venules obstruction
Leukocytes – white blood cells
granulocytes a agranulocytes
neutrophil
eosinophil
basophill
lymphocyte
monocytes
• granulocytes
• neutrophils (polymorphonuclear
leucocytes)
• eosinophils
• basophils
• agranulocytes/
mononuclear – see mononuclear
phagocyte system
• lymphocytes , B, T
• monocytes
Leukocytes function
• number 6500 – 10,000 in 1μL
• do not function in blood stream, but use it for transport to
connective tissue, where perform their function
• diapedesis – active migration from blood stream do CT
Granulocytes
content of two granule types:
specific with specific function for particular
garnulocyrte type
nonspecific/azurophilic (lysosomes)
all granulocytes in periferal blood are terminal postmitotic
stages of the cell development – cells do not divide. They
survive only few days in peripheral blood
nuclei are divided in two or more lobes
Neutrophilic granulocytes
60-70% of lekocytes
size: 12-15 μm (in smear)
nucleus is divides in two or three lobes that are connected by
chromatin bridges;
(small appendage to the nucleus inactive second X chromosome – Barr body in
females´neutrophiles good indentified)
specific granules – small, near the limit of resolution in LM lysosomes
azurophilic granules – 0,5 μm
glycogen – source of energy – anaerobic metabolism
phagocytosis, oxidative burst – (H2O2) and oxygen radicals
Neutrophil
• chemoattraction to sites of
microorganism invasion
• phagocytosis of microorganisms
- phagosome
• release of hydrolytic enzymes
and by reactive oxidative
compounds in phagosome
(superoxide, hydrogen peroxide,
hypochlorous acid (oxidative
stress)
• only once perform a
phagocytosis and die (pus)
Eosinophilic granulocytes
2-4%
size: 12-15 μm
bilobed nucleus
specific granules: crystalline
core (internum) – major
basic protein
matrix (externum) - lighter
allergy, parasitic infections
modulation of inflamation
(inactivation of leukotrienes
and histamine)
Basophilic granulocytes
less that 1%
size 12-15 μm
nucleus is divided in irregular
lobes, but it is not distinct
because it is covered by
granules
specific granules –
metachromatic, content of
heparine and histamine –
liberation of granules –
degranulation - after binding
of certain antigens.
similarity between basophil and
mast cell
Lymphocytes
on the basis of size:
small (6-8μm), medium-sized
and large (up to 18μm).
small lymphocytes prevail in
blood – memory cells
large round nucleus,
chromatin is condensed,
nucleolus
thin rim of cytoplasm,
ribosomes, azurophilic
granules
Lymphocyte function
T and B lymphocytes – specific immunity (T lymphocytes
prevail in peripheral blood: 65% - 75% )
B lymphocytes – humoral – differentiation in plasma cells
– production of antibodies
T lymphocytes – cytotoxic CD8 (induce apoptosis) , helper
CD4 (cooperate with B-lymphocytes and macrophages)
NK (natural killers) medium-sized lymphocytes – 10-15%
in peripheral blood – nonspecific - innate immune
response
Monocytes
size: 12 -20μm
oval, horseshoe or kidney
shaped nucleus,
excentrically placed
basophilic cytoplasm,
azurophilic granules
(lysosomes), RER,
polyribosomes,
mitochondria, Golgi
complex
monocytes differentiate
into macrophages (antigen
presenting cells)
Leukocytes - differential white cell count: the distribution of
the diffrent types of white cells present in circulating blood
6 000 -10 000 in 1μL
granulocytes
neutrophiles 60 -70%, 3500-7500
eosinophiles 2-4%,
150 - 400
basophiles 0-1%
agranulocytes
lymphocytes 20-30%
monocytes 3-8%
50-100
1500-2500
200-800
Platelets - thrombocytes
nonnucleated, disc-like cell fragments of megakaryocytes
size - 2-4 μm
200 000– 400 000 in uL
central zone containing granules – granulomera and peripheral
lighter zone - hyalomera
hyalomera: open canalicular system – invagination of superficial
plasmalemma, marginal bundle of microtubules, actin and myosin –
contractile
granulomera: mitochondria, glycogen, granules (δ - dense bodies –
ATP and serotonin; α – platelet-specific proteins: fibrinogen, PdGF,
FGF, von Willebrandt factor, platelet-specific factor IV; λ lysosomes)
hemophilia – inherited deficiency of factor VIII or IX
Von Willebrand disease – the most frequent bleeding disorder, hereditary disease with
abnormal or defect of von Willebrand factor
Platelets
Hemopoeisis
Chick embryo – blood islands, 2ED
• mesoderm of yolk sac
•(3 week)
• intraembryonic splanchnic
mesoderm (3week – 6week)
• liver
• spleen (hepato-lineal period)
•bone marrow (from8week)
Hemopoeisis
hemopoiesis is a result of simultaneous
proliferation and differentiation
hemopoetic stem cells – types and terms:
pluripotent stem cell – self-renewal – low mitotic activity
multipotent stem cell – lymphoid and myeloid stem cells
unipotent - progenitor cells - colony forming cells - self-renewing
– high mitotic activity
precursor cells (blasts) – not self-renewing (lymphoblast,
erythroblast....)
mature cells – (cytes) (lymphocyte, erythrocyte)
Development of blood cells
regulation
microenvironment – cells of
stroma, extracellular matrix
growth factors:
growth factors –
stimulation of mitotic
activity
colony-stimulating factors
(CSF)
hematopoietins
(erythropoietin – synthesis
in kidney, thrombopoeitin
- synthesis in liver)
Red bone marrow
stroma: hematopoietic cords and sinusoids
stroma – reticular connective tissue (reticular cells and
reticular fibres – (collagen type 1 and 3, fibronectin,
laminin and proteoglycans)
sinusoids – capillaries with discontinuous endothelium
stem cells – they can differentiate also in other cellular
types that blood cells – appropriate stimulation is
necessary
Haemopoiesis
Erythropoiesis
Proerythroblast – large cell with loose chromatin, nucleoli and
basophilic cytoplasm
Basophilic erythroblast – condensed nucleus, basophilic
cytoplasm - polyribosomes
Polychromatophilic erythroblast – polyribosomes decrease,
hemoglobin appears
Orthochromatophilic erythroblast – eosinophilic cytoplasmhemoglobin, maximally condensed nucleus – nucleus
expulsion
Reticulocyte – rest of ribosomes – substantia reticulofilamentosa – 1% in peripheral blood
Erythrocyte
Erythropoiesis
erythropoietin, iron, folic acid, cyancobalamin (vit B12)
3 - 5 division from proerythroblast to erythrocyte
approximately 7 days from proerythroblast to reticulocyte
decrease of the cell volume
condensation of chromatin (pycnotic nucleus) and its
expulsion
synthesis of hemoglobin and successive loss of basophilia
(polyribosomes)
Granulopoiesis
Gardual synthesis of azurophilic and later also specific
granules
Myeloblast – finely dispersed chromatin, no granules
Promyelocyte – basophilic cytoplasm, Golgi complex and
azurophilic granules
neutrophilic, basophilic and eosinophilic myelocytes –
condensation of nucleus, appearance of specific granules
neutrophilic metamyelocyte – band cell –
mature granulocyte
Maturation of lymphocytes
no specific morphologic differences
stem cells - progenitors in bone marrow –– they do not
have antigens specific for B and T lymphocytes
maturation in thymus (precursors T- lymphoblasts –
differentiate in mature lymphocytes) or in bone marrow
(B – lymphoblasts, lymphocytes), they may divide in
periphery in lymphoid organs (spleen, lymph node, tonsil)
Maturation of monocytes
monoblast – identical with myeloblast
promonocyte – large cell – up to 18μm; basophilic
cytoplasm, large slightly indented nucleus, large amount
of RER, large Golgi complex
formation of azurophilic granules – lysosomes
in blood, they circulate approximately 8 hours
they survive in periphery for several months –
macrophages - antigen presenting cells
Origin of platelets
megakaryoblast – 15 - 50 μm, large ovoid nucleus,
numerous nucleoli. Polyploid cell - up to 30 sets of
chromosomes (reflecting its size)
megakaryocyte – giant cell - 35 – 150 μm.
irregular nucleus, numerous mitochondria, welldeveloped RER and extensive Golgi complex. Formation of
granules. Invagination of plasmalemma – demarcation
membranes – they surround areas – processes –
fragmentation – release of platelets into the blood
after dessintegration of cytoplasm into the platelets,
megakaryocyte die by apoptosis