CELL MEMBRANE.
Phospholipids of membrane
contains platelet factor -3 ,
imp for blood clotting
process.
Glycoproteins – forming
surface coat of platelets
Prevent sticking of platelets to
endothelium.
Accelerate adherence to
collagen & damaged
endothelium.
Thursday, June 16, 2016
CELL MEMBRANE.
Canalicular system –
surface of platelets
invaginate to form
Canalicular system or
surface connecting system.
Receptors -- For combining
with collagen & fibrinogen.
Precursors of substances
like – Thromboxane A2, PG,
LT & platelet factor 3,4 are
also present.
Thursday, June 16, 2016
MICROTUBULES.
Made up of
Polymerised proteins
called Tubulins.
Forms compact
bundle below
membrane & encircle
whole cytoplasm.
Responsible for
discoid shape.
Thursday, June 16, 2016
GOLGI APPARATUS,
ENDOPLASMIC RETICULUM
Synthesizes various
Enzymes.
Endoplasmic
Reticulum – stores
large amount of
calcium.
Thursday, June 16, 2016
MITOCHONDRIA
Power house of cell.
Produce ATP & ADP.
Thursday, June 16, 2016
CONTRACTILE PROTEINS.
Actin & Myosin – same as those of contractile
proteins of muscle.
Responsible for platelet contraction & clot retraction.
Thrombosthenin
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OTHER PROTEINS
Fibrin stabilizing Factor – Imp in blood coagulation.
Platelet derived growth factor – for growth of vascular
endothelial cells, vascular smooth cells & fibroblast
Involved in repair of damaged blood vessel.
Von-Willebrand factor – for platelet adherence
Thursday, June 16, 2016
GRANULES
Dense granules –
contains phospholipids,
triglycerides, cholesterol,
ATP,ADP, Serotonin (5HT-
which hey obtain while
passing through GIT)
Alpha granules –
contains secreted proteins
as clotting factors, & PDGF
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ENZYMES
Adenosine triphosphatase & enzyme for synthesis
of prostaglandins.
Prostaglandins – acts as a local hormone & have
local vascular & tissue reaction.
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PROPERTIES
Adhesiveness –
whenever comes in
contact with any wet or
rough surface gets
activated & stick to
surface.
Factors responsible are –
collagen, thrombin, ADP,
thromboxane A2, Ca ion
& Von-Willebrand Factor
Thursday, June 16, 2016
PROPERTIES
Aggregation – property
to stick to each other
Factors responsible are
ADP & Thromboxane A2
Agglutination –
property of clumping
together of platelet
Its due to platelet
Agglutinins.
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FUNCTIONS
Role in haemostasis.
Role in clot formation.
Role in clot retraction.
Role in repair of injured blood vessels.
Role in Defense mechanism.
Transport & storage function.
Thursday, June 16, 2016
ROLE IN HAEMOSTASIS.
Haemostasis – spontaneous arrest of bleeding from injured
blood vessel.
Vasoconstriction – by 5HT & other vasoconstrictors
Temporary haemostatic plug – by platelets due to its
property of adhesiveness & aggregation.
Definite haemostatic plug – also initiated by platelets.
Thursday, June 16, 2016
ROLE IN CLOT FORMATION.
Play imp role in formation of intrinsic prothrombin
activator
It is responsible for onset of blood clotting.
Thursday, June 16, 2016
ROLE IN CLOT RETRACTION.
Contraction of
contractile proteins i. e
Actin, Myosin &
Thrombosthenin.
Responsible for clot
Retraction & wound
healing.
Thursday, June 16, 2016
ROLE IN REPAIR OF INJURED
BLOOD VESSELS.
Platelet derived growth
factor (PDGF) in
cytoplasm of platelet
imp for Repair of
Endothelium.
Thursday, June 16, 2016
ROLE IN DEFENCE MECHANISM.
Due to the property of
agglutination , platelets
are capable of
Phagocytosis.
Mainly in Phagocytosis
of carbon particles,
viruses & immune
complexes.
Thursday, June 16, 2016
TRANSPORT & STORAGE
FUNCTION.
Platelet when passes
through GIT takes 5-
HT against
concentration gradient,
stored & transported to
the site of injury.
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NORMAL COUNT &
VARIATIONS.
Normal count.
150,000 – 400,000
per mm3
Avg 2.5 L/mm3
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PHYSIOLOGICAL VARIATIONS.
Age – Less in infant, reach adult level by 3 months of age.
Sex – No difference but during mensturation reduced in
females.
Meal – Increases after meal
Muscular exercise – Increases.
High Altitude – Increases.
Thursday, June 16, 2016
PATHOLOGICAL VARIATIONS.
Thrombocytosis.
Increase in count more than 450,000/mm3
After Splenectomy
After hemorrhage, severe injury, major operation &
parturition.
Myloproliferative Disorders – CML, Polycythemia vera,
Myelofibrosis.
Thursday, June 16, 2016
PATHOLOGICAL VARIATIONS.
Thrombocytopenia
Decrease in count less than
150,000/mm3
ITP
Bone marrow depression
Acute leukemia
Infections
Toxaemia, septicemia &
uremia.
Thursday, June 16, 2016
FORMATION OF PLATELETS.
Stages in platelets
production.(10 days)
Megakaryoblast.
Promegakaryocyte.
Megakaryocyte.
Sites – Bone Marrow
Stem cells – PHSC
CFU- Meg
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MEGAKARYOBLAST.
Earliest recognizable
cells.
CFU-Meg differentiate to
form Megakaryoblast.
Diameter – 20-30 mm
Cytoplasm – small, blue,
Non-granular
Nucleus – large,
oval/kidney shaped
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PROMEGAKARYOCYTE
Megakaryoblast –
Endoreduplication of
nuclear chromatin.
Nuclear chromatin
replicates in multiple of 2
without division of cell.
Large cell with 32 times
diploid content of nuclear
DNA formed.
Cytoplasm – Granular.
Thursday, June 16, 2016
MEGAKARYOCYTE.
Diameter – large cell with
30-90mm in diameter.
Nucleus- single multiloaded.
Cytoplasm – abundant with
red purple granules.
Cell margin – irregular with
many Pseudopodia which
gets detached into blood &
forms platelets.
One Megakaryocyte – 4000
platelets
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CONTROL OF TROMBOPOIESIS.
Thrombopoietin –
Megakaryocyte –
colony stimulating
activity (Meg-CSA)
Thursday, June 16, 2016
LIFE SPAN & FATE OF
PLATELETS.
Life span – 8-12 days
Avg – 10 days.
Fate – Destroyed by tissue macrophage system in
spleen.
Splenomegaly – reduces platelet count.
Splenectomy – increases platelet count.
Thursday, June 16, 2016