10.17.18 Platelet Production and Function Flashcards
Platelets are normally made in the bone marrow from progenitor cells known as ___
megakaryocytes
DNA replication continues, but neither the nucleus nor the cell undergoes division
endomitosis
What does endomitosis produce?
Polyploid cell
Synthesis of this is static and not regulated; made in liver
How are plasma concentrations regulated?
TPO
Platelet production rates and by the total mass of platelets and MK
What is the job of GPIa-IIa
binds collagen
What is another name for GPIa-IIa
a2B1
What is the job of GPIIb-IIIa
binds fibrinogen
What is another name for GPIIb-IIIa
a2bB3
What is the job of GPIb-IX-V
binds von Willebrand factor
What is the job of GPVI
activates platelets by binding to collagen
Platelets stick to injured vessel wall via GP Ib-IX-V binding to VWF
Adhesion
Resting platelets come in contact with agonists that bind to receptors-signaling occurs-platelets change shape, secrete and activate their GP IIb-IIIa integrins
Activation
Platelets stick to each other via fibrinogen bridges binding to activated GP IIb-IIIa
Aggregation
Platelets release granular contents and potentiate clotting
Secretion
Platelet receptors are GP Ia/IIa and GP VI
Collagen
Platelet receptors are P2Y12 and P2Y1
ADP
Platelet receptor is PAR-1
Thrombin
Platelet receptor is a GPCR
Thromboxane
What keeps platelets from sticking to normal endothelium?
- Nitric Oxide
- Exto-ADPase
- Prostacyclin
How do you diagnose Qualitative Platelet Disorders?
Prolonged bleeding time via PFA-100
PT/PTT/TCT should be normal
What are congenital reasons for Qualitative Platelet Disorders?
- Bernard-Soulier
2. Glanzmann’s Thrombesthenia
What are acquired reasons for Qualitative Platelet Disorder?
- Uremia
- ASA, NSAIDs
- Myeloproliferative disease
This is a defect in Ib/IX on platelet surface so there’s no adhesion
Bernard-Soulier
this is a defect in IIb/IIIa on platelet surface so there’s no aggregation
Glanzmann’s thrombaesthenia
What are the symptoms of platelet hypofunction like?
Same defects of primary hemostasis
- Heavy bleeding
- Mucocutaneous bleeding (oozing and bruising)
- Petechia
- Purpura
- Abnormal platelet aggregation leading to stroke/heart attack