Platelets Flashcards

1
Q

What are platelets?

A
  • second most numerous cell in the body
  • produced from megakayrocytes
  • anucleate and highly granular
  • when activated, take on a filapodial form
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2
Q

What are some processes where platelets are involved?

A
  • haemostasis (stopping bleeding)
  • thrombosis
  • metastasis
  • sepsis
  • inflammation
  • many roles rely on granule content
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3
Q

Describe platelet granules

A

two types
- alpha granules: larger and more abundant. contain (anti)coagulants, membrane proteins, growth factors, ce=hemokines and immune and adhesion factors
- dense granules: contain cations, nucleotides, ATP, bioactive amines

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4
Q

How do platelets stop bleeding?

A

constantly surveilling the endothelium. sense damage by surface receptors and activate their granule contents. recruit other platelets and trigger a coagulation cascade resulting in the formation of a haematopoetic plug that stops the bleeding

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5
Q

What are megakaryocytes?

A
  • platelet precursors made in the bone marrow
  • common myeloid progenitors
  • multinucleated and large
  • endomitosis - gets prepared to divide but never does so DNA increases and cell size increases
  • thrombopoietin cytokine drives differentiation
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6
Q

How do megakaryocytes become platelets?

A
  • not fully understood
  • mature MKs migrate to perivascular environment
  • inhibit the ECM, remodel the cytoplasm + membrane to squeeze into blood vessels
  • elongated proplatelets, large proteins and whole MKs enter the vessels
  • broken down into platelets at the lung vasculature due to interactions with endothelial cells and blood flow stress
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7
Q

What are some typical uses of platelets in the clinic?

A
  • prevent bleeding in thrombocytopenia
  • in response to cancer treatment leading to bone marrow malignancy
  • in surgery or in response to haemorrage
  • congenital (Glanzmanns) and aquired (NSAID) platelet defects
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8
Q

What are the two major clinical sources of platelets currently?

A
  • spun from whole blood donations with leukocytes removed by filtration
  • collected from a donor by apheresis - platelets are separated and the rest of the blood is returned to the circulation of the donor
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9
Q

Why is there a need to make platelets in vitro?

A
  • increased demand with an aging population
  • reduced supply and a short shelf life
  • infection risk from donors
  • immune mismatches
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10
Q

What are the two main challenges with making platelets in vitro?

A
  • mechanisms underlying megakarypoesis not fully understood
  • would need 75-150 million mature MKs to make the equivalent of one pack of donated platelets
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11
Q

What is the general process of creating platelets in vitro?

A
  • take human stem cells and differentiate
  • or human adipocytes/fibroblasts + transdifferentiate in 2D culture
  • add to bioreactor to induced platelet formation
  • blood type matching and use
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12
Q

What are the positives and negatives of using haematopoetic stem cells to make platlets in vitro?

A
  • bone marrow + peripheral blood HSCs differentiate well into MKs
  • rare in the circulation
  • multipotent
  • can’t renew forever in culture
  • asynchronous cultures
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13
Q

What are the positives and negatives of using iPSCs to make platelets in vitro?

A
  • self renewing
  • can genetically define and modify
  • proliferation and differentiation can be controlled to synchronize maturation
  • make lower platelet / MK yields
  • mature less well
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14
Q

What is asynchronous culture of stem cells?

A
  • can’t control when each cell matures
  • many cells at different stages
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15
Q

How can iPSCs be used to create immortalised platelet progenitors?

A
  • introduce c-myc, BMI-4, BCL-XL to iPSC-derivedMK precursors or HSCs
  • induce constant proliferation
  • The addition of doxycyclin to MKs causes a huge expansion of MKs
  • when dox is turned off, platelet production begins and all cells one in sync
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16
Q

What 3 factor are important to consider when designing bioreactors for platelet production?

A
  • wall shear stress as blood moves along the endothelium
  • difference in flow from the middle to the outer edges of vessels
  • Reynolds number - predicts flow conditions more smooth or turbulent?
17
Q

What are some current bioreactor examples for platelet production?

A
  • bioreactors with many narrowing chambers
  • flow pushes MKs through
  • mimics lung vasculature
  • forces palatlets to form
18
Q

What are some potential furutre uses of stem cell derived platelets?

A
  • could genetically modify to activate at specific sites
  • could load granules with helpful contents to treat disease or drive expression of desired proteins