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Platelet count

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Platelet count

"Platelets" redirects here. For the journal, see Platelets (journal).
Platelet
Image from a light microscope (40×) from a peripheral blood smear surrounded by red blood cells. One normal platelet can be seen in the upper left side of the image (purple) and is significantly smaller in size than the red blood cells (stained pink). Two giant platelets (stained purple) are also visible.
Latin thrombocytes
Code Template:TerminologiaHistologica


Platelets, or thrombocytes (from Greek θρόμβος, "clot" and κύτος, "cell"), are small, disk shaped clear cell fragments (i.e. cells that do not have a nucleus), 2–3 µm in diameter,[1] which are derived from fragmentation of precursor megakaryocytes.  The average lifespan of a platelet is normally just 5 to 9 days. Platelets are a natural source of growth factors. They circulate in the blood of mammals and are involved in hemostasis, leading to the formation of blood clots.

If the number of platelets is too low, excessive bleeding can occur. However, if the number of platelets is too high, blood clots can form (thrombosis), which may obstruct blood vessels and result in such events as a stroke, myocardial infarction, pulmonary embolism or the blockage of blood vessels to other parts of the body, such as the extremities of the arms or legs.  An abnormality or disease of the platelets is called a thrombocytopathy,[2] which could be either a low number of platelets (thrombocytopenia), a decrease in function of platelets (thrombasthenia), or an increase in the number of platelets (thrombocytosis). There are disorders that reduce the number of platelets, such as heparin-induced thrombocytopenia (HIT) or thrombotic thrombocytopenic purpura (TTP) that typically cause thromboses, or clots, instead of bleeding.

Platelets release a multitude of growth factors including platelet-derived growth factor (PDGF), a potent chemotactic agent, and TGF beta, which stimulates the deposition of extracellular matrix.  Both of these growth factors have been shown to play a significant role in the repair and regeneration of connective tissues.  Other healing-associated growth factors produced by platelets include basic fibroblast growth factor, insulin-like growth factor 1, platelet-derived epidermal growth factor, and vascular endothelial growth factor.  Local application of these factors in increased concentrations through Platelet-rich plasma (PRP) has been used as an adjunct to wound healing for several decades.[3][4][5][6][7][8][9]

Kinetics

  • The physiological range for platelets is (150 – 400) × 103 per mm3.
  • Platelets are produced in blood cell formation (thrombopoiesis) in bone marrow, by budding off from megakaryocytes.
  • Megakaryocyte and platelet production is regulated by thrombopoietin, a hormone usually produced by the liver and kidneys.
  • Each megakaryocyte produces between 5,000 and 10,000 platelets.
  • Around 1011 platelets are produced each day by an average healthy adult.
  • Reserve platelets are stored in the spleen, and are released when needed by sympathetically induced splenic contraction.
  • The lifespan of circulating platelets is 5 to 9 days.
  • Old platelets are destroyed by phagocytosis in the spleen and by Kupffer cells in the liver.

Thrombus formation

The function of platelets is the maintenance of hemostasis.  This is achieved primarily by the formation of thrombi, when damage to the endothelium of blood vessels occurs. Conversely, thrombus formation must be inhibited at times when there is no damage to the endothelium. These processes are regulated through thromboregulation.

Activation

The inner surface of blood vessels is lined with a thin layer of endothelial cells that, in normal hemostasis, acts to inhibit platelet activation by producing nitric oxide, endothelial-ADPase, and PGI2.  Endothelial-ADPase clears away the platelet activator, ADP.

Endothelial cells produce a protein called von Willebrand factor (vWF), a cell adhesion ligand, which helps endothelial cells adhere to collagen in the basement membrane. Under physiological conditions, collagen is not exposed to the bloodstream. vWF is secreted constitutively into the plasma by the endothelial cells, and is stored in granules within the endothelial cell and in platelets.

When the endothelial layer is injured, collagen, vWF and tissue factor from the subendothelium is exposed to the bloodstream. When the platelets contact collagen or vWF, they are activated (e.g. to clump together). They are also activated by thrombin (formed with the help of tissue factor). They can also be activated by a negatively charged surface, such as glass. Non-physiological flow conditions (especially high values of shear stress) caused by arterial stenosis or artificial devices (Mechanical Heart Valves, blood pumps etc.) can also lead to platelet activation.[10]

Platelet activation further results in the scramblase-mediated transport of negatively charged phospholipids to the platelet surface.  These phospholipids provide a catalytic surface (with the charge provided by phosphatidylserine and phosphatidylethanolamine) for the tenase and prothrombinase complexes. Calcium ions are essential for binding of these coagulation factors.

Shape change

Activated platelets change in shape to become more spherical, and pseudopods form on their surface.  Thus they assume a stellate shape.

Granule secretion

Platelets contain alpha and dense granules.  Activated platelets excrete the contents of these granules into their canalicular systems and into surrounding blood.  There are three types of granules:

Thromboxane A2 synthesis

Platelet activation initiates the arachidonic acid pathway to produce TXA2.  TXA2 is involved in activating other platelets and its formation is inhibited by COX inhibitors, such as aspirin.

Adhesion and aggregation

Platelets aggregate, or clump together, using fibrinogen and von Willebrand factor (vWF) as a connecting agent. The most abundant platelet aggregation receptor is glycoprotein IIb/IIIa (gpIIb/IIIa); this is a calcium-dependent receptor for fibrinogen, fibronectin, vitronectin, thrombospondin, and vWF. Other receptors include GPIb-V-IX complex (vWF) and GPVI (collagen).

Activated platelets will adhere, via glycoprotein (GP) Ia, to the collagen that is exposed by endothelial damage. Aggregation and adhesion act together to form the platelet plug. Myosin and actin filaments in platelets are stimulated to contract during aggregation, further reinforcing the plug.

Platelet aggregation is stimulated by ADP, thromboxane, and α2 receptor-activation, but inhibited by other inflammatory products like PGI2 and PGD2. Platelet aggregation is enhanced by exogenous administration of anabolic steroids.

Wound repair

Main article: Wound repair

The blood clot is only a temporary solution to stop bleeding; vessel repair is therefore needed. The aggregated platelets help this process by secreting chemicals that promote the invasion of fibroblasts from surrounding connective tissue into the wounded area to completely heal the wound or form a scar. The obstructing clot is slowly dissolved by the fibrinolytic enzyme, plasmin, and the platelets are cleared by phagocytosis.

ADP (purinergic/P2) receptors

Human platelets have three types of P2 receptors: P2X(1), P2Y(1) and P2Y(12). Although abnormalities in all three genes have been documented, but clinical correlation is available only for P2Y(12).[11] Patients with P2Y(12) defects have a mild to moderate bleeding diathesis, characterized by mucocutaneous bleeding and excessive post-surgical and post-traumatic blood loss. A defects in P2Y(12) should be suspected when ADP, even at concentrations ≥10 micro molar, is unable to induce full, irreversible platelet aggregation. Confirmation of the diagnosis is with tests that evaluate the degree of inhibition of adenylyl cyclase by ADP.

Other functions

Cytokine signaling

In addition to being the chief cellular effector of hemostasis, platelets are rapidly deployed to sites of injury or infection, and potentially modulate inflammatory processes by interacting with leukocytes and by secreting cytokines, chemokines, and other inflammatory mediators.[13][14][15][16] Platelets also secrete platelet-derived growth factor (PDGF).

Role in disease


High and low counts

A normal platelet count in a healthy individual is between 150,000 and 450,000 per μL (microlitre) of blood ((150–450)×109/L).[17]  Ninety-five percent of healthy people will have platelet counts in this range.  Some will have statistically abnormal platelet counts while having no demonstrable abnormality. However, if it is either very low or very high, the likelihood of an abnormality being present is higher.

Both thrombocytopenia and thrombocytosis may present with coagulation problems.  In general, low platelet counts increase bleeding risks; however there are exceptions (such as immune-mediated heparin-induced thrombocytopenia or paroxysmal nocturnal hemoglobinuria). High counts may lead to thrombosis, although this is mainly when the elevated count is due to myeloproliferative disorder.

Transfusion is generally used only to correct unusually low platelet counts (typically below (10–15)×109/L). Transfusion is contraindicated in thrombotic thrombocytopenic purpura (TTP), as it fuels the coagulopathy. In patients undergoing surgery, a level below 50×109/L is associated with abnormal surgical bleeding, and regional anaesthetic procedures such as epidurals are avoided for levels below 80×109/L.[18]

Normal platelet counts are not a guarantee of adequate function.  In some states, the platelets, while being adequate in number, are dysfunctional.  For instance, aspirin irreversibly disrupts platelet function by inhibiting cyclooxygenase-1 (COX1), and hence normal hemostasis.  The resulting platelets are unable to produce new cyclooxygenase because they have no DNA.  Normal platelet function will not return until the use of aspirin has ceased and enough of the affected platelets have been replaced by new ones, which can take over a week.  Ibuprofen, another NSAID, does not have such a long duration effect, with platelet function usually returning within 24 hours,[19] and taking ibuprofen before aspirin sometimes may prevent the irreversible effects of aspirin.[20]  Uremia, a consequence of renal failure, leads to platelet dysfunction that may be ameliorated by the administration of desmopressin.

Medications

Main article: Antiplatelet drug

Oral agents often used to alter/suppress platelet function include aspirin, clopidogrel, cilostazol, ticlopidine, ticagrelor and prasugrel.

Intravenous agents often used to alter/suppress platelet function include: abciximab, eptifibatide, tirofiban.

In addition to platelet transfusion, hematopoetic agents such as Oprelvekin, Romiplostim, and Eltrombopag can be used to increase platelet counts.

Diseases

Disorders leading to a reduced platelet count:

Alloimmune disorders

Disorders leading to platelet dysfunction or reduced count:

Disorders featuring an elevated count:

Disorders of platelet adhesion or aggregation:

Disorders of platelet granule amount or release

Disorders of platelet metabolism

  • Decreased cyclooxygenase activity, induced or congenital
  • Storage pool defects, acquired or congenital

Disorders that compromise platelet signaling:

Disorders in which platelets play a key role:

Laboratory findings in various platelet and coagulation disorders (V - T)
Condition Prothrombin time Partial thromboplastin time Bleeding time Platelet count
Vitamin K deficiency or warfarin Prolonged Normal or mildly prolonged Unaffected Unaffected
Disseminated intravascular coagulation Prolonged Prolonged Prolonged Decreased
Von Willebrand disease Unaffected Prolonged or unaffected Prolonged Unaffected
Hemophilia Unaffected Prolonged Unaffected Unaffected
Aspirin Unaffected Unaffected Prolonged Unaffected
Thrombocytopenia Unaffected Unaffected Prolonged Decreased
Liver failure, early Prolonged Unaffected Unaffected Unaffected
Liver failure, end-stage Prolonged Prolonged Prolonged Decreased
Uremia Unaffected Unaffected Prolonged Unaffected
Congenital afibrinogenemia Prolonged Prolonged Prolonged Unaffected
Factor V deficiency Prolonged Prolonged Unaffected Unaffected
Factor X deficiency as seen in amyloid purpura Prolonged Prolonged Unaffected Unaffected
Glanzmann's thrombasthenia Unaffected Unaffected Prolonged Unaffected
Bernard-Soulier syndrome Unaffected Unaffected Prolonged Decreased or unaffected
Factor XII deficiency Unaffected Prolonged Unaffected Unaffected
C1INH deficiency Unaffected Shortened Unaffected Unaffected

Discovery

Although red blood cells had been known since van Leeuwenhoek (1632–1723), the German anatomist Max Schultze (1825–1874) was the first to describe platelets.[25][26]  He described "spherules" that were much smaller than red blood cells and that occasionally clumped and were found in collections of fibrous material

Giulio Bizzozero (1846–1901), building on Schultze's findings, used "living circulation" to study blood cells of amphibians microscopically in vivo.  He is especially noted for discovering that platelets clump at the site of blood vessel injury, a process that precedes the formation of a blood clot.  This observation confirmed the role of platelets in coagulation.[27]

In transfusion medicine

Platelets are either isolated from collected units of whole blood and pooled to make a therapeutic dose or collected by apheresis, sometimes concurrently with plasma or red blood cells. The industry standard is for platelets to be tested for bacteria before transfusion to avoid septic reactions, which can be fatal. Recently the AABB Industry Standards for Blood Banks and Transfusion Services (5.1.5.1) has allowed for use of pathogen reduction technology as an alternative to bacterial screenings in platelets.[28]

Pooled whole-blood platelets, sometimes called “random” platelets, are made primarily by two methods.[29] In the US, a unit of whole blood is placed into a large centrifuge in what is referred to as a “soft spin.” At these settings, the platelets remain suspended in the plasma. The platelet-rich plasma (PRP) is removed from the RBCs, then centrifuged at a faster setting to harvest the platelets from the plasma. In other regions of the world, the unit of whole blood is centrifuged using settings that cause the platelets to become suspended in the “buffy coat” layer, which includes the platelets and the white blood cells. The “buffy coat” is isolated in a sterile bag, suspended in a small amount of red blood cells and plasma, then centrifuged again to separate the platelets and plasma from the red and white blood cells. Regardless of the initial method of preparation, multiple donations may be combined into one container using a sterile connection device to manufacture a single product with the desired therapeutic dose.

Apheresis platelets are collected using a mechanical device that draws blood from the donor and centrifuges the collected blood to separate out the platelets and other components to be collected. The remaining blood is returned to the donor. The advantage to this method is that a single donation provides at least one therapeutic dose, as opposed to the multiple donations for whole-blood platelets. This means that a recipient is not exposed to as many different donors and has less risk of transfusion-transmitted disease and other complications. Sometimes a person such as a cancer patient who requires routine transfusions of platelets will receive repeated donations from a specific donor to further minimize the risk. Pathogen reduction of platelets using for example, riboflavin and UV light treatments can also be carried out to reduce the infectious load of pathogens contained in donated blood products, thereby reducing the risk of transmission of transfusion transmitted diseases.[30][31]

Platelets do not need to be cross-matched to ensure immune compatibility between donor and recipient unless they contain a significant amount of red blood cells (RBCs). The presence of RBCs results in a reddish-orange color to the product, and is usually associated with whole-blood platelets. Apheresis methods are more efficient than “soft spin” centrifugation at isolating the specific components of blood needed. An effort is usually made to issue type specific platelets, but this is not as critical as it is with RBCs.

Platelets collected by either method have a very short shelf life, typically five days. This results in frequent problems with short supply, as testing the donations often requires up to a full day. Since there are no effective preservative solutions for platelets, they lose potency quickly and are best when fresh.

Platelets are stored under constant agitation at 20–24 °C. Storage at room temperature provides an environment where any bacteria that are introduced to the blood component during the collection process may proliferate and subsequently cause bacteremia in the patient. Regulations are in place in the United States that require products to be tested for the presence of bacterial contamination before transfusion.[32]

Volume reduction of platelets

Platelets, either apheresis-derived or random-donor, can be processed through a volume reduction process. In this process, the platelets are spun in a centrifuge and the excess plasma is removed, leaving 10 to 100 mL of platelet concentrate. Such volume-reduced platelets are normally transfused only to neonatal and pediatric patients, when a large volume of plasma could overload the child's small circulatory system. The lower volume of plasma also reduces the chances of an adverse transfusion reaction to plasma proteins.[33] Volume reduced platelets have a shelf life of only four hours.[34]

Other species

Nucleated thrombocytes of nonmammalian vertebrates differ from the mammalian thrombocytes not only in having a nucleus and resembling B lymphocytes, but also these nucleated thrombocytes do not aggregate in response to ADP, serotonin and adrenaline (although they do aggregate with thrombin).

See also

References

External links

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