Platelet Aggregation (Plug Formation) (Homo sapiens)

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107-9cytosolCatecholamineGPIb-IX-V complexGP1b-IX-V complex:activated thrombin (factor IIa)Alpha-2 adrenoceptorActivated thrombin (factor IIa)Integrin alphaIIb beta3 signalingAlpha-2 adrenoceptor:Catecholamine1-6


Description

The tethering of platelets to the site of vascular injury is the first step in the formation of a platelet thrombus. Firm adhesion of these tethered platelets, as well as the additional recruitment of others onto their surface leads to the formation of large platelet aggregates. The formation of a thrombus is strictly dependent on the formation of interplatelet bonds.

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Bibliography

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  1. Hehlgans S, Haase M, Cordes N.; ''Signalling via integrins: implications for cell survival and anticancer strategies.''; PubMed Europe PMC Scholia
  2. Weinshank RL, Zgombick JM, Macchi M, Adham N, Lichtblau H, Branchek TA, Hartig PR.; ''Cloning, expression, and pharmacological characterization of a human alpha 2B-adrenergic receptor.''; PubMed Europe PMC Scholia
  3. Dumas JJ, Kumar R, Seehra J, Somers WS, Mosyak L.; ''Crystal structure of the GpIbalpha-thrombin complex essential for platelet aggregation.''; PubMed Europe PMC Scholia
  4. Varga-Szabo D, Pleines I, Nieswandt B.; ''Cell adhesion mechanisms in platelets.''; PubMed Europe PMC Scholia
  5. Hirasawa A, Horie K, Tanaka T, Takagaki K, Murai M, Yano J, Tsujimoto G.; ''Cloning, functional expression and tissue distribution of human cDNA for the alpha 1C-adrenergic receptor.''; PubMed Europe PMC Scholia
  6. Calderwood DA.; ''Integrin activation.''; PubMed Europe PMC Scholia
  7. Kasirer-Friede A, Kahn ML, Shattil SJ.; ''Platelet integrins and immunoreceptors.''; PubMed Europe PMC Scholia
  8. Shattil SJ, Newman PJ.; ''Integrins: dynamic scaffolds for adhesion and signaling in platelets.''; PubMed Europe PMC Scholia
  9. Kobilka BK, Matsui H, Kobilka TS, Yang-Feng TL, Francke U, Caron MG, Lefkowitz RJ, Regan JW.; ''Cloning, sequencing, and expression of the gene coding for the human platelet alpha 2-adrenergic receptor.''; PubMed Europe PMC Scholia
  10. Harburger DS, Calderwood DA.; ''Integrin signalling at a glance.''; PubMed Europe PMC Scholia
  11. Ruggeri ZM, Mendolicchio GL.; ''Adhesion mechanisms in platelet function.''; PubMed Europe PMC Scholia
  12. Ata R, Antonescu CN.; ''Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer.''; PubMed Europe PMC Scholia
  13. Butkowski RJ, Elion J, Downing MR, Mann KG.; ''Primary structure of human prethrombin 2 and alpha-thrombin.''; PubMed Europe PMC Scholia
  14. Shattil SJ.; ''Signaling through platelet integrin alpha IIb beta 3: inside-out, outside-in, and sideways.''; PubMed Europe PMC Scholia
  15. Parise LV.; ''Integrin alpha(IIb)beta(3) signaling in platelet adhesion and aggregation.''; PubMed Europe PMC Scholia
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  17. Watson SP, Auger JM, McCarty OJ, Pearce AC.; ''GPVI and integrin alphaIIb beta3 signaling in platelets.''; PubMed Europe PMC Scholia

History

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CompareRevisionActionTimeUserComment
114829view16:33, 25 January 2021ReactomeTeamReactome version 75
113275view11:34, 2 November 2020ReactomeTeamReactome version 74
112487view15:44, 9 October 2020ReactomeTeamReactome version 73
101399view11:28, 1 November 2018ReactomeTeamreactome version 66
100937view21:04, 31 October 2018ReactomeTeamreactome version 65
100474view19:38, 31 October 2018ReactomeTeamreactome version 64
100019view16:22, 31 October 2018ReactomeTeamreactome version 63
99572view14:54, 31 October 2018ReactomeTeamreactome version 62 (2nd attempt)
99195view12:43, 31 October 2018ReactomeTeamreactome version 62
94001view13:50, 16 August 2017ReactomeTeamreactome version 61
93611view11:28, 9 August 2017ReactomeTeamreactome version 61
88098view09:30, 26 July 2016RyanmillerOntology Term : 'homeostasis pathway' added !
88097view09:29, 26 July 2016RyanmillerOntology Term : 'regulatory pathway' added !
86719view09:24, 11 July 2016ReactomeTeamreactome version 56
83350view10:56, 18 November 2015ReactomeTeamVersion54
76986view08:27, 17 July 2014ReactomeTeamFixed remaining interactions
76691view12:05, 16 July 2014ReactomeTeamFixed remaining interactions
76017view10:07, 11 June 2014ReactomeTeamRe-fixing comment source
75726view11:19, 10 June 2014ReactomeTeamReactome 48 Update
75076view14:02, 8 May 2014AnweshaFixing comment source for displaying WikiPathways description
74723view08:48, 30 April 2014ReactomeTeamReactome46
42100view21:57, 4 March 2011MaintBotAutomatic update
39910view05:56, 21 January 2011MaintBotNew pathway

External references

DataNodes

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NameTypeDatabase referenceComment
Activated thrombin

(factor IIa)

ComplexREACT_3298 (Reactome)
Alpha-2

adrenoceptor

ProteinREACT_18048 (Reactome)
Alpha-2

adrenoceptor: Catecholamine

ComplexREACT_17529 (Reactome)
Catecholamine MetaboliteREACT_17411 (Reactome)
GP1b-IX-V

complex: activated thrombin (factor IIa)

ComplexREACT_24330 (Reactome)
GPIb-IX-V

complex

ComplexREACT_3007 (Reactome)
Integrin alphaIIb

beta3 signaling

PathwayREACT_15523 (Reactome) At the sites of vascular injury bioactive molecules such as thrombin, ADP, collagen, fibrinogen and thrombospondin are generated, secreted or exposed. These stimuli activate platelets, converting the major platelet integrin alphaIIbbeta3 from a resting state to an active conformation, in a process termed integrin priming or ‘inside-out signalling’. Integrin activation refers to the change required to enhance ligand-binding activity. The activated alphaIIbbeta3 interacts with the fibrinogen and links platelets together in an aggregate to form a platelet plug. AlphaIIbbeta3 bound to fibrin generates more intracellular signals (outside-in signalling), causing further platelet activation and platelet-plug retraction.
In the resting state the alpha and beta tails are close together. This interaction keeps the membrane proximal regions in a bent conformation that maintains alphaIIbbeta3 in a low affinity state.
Integrin alphaIIbbeta3 is released from its inactive state by interaction with the protein talin. Talin interacts with the beta3 cytoplasmic domain and disrupts the salt bridge between the alpha and beta chains. This separation in the cytoplasmic regions triggers the conformational change in the extracellular domain that increases its affinity to fibrinogen.
Much of talin exists in an inactive cytosolic pool, and the Rap1 interacting adaptor molecule (RIAM) is implicated in talin activation and translocation to beta3 integrin cytoplasmic domain.

Annotated Interactions

No annotated interactions

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