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Glycoprotein Ib

From Wikipedia, the free encyclopedia
Protein found in platelets

Glycoprotein Ib (GPIb), also known as CD42,[1]is a component of theGPIb-V-IX complex onplatelets. The GPIb-V-IX complex bindsvon Willebrand factor, allowingplatelet adhesion andplatelet plug formation at sites of vascular injury. Glycoprotein Ibα (GPIbα) is the major ligand-binding subunit of the GPIb-V-IX complex. GPIbα is heavily glycosylated.[2]

It is deficient in theBernard–Soulier syndrome. Again-of-function mutation causes platelet-typevon Willebrand disease.[3]

Autoantibodies against Ib/IX can be produced inimmune thrombocytopenic purpura.[4]

Components includeGP1BA andGP1BB.

It complexes withGlycoprotein IX.

References

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  1. ^Bode AP, Read MS, Reddick RL (February 1999). "Activation and adherence of lyophilized human platelets on canine vessel strips in the Baumgartner perfusion chamber".The Journal of Laboratory and Clinical Medicine.133 (2):200–211.doi:10.1016/S0022-2143(99)90013-6.PMID 9989772.
  2. ^Hollenhorst MA, Tiemeyer KH, Mahoney KE, Aoki K, Ishihara M, Lowery SC, et al. (April 2023)."Comprehensive analysis of platelet glycoprotein Ibα ectodomain glycosylation".Journal of Thrombosis and Haemostasis.21 (4):995–1009.doi:10.1016/j.jtha.2023.01.009.PMC 10065957.PMID 36740532.
  3. ^McPherson RA, Pincus MR (2007).Henry's Clinical Diagnosis and Management by Laboratory Methods (21st ed.). Philadelphia, Pa: Saunders Elsevier. pp. 760–762.ISBN 978-1-4160-0287-1.
  4. ^McMillan R (October 2007). "The pathogenesis of chronic immune thrombocytopenic purpura".Seminars in Hematology.44 (4 Suppl 5):S3 –S11.doi:10.1053/j.seminhematol.2007.11.002.PMID 18096470.

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Coagulation factors
Primary hemostasis
(platelet activation)
Intrinsic pathway
(contact activation)
Extrinsic pathway
(tissue factor)
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