Journal
THROMBOSIS AND HAEMOSTASIS
Volume 100, Issue 5, Pages 847-856Publisher
GEORG THIEME VERLAG KG
DOI: 10.1160/TH08-06-0351
Keywords
CIB1; platelet; integrin alpha IIb beta 3 activation; aggregation; knockout mouse; compensation
Categories
Funding
- NHLBI NIH HHS [P01 HL045100-100002, P01 HL045100-140001, P01 HL045100-130001, P01 HL045100, P01 HL045100-12, P01 HL045100-13, P01 HL045100-150001, P01 HL045100-070002, P01 HL045100-050002, P01 HL045100-080002, P01 HL045100-120001, P01 HL045100-06A10002, P01 HL045100-110001, P01 HL045100-090002, 2-P01-HL45100, R01 HL126124, P01 HL045100-15, P01 HL045100-14] Funding Source: Medline
Ask authors/readers for more resources
Platelet aggregation requires activation of the alpha IIb beta 3 integrin,an event regulated by the integrin cytoplasmic tails. CIB1 binds to the cytoplasmic tail of the integrin alpha IIb subunit. Previous overexpression and knockdown studies in murine megakaryocytes demonstrated that CIB1 inhibits integrin alpha IIb beta 3 activation. Here we analyzed Cib1(-/-) mice to determine the function of CIB1 in platelets in vitro and in vivo. We found that although these mice had no overt platelet phenotype, mRNA level of CIB1 homolog CIB3 was increased in Cib1(-/-) megakaryocytes. In vitro binding experiments showed that recombinant CIB1,-2 and -3 bound specifically to an allb cytoplasmic tail pepticle. Subsequent protein modeling experiments indicated that CIBs 1-3 each have a highly conserved hydrophobic binding pocket. Therefore, the potential exists for compensation for the loss of CIB1 by these CIB family members, thereby preventing pathologic thrombus formation in Cib1(-/-) mice.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available