Expression pattern of alternatively spliced PECAM-1 isoforms in hematopoietic cells and platelets

被引:36
|
作者
Wang, YJ
Sheibani, N
机构
[1] Univ Wisconsin, Sch Med, Dept Ophthalmol & Visual Sci, Madison, WI 53792 USA
[2] Univ Wisconsin, Sch Med, Dept Pharmacol, Madison, WI 53792 USA
关键词
CD31; alternative splicing; angiogenesis; adherens junctions; cell-cell interactions;
D O I
10.1002/jcb.10321
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PECAM-1 (CD31) is a cell adhesion molecule that is highly expressed in the endothelium. Hematopoietic cells including platelets, monocytes, neutrophils, and some T cells also express moderate levels of PECAM-1. PECAM-1 undergoes alternative splicing generating a number of isoforms in the endothelium. However, the expression of PECAM-1 isoforms in hematopoietic cells and platelets has not been determined. Here, we examined the expression pattern of PECAM-1 isoforms inhuman and rodent hematopoietic cells and platelets by RT-PCR and DNA sequencing analysis. Our results showed that multiple PECAM-1 isoforms are expressed in a cell-type and species-specific pattern. We identified seven human PECAM-1 isoforms, six murine PECAM-1 isoforms, and four rat PECAM-1 isoforms. The full-length PECAM-1 was the predominant isoform detected in human cells. The PECAM-1 isoforms that lack exon 14 and 15 (Delta1415) or Delta12,14&15 were the predominant isoform in rodent cells. In addition, we identified a novel PECAM-1 isoform, Delta13&14, inhuman hematopoietic cells. Thus, hematopoietic cells express multiple isoforms of PECAM-1 in a pattern similar to that observed in the endothelium of the same species. The regulated expression of these isoforms may be important during hematopoiesis and transendothelial migration.
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页码:424 / 438
页数:15
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