| Literature DB >> 19105223 |
Mohamad Azhar1, Moying Yin, Ming Zhou, Hongqi Li, Marwan Mustafa, Eyad Nusayr, Jack B Keenan, Hwudaurw Chen, Sharon Pawlosky, Connie Gard, Christina Grisham, L Philip Sanford, Tom Doetschman.
Abstract
Fibroblast growth factor-2 (FGF2) is produced as high molecular weight isoforms (HMW) and a low molecular weight isoform (LMW) by means of alternative usage of translation start sites in a single Fgf2 mRNA. Although the physiological function of FGF2 and FGF2 LMW has been investigated in myocardial capillarogenesis during normal cardiac growth, the role of FGF2 HMW has not been determined. Here, we report the generation of FGF2 HMW-deficient mice in which FGF2 HMW isoforms are ablated by the Tag-and-Exchange gene targeting technique. These mice are normal and fertile with normal fecundity, and have a normal life span. Histological, immunohistochemical, and morphometric analyses indicate normal myocardial architecture, blood vessel, and cardiac capillary density in young adult FGF2 HMW-deficient mice. These mice along with the FGF2- and FGF2 LMW-deficient mice that we have generated previously will be very useful for elucidating the differential functions of FGF2 isoforms in pathophysiology of cardiovascular diseases.Entities:
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Year: 2009 PMID: 19105223 PMCID: PMC2649784 DOI: 10.1002/dvdy.21835
Source DB: PubMed Journal: Dev Dyn ISSN: 1058-8388 Impact factor: 3.780