Cloning and localization of Rab3 isoforms in bovine, rat, and human parathyroid glands

Citation
Zm. Huang et al., Cloning and localization of Rab3 isoforms in bovine, rat, and human parathyroid glands, BIOC BIOP R, 255(3), 1999, pp. 645-651
Citations number
50
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
255
Issue
3
Year of publication
1999
Pages
645 - 651
Database
ISI
SICI code
0006-291X(19990224)255:3<645:CALORI>2.0.ZU;2-F
Abstract
Rab3 proteins are small GTP-binding proteins known to play a role in regula ted exocytosis processes. This study examines the expression of Rab3 mRNA a nd protein in bovine, rat and human parathyroid glands. mRNAs of several Ra b3 isoforms were detected in bovine (Rab3A, Rab3B and Rab3C) and rat (Rab3A , Rab3B and Rab3D) parathyroid glands by RT-PCR and sequencing. Rab3A prote in was detected in the cytosolic extract from bovine parathyroid gland by W estern blotting using a monoclonal antibody for Rab3A. Rab3A protein was lo calized to parathyroid hormone-containing chief cells by immunohistochemica l staining. Subcellular localization of Rab3A protein by immunogold electro n microscopy revealed that the majority of Rab3A protein was not associated with dense-core vesicles, but localized in the cytosol of the chief cells. Altogether, our results demonstrate that Rab3 isoforms are expressed in pa rathyroid chief cells, suggesting that they may play a role in regulated ex ocytosis in these cells. (C) 1999 Academic Press.