Snare protein expression and adenoviral transfection of amphicrine AR42J

被引:15
作者
Gaisano, HY [1 ]
Huang, XH
Sheu, L
Ghai, M
Newgard, CB
Trinh, KY
Trimble, WS
机构
[1] Univ Toronto, Dept Med, Toronto, ON, Canada
[2] Univ Toronto, Dept Physiol, Toronto, ON, Canada
[3] Univ Toronto, Dept Biochem, Toronto, ON, Canada
[4] Hosp Sick Children, Cell Biol Program, Toronto Hosp, Toronto, ON M5S 1A8, Canada
[5] Univ SW Texas, Dallas, TX 75235 USA
基金
英国医学研究理事会;
关键词
D O I
10.1006/bbrc.1999.0987
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
The amphicrine AR42J acinar cell line is an excellent model to study both exocrine and neuroendocrine exocytotic mechanisms. As a first step toward this goal, we determined the specific isoforms of the v- and t-SNARE and Munc18 families expressed in these cells. In addition, we show that dexamethasone-induced differentiation toward the exocrine phenotype causes an upregulation of several of these proteins. AR42J is notoriously difficult to transfect, limiting its usefulness as a model. However, we have now overcome this obstacle by acheiving high efficiency expression of a beta-galactosidase reporter gene and truncated SNAP-25 gene using adenoviral infection techniques. The ARA2J cells can now be used to pursue and elucidate the distinct functions of individual SNARE isoforms used in endocrine and exocrine secretion within a single cell-line. (C) 1999 Academic Press.
引用
收藏
页码:781 / 784
页数:4
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