Calreticulin: one protein, one gene, many functions

被引:680
作者
Michalak, M
Corbett, EF
Mesaeli, N
Nakamura, K
Opas, M
机构
[1] Univ Alberta, MRC Grp Mol Biol Membranes, Edmonton, AB T6G 2H7, Canada
[2] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
[3] Univ Toronto, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, Canada
关键词
Ca2+ homoeostasis; chaperoning; endoplasmic reticulum; luminal resident protein; membranes;
D O I
10.1042/0264-6021:3440281
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 endoplasmic reticulum (ER) plays a critical role in the synthesis and chaperoning of membrane-associated and secreted proteins. The membrane is also an important site of Ca2+ storage and release. Calreticulin is a unique ER luminal resident protein. The protein affects many cellular functions, both in the ER lumen and outside of the ER environment. In the ER lumen, calreticulin performs two major functions: chaperoning and regulation of Ca2+ homoeostasis. Calreticulin is a highly versatile lectin-like chaperone, and it participates during the synthesis of a variety of molecules, including ion channels, surface receptors, integrins and transporters. The protein also affects intracellular Ca2+ homoeostasis by modulation of ER Ca2+ storage and transport. Studies on the cell biology of calreticulin revealed that the ER membrane is a very dynamic intracellular compartment affecting many aspects of cell physiology.
引用
收藏
页码:281 / 292
页数:12
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