| First Author | Michalak M | Year | 1999 |
| Journal | Biochem J | Volume | 344 Pt 2 |
| Pages | 281-92 | PubMed ID | 10567207 |
| Mgi Jnum | J:58993 | Mgi Id | MGI:1350758 |
| Citation | Michalak M, et al. (1999) Calreticulin: one protein, one gene, many functions. Biochem J 344 Pt 2:281-92 |
| abstractText | 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 Ca(2+) 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 Ca(2+) 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 Ca(2+) homoeostasis by modulation of ER Ca(2+) 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. |
