| First Author | Nguyen DT | Year | 2021 |
| Journal | Sci Rep | Volume | 11 |
| Issue | 1 | Pages | 13086 |
| PubMed ID | 34158584 | Mgi Jnum | J:343850 |
| Mgi Id | MGI:6720187 | Doi | 10.1038/s41598-021-92529-w |
| Citation | Nguyen DT, et al. (2021) The ATF6beta-calreticulin axis promotes neuronal survival under endoplasmic reticulum stress and excitotoxicity. Sci Rep 11(1):13086 |
| abstractText | While ATF6alpha plays a central role in the endoplasmic reticulum (ER) stress response, the function of its paralogue ATF6beta remains elusive, especially in the central nervous system (CNS). Here, we demonstrate that ATF6beta is highly expressed in the hippocampus of the brain, and specifically regulates the expression of calreticulin (CRT), a molecular chaperone in the ER with a high Ca(2+)-binding capacity. CRT expression was reduced to ~ 50% in the CNS of Atf6b(-/-) mice under both normal and ER stress conditions. Analysis using cultured hippocampal neurons revealed that ATF6beta deficiency reduced Ca(2+) stores in the ER and enhanced ER stress-induced death. The higher levels of death in Atf6b(-/-) neurons were recovered by ATF6beta and CRT overexpressions, or by treatment with Ca(2+)-modulating reagents such as BAPTA-AM and 2-APB, and with an ER stress inhibitor salubrinal. In vivo, kainate-induced neuronal death was enhanced in the hippocampi of Atf6b(-/-) and Calr(+/-) mice, and restored by administration of 2-APB and salubrinal. These results suggest that the ATF6beta-CRT axis promotes neuronal survival under ER stress and excitotoxity by improving intracellular Ca(2+) homeostasis. |
