| First Author | Jung EM | Year | 2020 |
| Journal | Cell Physiol Biochem | Volume | 54 |
| Issue | 3 | Pages | 438-456 |
| PubMed ID | 32357291 | Mgi Jnum | J:297878 |
| Mgi Id | MGI:6479362 | Doi | 10.33594/000000229 |
| Citation | Jung EM, et al. (2020) Calbindin-D9k is a Novel Risk Gene for Neurodegenerative Disease. Cell Physiol Biochem 54(3):438-456 |
| abstractText | BACKGROUND/AIMS: Calcium homeostasis plays a crucial role in neuronal development and disease. Calbindin-D9k (CaBP-9k) acts as calcium modulators and sensors in various tissues. However, the neurobiological functions of CaBP-9k are unknown. METHODS: We used CaBP-9k knockout (KO) mice to investigate the roles of these gene in neurodegenerative diseases, such as Alzheimer's and Parkinson's diseases. We used anatomical and biochemical approaches to characterize functional abnormalities of the brain in the CaBP-9k KO mice. RESULTS: We found that the brains of CaBP-9k KO mice have increased APP/beta-amyloid, Tau, and alpha-synuclein accumulation and endoplasmic reticulum (ER) stress-induced apoptosis. Neurons deficient for these CaBP-9k had abnormal intracellular calcium levels and responses. ER stress inhibitor TUDCA reduced ER stress-induced apoptosis and restored ER stress- and apoptosis-related proteins expression to wild-type levels in CaBP-9k KO mice. Furthermore, treatment with TUDCA rescued the abnormal memory and motor behaviors exhibited by older CaBP-9k KO mice. CONCLUSION: Our results suggest that a loss of CaBP-9k may contribute to the onset and progression of neurodegenerative diseases. |
