Details

Autor(en) / Beteiligte

• Ni, Hong‐Min
• Baty, Catherine J.
• Li, Na
• Ding, Wen‐Xing
• Gao, Wentao
• Li, Min
• Chen, Xiaoyun
• Ma, Jianjie
• Michalopoulos, George K.
• Yin, Xiao‐Ming

Titel

Bid agonist regulates murine hepatocyte proliferation by controlling endoplasmic reticulum calcium homeostasis

Ist Teil von

• Hepatology (Baltimore, Md.), 2010-07, Vol.52 (1), p.338-348

Ort / Verlag

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

Erscheinungsjahr

2010

Quelle

Wiley Blackwell Single Titles

Beschreibungen/Notizen

• BH3‐interacting domain death agonist (Bid), a BH3‐only B cell lymphoma 2 family molecule, is generally known for its importance in activating the mitochondrial apoptosis pathway after death receptor engagement, particularly in hepatocytes. However, Bid also promotes hepatocyte proliferation during liver regeneration and carcinogenesis. This study was designed to examine the hypothesis that Bid regulates endoplasmic reticulum calcium concentration ([Ca2+]ER) homeostasis to affect hepatocyte proliferation. We found that serum‐stimulated hepatocyte proliferation was dependent on calcium, and the depletion of calcium with thapsigargin or ethylene glycol tetraacetic acid (EGTA) inhibited the proliferation. Subcellular fractionation showed that a portion of Bid was inserted into the endoplasmic reticulum (ER)–enriched membranes, and single‐cell calcium imaging indicated that Bid was important for maintaining the [Ca2+]ER level. Bid‐deficient hepatocytes manifested delayed and reduced serum‐stimulated proliferation, which was corrected by ionomycin or reconstitution of Bid, particularly an ER‐targeted Bid. Finally, B cell lymphoma 2–associated X protein (Bax) could also be found in the ER‐enriched membranes, and Bax deficiency caused the same proliferation defect. However, Bid/Bax double deletion in hepatocytes did not further augment the defect, which suggested that Bid and Bax worked by the same regulatory mechanism in [Ca2+]ER control. Conclusion: Bid regulates hepatocyte proliferation by positively affecting [Ca2+]ER homeostasis, and this could be important for liver regeneration and carcinogenesis. (HEPATOLOGY 2010)