講座主題：線粒體內(nèi)膜的CALHM2孔道：細(xì)胞代謝調(diào)控新機(jī)制
專家姓名：王世強(qiáng)
工作單位：北京大學(xué)
講座時(shí)間：2024年10月18日13:30-14:30
講座地點(diǎn)：八角灣校區(qū)行政樓報(bào)告廳
主辦單位：煙臺(tái)大學(xué)生命科學(xué)學(xué)院
內(nèi)容摘要：
The calcium homeostasis modulator (CALHM)-2 is a member of the CALHM gene family residing at 10q24.33 of human genome, but its function is yet unknown. We found that CALHM2 forms a mega channel in the inner membrane of mitochondria. CALHM2 channels are opened by ATP and closed by Ca2+. Opened CALHM2 channels are permeable to molecules like ATP and induce fluctuations of mitochondrial membrane potential. CALHM2 knockdown/knockout decreases cytosolic ATP concentration, and thereby compromises energy-sensitive processes, such as intracellular Ca2+ handling. However, CALHM2 loss-of-function elevates ATP concentration in the mitochondrial matrix, dephosphorylates key enzymes in the mammalian target of rapamycin (mTOR) pathway, and promotes longevity in CALHM2 knockout mice. These findings reveal that CALHM2 constitutes a novel regulator of mitochondrial metabolism, which may has important implications in aging and diseases.
主講人介紹：
王世強(qiáng)，北京大學(xué)生命科學(xué)學(xué)院長(zhǎng)江學(xué)者特聘教授，國(guó)家杰出青年科學(xué)基金獲得者,，國(guó)家“萬(wàn)人計(jì)劃”領(lǐng)軍人才,。長(zhǎng)期從事細(xì)胞鈣信號(hào)轉(zhuǎn)導(dǎo)研究，從分子間相互作用的角度闡明心肌細(xì)胞興奮收縮耦聯(lián)的分子機(jī)制，系統(tǒng)研究了心肌肥厚、心力衰竭、心律失常的心臟疾病條件下興奮收縮耦聯(lián)的結(jié)構(gòu)和功能重塑,，闡明其中鈣信號(hào)、microRNA,、相關(guān)蛋白及其啟動(dòng)子和轉(zhuǎn)錄因子的病理變化規(guī)律,，提出治療或逆轉(zhuǎn)這些病理過(guò)程的新理論。先后承擔(dān)“973”計(jì)劃,、“863”計(jì)劃,、國(guó)家重點(diǎn)研發(fā)計(jì)劃，以及國(guó)家自然科學(xué)基金重點(diǎn)項(xiàng)目,、重大研究計(jì)劃等科研項(xiàng)目,，系列重要成果發(fā)表于Nature、Circulation Research,、PNAS等期刊,，曾獲北京市優(yōu)秀教師、全國(guó)優(yōu)秀科技工作者,、國(guó)家級(jí)一流本科課程,、教育部自然科學(xué)一等獎(jiǎng)、國(guó)家自然科學(xué)二等獎(jiǎng),、國(guó)務(wù)院政府特殊津貼等榮譽(yù),。
