Department of Physiology, Yeungnam University College of Medicine, Daegu, Korea.
Cardiovascular and Metabolic Disease Center, Smart Marine Therapeutic Center, Department of Physiology, College of Medicine, Inje University, Busan, Korea.
Diabetes Metab J. 2021 Nov;45(6):853-865. doi: 10.4093/dmj.2021.0138. Epub 2021 Nov 22.
Tissues actively involved in energy metabolism are more likely to face metabolic challenges from bioenergetic substrates and are susceptible to mitochondrial dysfunction, leading to metabolic diseases. The mitochondria receive signals regarding the metabolic states in cells and transmit them to the nucleus or endoplasmic reticulum (ER) using calcium (Ca2+) for appropriate responses. Overflux of Ca2+ in the mitochondria or dysregulation of the signaling to the nucleus and ER could increase the incidence of metabolic diseases including insulin resistance and type 2 diabetes mellitus. Mitochondrial transcription factor A (Tfam) may regulate Ca2+ flux via changing the mitochondrial membrane potential and signals to other organelles such as the nucleus and ER. Since Tfam is involved in metabolic function in the mitochondria, here, we discuss the contribution of Tfam in coordinating mitochondria-ER activities for Ca2+ flux and describe the mechanisms by which Tfam affects mitochondrial Ca2+ flux in response to metabolic challenges.
组织积极参与能量代谢,因此更有可能面临生物能底物带来的代谢挑战,并且容易发生线粒体功能障碍,导致代谢疾病。线粒体接收关于细胞代谢状态的信号,并使用钙离子(Ca2+)将其传递到细胞核或内质网(ER),以做出适当的反应。线粒体中 Ca2+的过度流入或向细胞核和 ER 的信号转导失调,可能会增加包括胰岛素抵抗和 2 型糖尿病在内的代谢疾病的发病率。线粒体转录因子 A(Tfam)可以通过改变线粒体膜电位和向细胞核和 ER 等其他细胞器传递信号来调节 Ca2+流。由于 Tfam 参与线粒体的代谢功能,因此在这里,我们讨论了 Tfam 在协调线粒体-内质网活动以进行 Ca2+流中的作用,并描述了 Tfam 如何响应代谢挑战影响线粒体 Ca2+流的机制。