Mitochondrial Heterogeneity in Stem Cells

被引:8
|
作者
Naik, Prajna Paramita [1 ,2 ]
Praharaj, Prakash P. [1 ]
Bhol, Chandra S. [1 ]
Panigrahi, Debasna P. [1 ]
Mahapatra, Kewal K. [1 ]
Patra, Srimanta [1 ]
Saha, Sarbari [1 ]
Bhutia, Sujit K. [1 ]
机构
[1] Natl Inst Technol Rourkela, Dept Life Sci, Rourkela, Odisha, India
[2] Vikram Deb Auto Coll, PG Dept Zool, Jeypore, Odisha, India
来源
关键词
Mitochondria; Stem cells; Mitochondrial heterogeneity; Embryonic development; ENERGY-METABOLISM; FISSION; FUSION; DIFFERENTIATION; MITOPHAGY; DYNAMICS; EMBRYO; ORGANIZATION; YEAST; INHERITANCE;
D O I
10.1007/978-3-030-11096-3_11
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondria are customarily acknowledged as the powerhouse of the cell by virtue of their indispensable role in cellular energy production. In addition, it plays an important role in pluripotency, differentiation, and reprogramming. This review describes variation in the stem cells and their mitochondrial heterogeneity. The mitochondrial variation can be described in terms of structure, function, and subcellular distribution. The mitochondria cristae development status and their localization patterns determine the oxygen consumption rate and ATP production which is a central controller of stem cell maintenance and differentiation. Generally, stem cells show spherical, immature mitochondria with perinuclear distribution. Such mitochondria are metabolically less energetic and low polarized. Moreover, mostly glycolytic energy production is found in pluripotent stem cells with a variation in naive stem cells which perform oxidative phosphorylation (OXPHOS). This article also describes the structural and functional journey of mitochondria during development. Future insight into underlying mechanisms associated with such alternation in mitochondria of stem cells during embryonic stages could uncover mitochondrial adaptability on cellular demands. Moreover, investigating the importance of mitochondria in pluripotency maintenance might unravel the cause of mitochondrial diseases, aging, and regenerative therapies.
引用
收藏
页码:179 / 194
页数:16
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