Mitochondrial outer membrane permeabilization

Mitochondrial outer membrane permeabilization (MOMP), also known as the mitochondrial outer membrane permeability, is one of two ways apoptosis (a type of programmed cell death) can be activated.[1] It is part of the intrinsic pathway of apoptosis, also known as the mitochondrial pathway. MOMP is known as the point of no return in apoptosis. Once triggered, it results in the diffusion of proteins from the space between the inner and outer mitochondrial membranes into the cytosol.[2]

Mechanism edit

Initiation of MOMP involves Bcl-2 family proteins, including BAX and BAK.[1] The outer mitochondrial membrane, typically permeable to molecules smaller than 5 kDa, forms pores during MOMP that allow it to accommodate proteins larger than 100 kDa. During MOMP, it takes about five minutes for all mitochondrial membranes within a cell to permeabilize.[3]

Outcome edit

MOMP has been referred to as the point of no return for apoptosis, almost always resulting in the completion of the process, and thus, cell death.[2] However, in limited circumstances, apoptosis does not complete. Sometimes, MOMP does not complete, known as incomplete MOMP (iMOMP) or minority MOMP (miniMOMP). For incomplete MOMP, mitochondrial membranes become permeable in most, but not all, the cell's mitochondria. In minority MOMP, only a few mitochondria of the cell experience MOMP—the result of sublethal stress.[3]

References edit

  1. ^ a b Fung, To Sing; Liu, Ding Xiang (2019). "Human Coronavirus: Host-Pathogen Interaction". Annual Review of Microbiology. 73: 529–557. doi:10.1146/annurev-micro-020518-115759. PMID 31226023.
  2. ^ a b Chipuk, J. E.; Bouchier-Hayes, L.; Green, D. R. (2006). "Mitochondrial outer membrane permeabilization during apoptosis: The innocent bystander scenario". Cell Death & Differentiation. 13 (8): 1396–1402. doi:10.1038/sj.cdd.4401963. PMID 16710362. S2CID 24464082.
  3. ^ a b Kalkavan, Halime; Green, Douglas R. (2018). "MOMP, cell suicide as a BCL-2 family business". Cell Death & Differentiation. 25 (1): 46–55. doi:10.1038/cdd.2017.179. PMC 5729535. PMID 29053143.