» Articles » PMID: 33809551

The MAMs Structure and Its Role in Cell Death

Overview
Journal Cells
Publisher MDPI
Date 2021 Apr 3
PMID 33809551
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

The maintenance of cellular homeostasis involves the participation of multiple organelles. These organelles are associated in space and time, and either cooperate or antagonize each other with regards to cell function. Crosstalk between organelles has become a significant topic in research over recent decades. We believe that signal transduction between organelles, especially the endoplasmic reticulum (ER) and mitochondria, is a factor that can influence the cell fate. As the cellular center for protein folding and modification, the endoplasmic reticulum can influence a range of physiological processes by regulating the quantity and quality of proteins. Mitochondria, as the cellular "energy factory," are also involved in cell death processes. Some researchers regard the ER as the sensor of cellular stress and the mitochondria as an important actuator of the stress response. The scientific community now believe that bidirectional communication between the ER and the mitochondria can influence cell death. Recent studies revealed that the death signals can shuttle between the two organelles. Mitochondria-associated membranes (MAMs) play a vital role in the complex crosstalk between the ER and mitochondria. MAMs are known to play an important role in lipid synthesis, the regulation of Ca homeostasis, the coordination of ER-mitochondrial function, and the transduction of death signals between the ER and the mitochondria. Clarifying the structure and function of MAMs will provide new concepts for studying the pathological mechanisms associated with neurodegenerative diseases, aging, and cancers. Here, we review the recent studies of the structure and function of MAMs and its roles involved in cell death, especially in apoptosis.

Citing Articles

Mitochondria-associated endoplasmic reticulum membranes and myocardial ischemia: from molecular mechanisms to therapeutic strategies.

Chen C, Dai G, Fan M, Wang X, Niu K, Gao W J Transl Med. 2025; 23(1):277.

PMID: 40050915 PMC: 11884070. DOI: 10.1186/s12967-025-06262-3.


Endoplasmic Reticulum-Mitochondria Crosstalk in Fuchs Endothelial Corneal Dystrophy: Current Status and Future Prospects.

Kasi A, Steidl W, Kumar V Int J Mol Sci. 2025; 26(3).

PMID: 39940664 PMC: 11817211. DOI: 10.3390/ijms26030894.


Interaction Between the PERK/ATF4 Branch of the Endoplasmic Reticulum Stress and Mitochondrial One-Carbon Metabolism Regulates Neuronal Survival After Intracerebral Hemorrhage.

Liu Y, Cui F, Xu A, Wang B, Ma Y, Zhang Q Int J Biol Sci. 2024; 20(11):4277-4296.

PMID: 39247810 PMC: 11379068. DOI: 10.7150/ijbs.93787.


A promising anti-tumor targeting on ERMMDs mediated abnormal lipid metabolism in tumor cells.

Pang M, Yu L, Li X, Lu C, Xiao C, Liu Y Cell Death Dis. 2024; 15(8):562.

PMID: 39098929 PMC: 11298533. DOI: 10.1038/s41419-024-06956-4.


Targeting translocator protein protects against myocardial ischemia/reperfusion injury by alleviating mitochondrial dysfunction.

Wen C, Jiang Y, Chen W, Xu Y, Chen G, Zhou Q Exp Ther Med. 2024; 28(3):349.

PMID: 39071907 PMC: 11273255. DOI: 10.3892/etm.2024.12638.


References
1.
Friedman J, Lackner L, West M, Dibenedetto J, Nunnari J, Voeltz G . ER tubules mark sites of mitochondrial division. Science. 2011; 334(6054):358-62. PMC: 3366560. DOI: 10.1126/science.1207385. View

2.
Stoica R, De Vos K, Paillusson S, Mueller S, Sancho R, Lau K . ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43. Nat Commun. 2014; 5:3996. PMC: 4046113. DOI: 10.1038/ncomms4996. View

3.
Ivanova H, Vervliet T, Missiaen L, Parys J, De Smedt H, Bultynck G . Inositol 1,4,5-trisphosphate receptor-isoform diversity in cell death and survival. Biochim Biophys Acta. 2014; 1843(10):2164-83. DOI: 10.1016/j.bbamcr.2014.03.007. View

4.
Herrera-Cruz M, Simmen T . Over Six Decades of Discovery and Characterization of the Architecture at Mitochondria-Associated Membranes (MAMs). Adv Exp Med Biol. 2017; 997:13-31. DOI: 10.1007/978-981-10-4567-7_2. View

5.
Santucci R, Sinibaldi F, Cozza P, Polticelli F, Fiorucci L . Cytochrome c: An extreme multifunctional protein with a key role in cell fate. Int J Biol Macromol. 2019; 136:1237-1246. DOI: 10.1016/j.ijbiomac.2019.06.180. View