The role of mitochondrial-associated endoplasmic reticulum membranes (MAMs) in diabetic microvascular complications:

Yudian Wang1, Yufei Zhang1, Qi Jin2

  • 1College of Traditional Chinese Medicine, Hubei University of Chinese Medicine, Hubei, Wuhan, China.

Cell Death & Disease
|December 9, 2025
PubMed

Insights

Mitochondria-associated endoplasmic reticulum membranes (MAMs) regulate key processes implicated in diabetic microvascular complications. Targeting MAMs offers a potential therapeutic strategy for conditions like diabetic kidney disease, cardiomyopathy, and retinopathy.

Area of Science:

  • Cell Biology
  • Endocrinology
  • Pathophysiology

Background:

  • Diabetic microvascular complications (DMC) involve endothelial dysfunction and damage to kidneys, heart, eyes, and peripheral systems.
  • Mitochondria-associated endoplasmic reticulum membranes (MAMs) are crucial for inter-organelle communication, impacting cellular homeostasis.

Purpose of the Study:

  • To comprehensively review the structure and function of MAMs in the context of diabetic microvascular complications.
  • To explore the regulatory mechanisms of MAMs in diabetic kidney disease, cardiomyopathy, and retinopathy.

Main Methods:

  • Literature review of studies investigating MAMs and diabetic microvascular complications.
  • Synthesis of current knowledge on MAMs' role in calcium homeostasis, lipid metabolism, mitochondrial dynamics, ER stress, and inflammation.

Main Results:

  • MAMs are implicated in the pathogenesis of DMC through regulation of Ca2+ homeostasis, lipid synthesis, mitochondrial dynamics, ER stress, glucose homeostasis, autophagy, apoptosis, and inflammation.
  • Dysregulation of MAMs contributes to diabetic kidney disease (DKD), diabetic cardiomyopathy (DCM), and diabetic retinopathy (DR).

Conclusions:

  • MAMs play a significant role in the development and progression of diabetic microvascular complications.
  • Targeting MAMs presents a promising yet challenging therapeutic avenue for managing DMC and its associated organ damage.

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