Spatiotemporal Ca²⁺ Nanodomain Remodeling at MERCS Regulates Mitochondrial Proteostasis
en-GBde-DEes-ESfr-FR

Spatiotemporal Ca²⁺ Nanodomain Remodeling at MERCS Regulates Mitochondrial Proteostasis

22/02/2026 Frontiers Journals

In November 2025, a team led by Dr. Yuting Guo at the University of Chinese Academy of Sciences revealed how mitochondria-ER contact sites (MERCS) decode proteotoxic stress via calcium nanodomain regulation, activating adaptive mitochondrial responses. Published in Protein & Cell, the work proposes new therapeutic avenues for neurodegenerative diseases.
Mitochondrial proteostasis disruption contributes critically to aging and disease. The mitochondrial unfolded protein response (UPRmt), a conserved pathway from C. elegans to primates, restores proteostasis by inducing chaperones and proteases. However, its complex regulation and technical limitations in live-cell imaging have left mammalian UPRmt activation mechanisms poorly understood. Moreover, while mitochondrial calcium dynamics is central to mitochondrial homeostasis, its spatiotemporal link to UPRmt remain unclear.
To address these questions, the team employed their home-made high-resolution GI/3D-SIM imaging technology and constructed MERCS-enhanced (REDMAP) and -deficient models. They found that enhanced MERCS restrict mitochondrial calcium efflux, delay mPTP opening, and subsequently activate UPRmt.
Mechanistically, MERCS-mediated calcium retention triggers UPRmt via two pathways: 1) Impaired calcium efflux reduces ATF5 mitochondrial import, promoting its nuclear translocation and stress gene expression; and 2) Calcium-sensitive kinase CAMK4 drives H3K27 acetylation, increasing chromatin accessibility and UPRmt transcription.
In an Alzheimer’s model, this “calcium-transcription-epigenetics” axis conferred neuroprotection. Inhibiting mPTP pharmacologically (CsA) or genetically (CypD-KD) activated UPRmt, alleviating Aβ-induced mitochondrial dysfunction and apoptosis.
This study systematically elucidates how MERCS-regulated nanocalcium signals integrate transcriptional and epigenetic mechanisms to preserve proteostasis, advancing inter-organelle communication understanding and identifying new targets for diseases like AD.
The research was conducted at the University of Chinese Academy of Sciences. Co-first authors are Dr. Lv Yanan, MSc Zhao Xuejing, and Prof. Li Di. Corresponding author is Prof. Guo Yuting.
DOI:10.1093/procel/pwaf097
Fichiers joints
  • Working model for calcium-mediated UPRmt activation. Schematic illustration showing the role of Ca2+ transients in the protective of AD cells against apoptosis
22/02/2026 Frontiers Journals
Regions: Asia, China
Keywords: Science, Life Sciences

Disclaimer: AlphaGalileo is not responsible for the accuracy of content posted to AlphaGalileo by contributing institutions or for the use of any information through the AlphaGalileo system.

Témoignages

We have used AlphaGalileo since its foundation but frankly we need it more than ever now to ensure our research news is heard across Europe, Asia and North America. As one of the UK’s leading research universities we want to continue to work with other outstanding researchers in Europe. AlphaGalileo helps us to continue to bring our research story to them and the rest of the world.
Peter Dunn, Director of Press and Media Relations at the University of Warwick
AlphaGalileo has helped us more than double our reach at SciDev.Net. The service has enabled our journalists around the world to reach the mainstream media with articles about the impact of science on people in low- and middle-income countries, leading to big increases in the number of SciDev.Net articles that have been republished.
Ben Deighton, SciDevNet
AlphaGalileo is a great source of global research news. I use it regularly.
Robert Lee Hotz, LA Times

Nous travaillons en étroite collaboration avec...


  • e
  • The Research Council of Norway
  • SciDevNet
  • Swiss National Science Foundation
  • iesResearch
Copyright 2026 by DNN Corp Terms Of Use Privacy Statement