M2 microglia-derived exosomes reduce neuronal ferroptosis via FUNDC1-mediated mitophagy by activating AMPK/ULK1 signaling
Abstract Neuronal ferroptosis plays a vital role in the progression of neonatal hypoxic-ischemic brain damage (HIBD). M2-type microglia-derived exosomes (M2-exos) have been shown to protect neurons from ischemia–reperfusion (I/R) brain injury, but their impact on I/R-induced neuronal ferroptosis and...
Saved in:
| Main Authors: | Jian Li, Qing Chen, Hao Gu |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-05-01
|
| Series: | Scientific Reports |
| Subjects: | |
| Online Access: | https://doi.org/10.1038/s41598-025-03091-8 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Mechanisms Associated with Mitophagy and Ferroptosis in Cerebral Ischemia-reperfusion Injury
by: Yugang Ma, et al.
Published: (2025-03-01) -
Artesunate alleviates cerebral ischemia/reperfusion injury by suppressing FUNDC1-mediated excessive mitophagy
by: Fei Wang, et al.
Published: (2025-08-01) -
Exosomal circ_0093708 as a potential ferroptosis biomarker in cerebral ischemia–reperfusion injury
by: Shuyin Ma, et al.
Published: (2025-08-01) -
Advances in the Study of Mitophagy in Renal Ischemia–Reperfusion Injury
by: Rumeng Li, et al.
Published: (2025-04-01) -
The UCP2/PINK1/LC3b-mediated mitophagy is involved in the protection of NRG1 against myocardial ischemia/reperfusion injury
by: Xin-Tao Li, et al.
Published: (2025-03-01)