Mitophagy Promotes Hair Regeneration by Activating Glutathione Metabolism.
Dehuan WangJingwei JiangMengyue WangKe LiHuan LiangNian'ou WangWeiwei LiuMiaomiao WangSiyi ZhouMan ZhangYang XiaoXinyu ShenZeming LiWang WuXia LinXiao XiangQiaoli XieWanqian LiuXun ZhouQu TangWei ZhouLi YangCheng-Ming ChuongMingxing LeiPublished in: Research (Washington, D.C.) (2024)
Mitophagy maintains tissue homeostasis by self-eliminating defective mitochondria through autophagy. How mitophagy regulates stem cell activity during hair regeneration remains unclear. Here, we found that mitophagy promotes the proliferation of hair germ (HG) cells by regulating glutathione (GSH) metabolism. First, single-cell RNA sequencing, mitochondrial probe, transmission electron microscopy, and immunofluorescence staining showed stronger mitochondrial activity and increased mitophagy-related gene especially Prohibitin 2 (Phb2) expression at early-anagen HG compared to the telogen HG. Mitochondrial inner membrane receptor protein PHB2 binds to LC3 to initiate mitophagy. Second, molecular docking and functional studies revealed that PHB2-LC3 activates mitophagy to eliminate the damaged mitochondria in HG. RNA-seq, single-cell metabolism, immunofluorescence staining, and functional validation discovered that LC3 promotes GSH metabolism to supply energy for promoting HG proliferation. Third, transcriptomics analysis and immunofluorescence staining indicated that mitophagy was down-regulated in the aged compared to young-mouse HG. Activating mitophagy and GSH pathways through small-molecule administration can reactivate HG cell proliferation followed by hair regeneration in aged hair follicles. Our findings open up a new avenue for exploring autophagy that promotes hair regeneration and emphasizes the role of the self-elimination effect of mitophagy in controlling the proliferation of HG cells by regulating GSH metabolism.
Keyphrases
- single cell
- fluorescent probe
- rna seq
- stem cells
- living cells
- signaling pathway
- nlrp inflammasome
- oxidative stress
- small molecule
- induced apoptosis
- molecular docking
- cell death
- cell proliferation
- aqueous solution
- high throughput
- cell cycle arrest
- endoplasmic reticulum stress
- pi k akt
- mass spectrometry
- gene expression
- minimally invasive
- genome wide
- wound healing
- high resolution
- transcription factor
- liquid chromatography
- flow cytometry
- binding protein
- drug induced