Open AccessPartial reprogramming strategy for intervertebral disc rejuvenation by activating energy switch
Author(s) -
Cheng Feng,
Wang Chenggui,
Ji Yufei,
Yang Biao,
Shu Jiawei,
Shi Kesi,
Wang Lulu,
Wang Shaoke,
Zhang Yuang,
Huang Xianpeng,
Zhou Xiaopeng,
Xia Kaishun,
Liang Chengzhen,
Chen Qixin,
Li Fangcai
Publication year - 2022
Publication title -
aging cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.103
H-Index - 140
eISSN - 1474-9726
pISSN - 1474-9718
DOI - 10.1111/acel.13577
Subject(s) - reprogramming , biology , klf4 , microbiology and biotechnology , sox2 , senescence , rejuvenation , cell , transcription factor , biochemistry , genetics , gene
Abstract Rejuvenation of nucleus pulposus cells (NPCs) in degenerative discs can reverse intervertebral disc degeneration (IDD). Partial reprogramming is used to rejuvenate aging cells and ameliorate progression of aging tissue to avoiding formation of tumors by classical reprogramming. Understanding the effects and potential mechanisms of partial reprogramming in degenerative discs provides insights for development of new therapies for IDD treatment. The findings of the present study show that partial reprogramming through short‐term cyclic expression of Oct‐3/4, Sox2, Klf4, and c‐Myc (OSKM) inhibits progression of IDD, and significantly reduces senescence related phenotypes in aging NPCs. Mechanistically, short‐term induction of OSKM in aging NPCs activates energy metabolism as a “energy switch” by upregulating expression of Hexokinase 2 (HK2) ultimately promoting redistribution of cytoskeleton and restoring the aging state in aging NPCs. These findings indicate that partial reprogramming through short‐term induction of OSKM has high therapeutic potential in the treatment of IDD.