Yoshigai Emi, Hara Takafumi, Hashimoto Masaki, Tsuzuki Hidenao, Abe Takaya, Inoue Kenichi, Noguchi Ayaka, Ohashi Takuto, Fukada Toshiyuki
Molecular and Cellular Physiology, Faculty of Pharmaceutical Sciences, Tokushima Bunri University, 180 Nishihama-Boji, Yamashiro, Tokushima, 770-8514, Japan.
JSPS Research Fellowship for Young Scientists, Tokyo, Japan.
Sci Rep. 2025 Mar 17;15(1):9206. doi: 10.1038/s41598-025-92501-y.
Loss of ZIP13 causes Ehlers-Danlos syndrome spondylodysplastic type 3 involving connective tissue dysplasias associated with a reduction in muscular strength. However, ZIP13 role in skeletal muscle homeostasis, particularly for the regulation of muscle satellite cells (MuSCs), remains poorly understood. In this study, we investigated Zip13-knockout (KO) mice and found a reduction in MuSCs of Zip13-KO mice, in which the quiescent and activated phase balances were disrupted. To clarify the physiological role and dynamics of ZIP13 expression in MuSCs, we generated Zip13-GFP knock-in (KI) mice encoding GFP at the Zip13 locus, which showed that ZIP13 contributes to the phase balance regulation of quiescent and activated MuSCs and their functions. Indeed, Zip13-KO mice exhibited delayed recovery from skeletal muscle injury, indicating ZIP13 requirement for proper skeletal muscle regeneration. Moreover, GFP expression was reduced in the MuSCs of homozygous Zip13-GFP KI mice whose intact ZIP13 expression was perturbed, suggesting that positive feedback mechanisms exist to maintain ZIP13 expression. Altogether, our results illustrate that ZIP13 might be positively involved in skeletal muscle regeneration by controlling the quiescent/activated phase balance of MuSCs through autoregulatory ZIP13 expression, and that newly generated Zip13-GFP KI mice would be useful for investigating the roles and dynamics of ZIP13-expressing cells.
ZIP13的缺失会导致3型脊椎发育不良型埃勒斯-当洛综合征,其涉及与肌肉力量降低相关的结缔组织发育异常。然而,ZIP13在骨骼肌稳态中的作用,尤其是对肌肉卫星细胞(MuSCs)的调节作用,仍知之甚少。在本研究中,我们对Zip13基因敲除(KO)小鼠进行了研究,发现Zip13-KO小鼠的MuSCs数量减少,其静止期和激活期的平衡被打破。为了阐明ZIP13在MuSCs中的生理作用和表达动态,我们构建了在Zip13基因座编码绿色荧光蛋白(GFP)的Zip13-GFP基因敲入(KI)小鼠,结果表明ZIP13有助于静止期和激活期MuSCs的平衡调节及其功能。实际上,Zip13-KO小鼠骨骼肌损伤后的恢复延迟,表明骨骼肌正常再生需要ZIP13。此外,在完整ZIP13表达受到干扰的纯合Zip13-GFP KI小鼠的MuSCs中,GFP表达降低,这表明存在维持ZIP13表达的正反馈机制。总之,我们的结果表明,ZIP13可能通过自动调节ZIP13的表达来控制MuSCs的静止/激活期平衡,从而积极参与骨骼肌再生,并且新构建的Zip13-GFP KI小鼠将有助于研究ZIP13表达细胞的作用和动态。