Injury-induced interleukin-1 alpha promotes Lgr5 hair follicle stem cells de novo regeneration and proliferation via regulating regenerative microenvironment in mice.

IF 5 3区 医学 Q2 IMMUNOLOGY
Guang Yang, Haiyan Chen, Qun Chen, Jiayi Qiu, Mulan Qahar, Zhimeng Fan, Weiwei Chu, Edward E Tredget, Yaojiong Wu
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引用次数: 6

Abstract

Background: The hair follicles (HFs) are barely regenerated after loss in injuries in mammals as well as in human beings. Recent studies have shown that the regenerative ability of HFs is age-related; however, the relationship between this phenomenon and the stem cell niche remains unclear. This study aimed to find a key secretory protein that promotes the HFs regeneration in the regenerative microenvironment.

Methods: To explore why age affects HFs de novo regeneration, we established an age-dependent HFs regeneration model in leucine-rich repeat G protein-coupled receptor 5 (Lgr5) + /mTmG mice. Proteins in tissue fluids were analyzed by high-throughput sequencing. The role and mechanism of candidate proteins in HFs de novo regeneration and hair follicle stem cells (HFSCs) activation were investigated through in vivo experiments. The effects of candidate proteins on skin cell populations were investigated by cellular experiments.

Results: Mice under 3-week-old (3W) could regenerate HFs and Lgr5 HFSCs, which were highly correlated with the immune cells, cytokines, IL-17 signaling pathway, and IL-1α level in the regeneration microenvironment. Additionally, IL-1α injection induced de novo regeneration of HFs and Lgr5 HFSCs in 3W mouse model with a 5 mm wound, as well as promoted activation and proliferation of Lgr5 HFSCs in 7-week-old (7W) mice without wound. Dexamethasone and TEMPOL inhibited the effects of IL-1α. Moreover, IL-1α increased skin thickness and promoted the proliferation of human epidermal keratinocyte line (HaCaT) and skin-derived precursors (SKPs) in vivo and in vitro, respectively.

Conclusions: In conclusion, injury-induced IL-1α promotes HFs regeneration by modulating inflammatory cells and oxidative stress-induced Lgr5 HFSCs regeneration as well as promoting skin cell populations proliferation. This study uncovers the underlying molecular mechanisms enabling HFs de novo regeneration in an age-dependent model.

Abstract Image

Abstract Image

Abstract Image

损伤诱导的白细胞介素-1 α通过调节小鼠再生微环境促进Lgr5毛囊干细胞新生再生和增殖。
研究背景:哺乳动物和人类的毛囊在损伤后几乎无法再生。最近的研究表明,HFs的再生能力与年龄有关;然而,这种现象与干细胞生态位之间的关系尚不清楚。本研究旨在寻找在再生微环境中促进HFs再生的关键分泌蛋白。方法:为了探究年龄影响hf新生再生的原因,我们在富亮氨酸重复G蛋白偶联受体5 (Lgr5) + /mTmG小鼠中建立了年龄依赖性hf再生模型。通过高通量测序分析组织液中的蛋白质。通过体内实验研究候选蛋白在HFs新生再生和毛囊干细胞(HFSCs)活化中的作用和机制。通过细胞实验研究了候选蛋白对皮肤细胞群的影响。结果:3周龄(3W)小鼠可再生HFs和Lgr5型HFSCs,其再生与再生微环境中的免疫细胞、细胞因子、IL-17信号通路和IL-1α水平高度相关。此外,IL-1α注射可诱导3W小鼠5 mm创伤模型中HFs和Lgr5 HFSCs的新生再生,并促进7周龄(7W)无创伤小鼠Lgr5 HFSCs的活化和增殖。地塞米松和TEMPOL抑制IL-1α的作用。此外,IL-1α在体内和体外分别增加皮肤厚度,促进人表皮角化细胞系(HaCaT)和皮肤源性前体(SKPs)的增殖。结论:损伤诱导的IL-1α通过调节炎症细胞和氧化应激诱导的Lgr5 HFSCs再生,促进皮肤细胞群增殖,促进HFs再生。这项研究揭示了在年龄依赖模型中使hf新生再生的潜在分子机制。
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来源期刊
CiteScore
11.10
自引率
1.20%
发文量
45
审稿时长
11 weeks
期刊介绍: Inflammation and Regeneration is the official journal of the Japanese Society of Inflammation and Regeneration (JSIR). This journal provides an open access forum which covers a wide range of scientific topics in the basic and clinical researches on inflammation and regenerative medicine. It also covers investigations of infectious diseases, including COVID-19 and other emerging infectious diseases, which involve the inflammatory responses. Inflammation and Regeneration publishes papers in the following categories: research article, note, rapid communication, case report, review and clinical drug evaluation.
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