Wang Minghui, Lai Zhiwei, Zhang Hua, Yang Weiqi, Zheng Fengping, He Dehua, Liu Xiaofang, Zhong Rong, Qahar Mulan, Yang Guang
Division of Renal Medicine, Peking University Shenzhen Hospital, Peking University, Shenzhen, 518036, People's Republic of China.
Department of Burn and Plastic Surgery, Shenzhen Institute of Translational Medicine, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen, 518035, People's Republic of China.
J Inflamm Res. 2024 Sep 30;17:6781-6796. doi: 10.2147/JIR.S469239. eCollection 2024.
Diabetes mellitus (DM) is known to inhibit skin self-renewal and hair follicle stem cell (HFSC) activation, which may be key in the formation of chronic diabetic wounds. This study aimed to investigate the reasons behind the suppression of HFSC activation in DM mice.
Type 1 DM (T1DM) was induced in 6-week-old mice via streptozotocin, and hair follicle growth was subsequently monitored. RNA sequencing, bioinformatics analyses, qRT‒PCR, immunostaining, and cellular experiments were carried out to investigate the underlying mechanisms involved.
T1DM inhibited HFSC activation, which correlated with an increase in caspase-dependent programmed cell death. Additionally, T1DM triggered apoptosis and pyroptosis, predominantly in HFSCs and epidermal regions, with pyroptosis being more pronounced in the inner root sheath of hair follicles. Notably, significant cutaneous immune imbalances were observed, particularly in macrophages. Cellular experiments demonstrated that M1 macrophages inhibited HaCaT cell proliferation and induced cell death, whereas high-glucose environments alone did not have the same effect.
T1DM inhibits HFSC activation via macrophage reprogramming-mediated caspase-dependent pyroptosis, and there is a significant regional characterization of cell death. Moreover, T1DM-induced programmed cell death in the skin may be more closely related to immune homeostasis imbalance than to hyperglycemia itself. These findings shed light on the pathogenesis of diabetic ulcers and provide a theoretical basis for the use of hair follicle grafts in wound repair.
糖尿病(DM)已知会抑制皮肤自我更新和毛囊干细胞(HFSC)激活,这可能是慢性糖尿病伤口形成的关键因素。本研究旨在探究糖尿病小鼠中HFSC激活受抑制的原因。
通过链脲佐菌素诱导6周龄小鼠患1型糖尿病(T1DM),随后监测毛囊生长情况。进行RNA测序、生物信息学分析、qRT-PCR、免疫染色及细胞实验,以研究其中涉及的潜在机制。
T1DM抑制HFSC激活,这与半胱天冬酶依赖性程序性细胞死亡增加相关。此外,T1DM引发细胞凋亡和焦亡,主要发生在HFSCs和表皮区域,焦亡在毛囊内根鞘中更为明显。值得注意的是,观察到显著的皮肤免疫失衡,尤其是巨噬细胞方面。细胞实验表明,M1巨噬细胞抑制HaCaT细胞增殖并诱导细胞死亡,而单纯高糖环境则无此效果。
T1DM通过巨噬细胞重编程介导的半胱天冬酶依赖性焦亡抑制HFSC激活,且细胞死亡存在显著的区域特征。此外,T1DM诱导的皮肤程序性细胞死亡可能与免疫稳态失衡的关系比与高血糖本身的关系更为密切。这些发现为糖尿病溃疡的发病机制提供了新见解,并为在伤口修复中使用毛囊移植提供了理论依据。