CAS Key Laboratory of Tissue Microenvironment and Tumor, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, 200031, China.
School of Life Sciences, Shanghai University, Shanghai, 200444, China.
Adv Sci (Weinh). 2023 Feb;10(4):e2201949. doi: 10.1002/advs.202201949. Epub 2022 Dec 11.
Niche for stem cells profoundly influences their maintenance and fate during tissue homeostasis and pathological disorders; however, the underlying mechanisms and tissue-specific features remain poorly understood. Here, it is reported that fatty acid desaturation catabolized by stearoyl-coenzyme A desaturase 1 (SCD1) regulates hair follicle stem cells (HFSCs) and hair growth by maintaining the bulge, niche for HFSCs. Scd1 deletion in mice results in abnormal hair growth, an effect exerted directly on keratin K14 keratinocytes rather than on HFSCs. Mechanistically, Scd1 deficiency impairs the level of integrin α6β4 complex and thus the assembly of hemidesmosomes (HDs). The disruption of HDs allows the aberrant activation of focal adhesion kinase and PI3K in K14 keratinocytes and subsequently their differentiation and proliferation. The overgrowth of basal keratinocytes results in downward extension of the outer root sheath and interruption of bulge formation. Then, inhibition of PI3K signaling in Scd1 mice normalizes the bulge, HFSCs, and hair growth. Additionally, supplementation of oleic acid to Scd1 mice reestablishes HDs and the homeostasis of bulge niche, and restores hair growth. Thus, SCD1 is critical in regulating hair growth through stabilizing HDs in basal keratinocytes and thus sustaining bulge for HFSC residence and periodic activity.
干细胞所处的生态位对其在组织稳态和病理紊乱过程中的维持和命运具有深远影响;然而,其潜在机制和组织特异性特征仍知之甚少。本文报道了硬脂酰辅酶 A 去饱和酶 1(SCD1)通过脂肪酸去饱和作用来调节毛囊干细胞(HFSCs)和毛发生长,从而维持毛囊干细胞的隆突、生态位。在小鼠中敲除 Scd1 会导致异常的毛发生长,这一效应是直接作用于角蛋白 K14 角质形成细胞,而不是作用于 HFSCs。从机制上讲,Scd1 缺乏会损害整合素 α6β4 复合物的水平,从而影响半桥粒(HDs)的组装。HDs 的破坏会导致 K14 角质形成细胞中粘着斑激酶和 PI3K 的异常激活,随后角质形成细胞分化和增殖。基底角质形成细胞的过度生长导致外根鞘向下延伸,隆突形成中断。然后,抑制 Scd1 小鼠中的 PI3K 信号通路可使隆突、HFSCs 和毛发生长恢复正常。此外,向 Scd1 小鼠补充油酸可重建 HDs 和隆突生态位的稳态,并恢复毛发生长。因此,SCD1 通过稳定基底角质形成细胞中的 HDs 来调节毛发生长,从而维持 HFSC 定居和周期性活动的隆突。