Department of Cell Biology, University of Alabama at Birmingham Medical School, Birmingham, AL 35294, USA.
Development. 2011 May;138(9):1675-85. doi: 10.1242/dev.060210. Epub 2011 Mar 23.
Skin and hair follicle morphogenesis and homeostasis require the integration of multiple signaling pathways, including Hedgehog (Hh) and Wingless (Wnt), and oriented cell divisions, all of which have been associated with primary cilia. Although studies have shown that disrupting dermal cilia causes follicular arrest and attenuated Hh signaling, little is known about the role of epidermal cilia. Here, epidermal cilia function was analyzed using conditional alleles of the ciliogenic genes Ift88 and Kif3a. At birth, epidermal cilia mutants appeared normal, but developed basaloid hyperplasia and ingrowths into the dermis of the ventrum with age. In addition, follicles in the tail were disorganized and had excess sebaceous gland lobules. Epidermal cilia mutants displayed fewer long-term label-retaining cells, suggesting altered stem cell homeostasis. Abnormal proliferation and differentiation were evident from lineage-tracing studies and showed an expansion of follicular cells into the interfollicular epidermis, as is seen during wound repair. These phenotypes were not associated with changes in canonical Wnt activity or oriented cell division. However, nuclear accumulation of the ΔNp63 transcription factor, which is involved in stratification, keratinocyte differentiation and wound repair, was increased, whereas the Hh pathway was repressed. Intriguingly, the phenotypes were not typical of those associated with loss of Hh signaling but exhibited similarities with those of mice in which ΔNp63 is overexpressed in the epidermis. Collectively, these data indicate that epidermal primary cilia may function in stress responses and epidermal homeostasis involving pathways other than those typically associated with primary cilia.
皮肤和毛囊的形态发生和动态平衡需要多种信号通路的整合,包括 Hedgehog(Hh)和 Wingless(Wnt),以及定向细胞分裂,所有这些都与初级纤毛有关。虽然研究表明,破坏真皮纤毛会导致毛囊停滞和减弱的 Hh 信号,但表皮纤毛的作用知之甚少。在这里,使用纤毛生成基因 Ift88 和 Kif3a 的条件等位基因分析了表皮纤毛的功能。在出生时,表皮纤毛突变体看起来正常,但随着年龄的增长,会出现基底细胞增生和向腹部真皮内生长。此外,尾巴上的毛囊排列紊乱,皮脂腺小叶过多。表皮纤毛突变体显示出较少的长期标记保留细胞,表明干细胞动态平衡发生改变。谱系追踪研究显示出异常的增殖和分化,表明毛囊细胞扩张进入滤泡间表皮,这类似于伤口修复过程中的情况。这些表型与经典 Wnt 活性或定向细胞分裂的变化无关。然而,参与分层、角质形成细胞分化和伤口修复的 ΔNp63 转录因子的核积累增加,而 Hh 途径受到抑制。有趣的是,这些表型与典型的 Hh 信号缺失相关的表型不同,但与表皮中 ΔNp63 过表达的小鼠的表型相似。总的来说,这些数据表明表皮初级纤毛可能在涉及与初级纤毛通常相关的途径以外的应激反应和表皮动态平衡中发挥作用。