Department of Dermatology, Hamamatsu University School of Medicine, Japan.
Department of Dermatology, Hamamatsu University School of Medicine, Japan.
J Dermatol Sci. 2018 Sep;91(3):250-255. doi: 10.1016/j.jdermsci.2018.05.004. Epub 2018 May 12.
De novo hair regeneration occurs in scars of normal adult mice. This interesting phenomenon is termed as wound-induced hair neogenesis (WIHN). We hypothesized that M2 macrophages are crucially involved in WIHN.
To clarify the contribution of M2 macrophages to WIHN.
We established a mouse model of WIHN. A full thickness skin excision was implemented on the back of C57BL/6 (B6) mice. Newly developing hair follicles were detected by a whole-mount assay. WIHN took place 2 weeks after wounding.
At first, flow cytometry revealed increased infiltration of CD11b/CD206 M2 macrophages at the 2nd and 3rd week after wounding. Immunohistochemistry also showed the existence of CD206 M2 macrophages in the vicinity of regenerated hair follicles. Secondly, the productions of growth factors were confirmed by culturing M2 macrophages isolated from the skin in a comparison with CD11b spleen cells. Array for 84 genes revealed increased expressions of various growth factors including Igf1 and Fgf2. Thirdly, we verified the effect of the growth factors on WIHN. WIHN was increased by 2 folds in mice treated with Fgf2 (p=0.05) or by 1.5 folds with Igf1 (p=0.05). Finally, we used B6.Tg(ITGAM-DTR) mice in which macrophages are ablated by diphtheria toxin. We depleted macrophages at one to 2 weeks after wounding when M2 macrophages were dominant. WIHN was attenuated to one third (P=0.05) by the ablation of macrophages.
Our study suggests that M2 macrophages could promote WIHN through producing a panel of growth factors.
新生毛发再生发生在正常成年小鼠的疤痕中。这种有趣的现象被称为创伤诱导的毛发新生(WIHN)。我们假设 M2 巨噬细胞在 WIHN 中起着至关重要的作用。
阐明 M2 巨噬细胞对 WIHN 的贡献。
我们建立了 WIHN 的小鼠模型。在 C57BL/6(B6)小鼠的背部进行全层皮肤切除。通过全距测定法检测新发育的毛囊。创伤后 2 周发生 WIHN。
首先,流式细胞术显示,在创伤后第 2 周和第 3 周,CD11b/CD206 M2 巨噬细胞的浸润增加。免疫组织化学也显示 CD206 M2 巨噬细胞存在于再生毛囊附近。其次,通过将从皮肤中分离的 M2 巨噬细胞与 CD11b 脾细胞进行培养,证实了生长因子的产生。84 个基因的阵列显示出各种生长因子(包括 Igf1 和 Fgf2)的表达增加。第三,我们验证了生长因子对 WIHN 的影响。用 Fgf2(p=0.05)或 Igf1(p=0.05)处理的小鼠,WIHN 增加了 2 倍。最后,我们使用 B6.Tg(ITGAM-DTR) 小鼠,其中巨噬细胞通过白喉毒素被消除。我们在创伤后 1 至 2 周时耗尽巨噬细胞,此时 M2 巨噬细胞占主导地位。巨噬细胞的耗竭使 WIHN 减弱到三分之一(P=0.05)。
我们的研究表明,M2 巨噬细胞可以通过产生一系列生长因子来促进 WIHN。