Suo Liye, VanBuren Christine, Hovland Eylul Damla, Kedishvili Natalia Y, Sundberg John P, Everts Helen B
Department of Human Nutrition, The Ohio State University, Columbus, OH, United States.
Department of Nutrition and Food Sciences, Texas Woman's University, Denton, TX, United States.
Front Cell Dev Biol. 2021 Feb 5;9:571474. doi: 10.3389/fcell.2021.571474. eCollection 2021.
Hair follicles cycle through periods of growth (anagen), regression (catagen), rest (telogen), and release (exogen). Telogen is further divided into refractory and competent telogen based on expression of bone morphogenetic protein 4 (BMP4) and wingless-related MMTV integration site 7A (WNT7A). During refractory telogen hair follicle stem cells (HFSC) are inhibited. Retinoic acid synthesis proteins localized to the hair follicle and this localization pattern changed throughout the hair cycle. In addition, excess retinyl esters arrested hair follicles in telogen. The purpose of this study was to further define these hair cycle changes. BMP4 and WNT7A expression was also used to distinguish refractory from competent telogen in C57BL/6J mice fed different levels of retinyl esters from two previous studies. These two studies produced opposite results; and differed in the amount of retinyl esters the dams consumed and the age of the mice when the different diet began. There were a greater percentage of hair follicles in refractory telogen both when mice were bred on an unpurified diet containing copious levels of retinyl esters (study 1) and consumed excess levels of retinyl esters starting at 12 weeks of age, as well as when mice were bred on a purified diet containing adequate levels of retinyl esters (study 2) and remained on this diet at 6 weeks of age. WNT7A expression was consistent with these results. Next, the localization of vitamin A metabolism proteins in the two stages of telogen was examined. Keratin 6 (KRT6) and cellular retinoic acid binding protein 2 (CRABP2) localized almost exclusively to refractory telogen hair follicles in study 1. However, KRT6 and CRABP2 localized to both competent and refractory telogen hair follicles in mice fed adequate and high levels of retinyl esters in study 2. In mice bred and fed an unpurified diet retinol dehydrogenase SDR16C5, retinal dehydrogenase 2 (ALDH1A2), and cytochrome p450 26B1 (CYP26B1), enzymes and proteins involved in RA metabolism, localized to BMP4 positive refractory telogen hair follicles. This suggests that vitamin A may contribute to the inhibition of HFSC during refractory telogen in a dose dependent manner.
毛囊经历生长(生长期)、退化(退行期)、休止(休止期)和脱落(脱落期)的循环。根据骨形态发生蛋白4(BMP4)和无翅相关MMTV整合位点7A(WNT7A)的表达,休止期进一步分为难治性休止期和活性休止期。在难治性休止期,毛囊干细胞(HFSC)受到抑制。视黄酸合成蛋白定位于毛囊,且这种定位模式在整个毛发周期中发生变化。此外,过量的视黄酯会使毛囊停滞在休止期。本研究的目的是进一步明确这些毛发周期变化。在两项先前的研究中,还利用BMP4和WNT7A的表达来区分C57BL/6J小鼠中难治性休止期和活性休止期,这些小鼠摄入了不同水平的视黄酯。这两项研究得出了相反的结果;在母鼠摄入视黄酯的量以及开始不同饮食时小鼠的年龄方面存在差异。当小鼠在含有大量视黄酯的未纯化饮食中繁殖(研究1)且从12周龄开始摄入过量视黄酯时,以及当小鼠在含有适量视黄酯的纯化饮食中繁殖(研究2)且在6周龄时继续食用这种饮食时,处于难治性休止期的毛囊百分比更高。WNT7A的表达与这些结果一致。接下来,研究了视黄酸代谢蛋白在休止期两个阶段的定位。在研究1中,角蛋白6(KRT6)和细胞视黄酸结合蛋白2(CRABP2)几乎只定位于难治性休止期毛囊。然而,在研究2中,摄入适量和高水平视黄酯的小鼠中,KRT6和CRABP2定位于活性休止期和难治性休止期毛囊。在繁殖并喂食未纯化饮食的小鼠中,视黄醇脱氢酶SDR16C5、视网膜脱氢酶2(ALDH1A2)和细胞色素p450 26B1(CYP26B1),这些参与视黄酸代谢的酶和蛋白,定位于BMP4阳性的难治性休止期毛囊。这表明视黄酸可能以剂量依赖的方式在难治性休止期对毛囊干细胞的抑制起作用。