中华皮肤科杂志 ›› 2020, Vol. 53 ›› Issue (12): 967-973.doi: 10.35541/cjd.20190495

• 论著 • 上一篇    下一篇

Klhl24基因起始密码子突变小鼠毛囊异常生理表型分析

赵倩1    宋忠亚1    杨勇1,2   

  1. 1北京大学第一医院皮肤科  北京市皮肤病分子诊断重点实验室  国家皮肤与免疫疾病临床医学研究中心  100034;2中国医学科学院  北京协和医学院  皮肤病医院遗传中心,南京  210042
  • 收稿日期:2019-04-15 修回日期:2020-09-15 发布日期:2020-12-02
  • 通讯作者: 杨勇 E-mail:yyang@pumcderm.cams.cn
  • 基金资助:
    国家自然科学基金(81730084);中国博士后科学基金(2017M620543)

Analysis of abnormal physiological phenotype of hair follicles in mice carrying the Klhl24 gene initiation codon mutation

Zhao Qian1, Song Zhongya1, Yang Yong1,2   

  1. 1Department of Dermatology, Peking University First Hospital, Beijing Key Laboratory of Molecular Diagnosis on Dermatoses, National Clinical Research Center for Skin and Immune Diseases, Beijing 100034, China; 2Genetic Skin Disease Center, Hospital for Skin Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing 210042, China
  • Received:2019-04-15 Revised:2020-09-15 Published:2020-12-02
  • Contact: Yang Yong E-mail:yyang@pumcderm.cams.cn
  • Supported by:
    National Natural Science Foundation of China (81730084); China Postdoctoral Science Foundation (2017M620543)

摘要: 【摘要】 目的 探究Klhl24基因起始密码子突变小鼠毛囊异常的生理表型,为阐明Klhl24调控毛囊发育的机制提供基础。方法 将通过CRISPER/Cas9技术构建的Klhl24基因起始密码子突变Klhl24c.3G>T杂合(Klhl24c.3G/T)雄性小鼠与野生型雌性小鼠杂交,对同窝小鼠进行基因型鉴定, Klhl24c.3G/T雄性小鼠和野生型(WT)雄性小鼠分别作为实验组与对照组,每组小鼠 ≥ 3只。在小鼠出生后第21天(第1个毛发静止期)及45天(第2个毛发静止期)进行胶带贴毛实验,对小鼠背部皮肤组织进行Ki67免疫组化检测,并用扫描电镜、透射电镜观察,用脱氧核糖核苷酸介导的dUTP末端标记(TUNEL)试剂盒检测毛囊内凋亡细胞。实验组与对照组检测结果比较采用Dunnett-t检验。结果 第1个静止期与第2个静止期Klhl24c.3G/T小鼠每0.25 cm2胶带脱落毛干数量分别为1 224 ± 51.08与1 514 ± 72.15,WT小鼠分别为320 ± 55.68和125 ± 2.86,第1、2个静止期Klhl24c.3G/T小鼠脱落毛干数量均明显多于WT小鼠(t = 11.96、19.24,均P < 0.001)。对第1个静止期脱落毛干进行扫描电镜观测,显示脱落毛干底部呈杵状。出生后第59天时,WT小鼠背部无新毛干长出,毛囊处于静止期,而Klhl24c.3G/T小鼠背部已有新毛干长出,毛囊进入下一个生长期。透射电镜观察显示,在第1个毛囊静止期(P21)Klhl24c.3G/T小鼠背部皮肤毛囊细胞中线粒体内嵴结构混乱,单个毛囊结构中凋亡细胞数量为12 ± 1.15,高于WT小鼠(3 ± 0.63,n = 8,t = 6.874,P < 0.001)。结论 Klhl24c.3G/T小鼠毛发异常表型主要为毛囊静止期锚定毛干能力降低,毛囊生长期提前,毛囊细胞中线粒体结构异常,并且凋亡细胞数量增加。

关键词: 毛囊, 小鼠, 突变型, 秃发, 线粒体, 细胞凋亡, Klhl24基因

Abstract: 【Abstract】 Objective To investigate the abnormal physiological phenotype of hair follicles in mice with the Klhl24 gene initiation codon mutation, and to provide a basis for elucidating the regulatory mechanism of hair follicle development by the gene. Methods A Klhl24c.3G/T male mouse carrying a heterozygous mutation Klhl24c.3G>T in the initiation codon of the Klhl24 gene was produced by using clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technology, and mated with 2 wild-type female mice. Then, the littermate mice were genotyped. The Klhl24c.3G/T male mice and wild-type male mice served as the experimental group and control group respectively, and there were more than 3 mice in each group. On days 21 (the first telogen phase of hair cycle) and 45 (the second telogen phase of hair cycle) after birth, the tape sticking experiment was carried out. Immunohistochemical study of Ki67 expression was performed in skin tissues from the back of the mice, scanning electron microscopy and transmission electron microscopy were conducted to observe the hair root at the bottom of the hair shaft and the structure of mitochondria in skin tissues respectively, and a terminal deoxyribonucleotide transferase-mediated dUTP nick end labeling (TUNEL) kit was used to detect apoptosis in hair follicles. The Dunnett-t test was used for comparisons between the experimental group and control group. Results The number of shed hair shafts per 0.25 cm2 of the tape at the first and second telogen phases was significantly higher in the Klhl24c.3G/T mice (1 224 ± 51.08, 1 514 ± 72.15 respectively) than in the wild-type mice (320 ± 55.68, 125 ± 2.86, t = 11.96, 19.24, respectively, both P < 0.001). Scanning electron microscopy showed clubbed hair roots at the bottom of the shed hair shaft at the first telogen phase. On day 59 after birth, there was no new hair shaft growing on the back of the wild-type mice and the hair follicles were still at the telogen phase, while new hair shafts had grown on the back of the Klhl24c.3G/T mice and the hair follicles had entered the next anagen phase. At the first telogen phase (i.e., on day 21), transmission electron microscopy showed disordered structures of mitochondrial cristae in cells of the hair follicles in the skin tissues from the back of the Klhl24c.3G/T mice, and the number of apoptotic cells in hair follicles (12 ± 1.15) was significantly higher in the Klhl24c.3G/T mice than in the wild-type mice (3 ± 0.63, n = 8, t = 6.874, P < 0.001). Conclusion The abnormal hair phenotype of the Klhl24c.3G/T mice mainly manifested as decreased anchoring ability of hair shafts at the telogen phase, precocious entry into the anagen phase, abnormal structure of mitochondria in hair follicle cells, and increased number of apoptotic cells.

Key words: Hair follicle, Mice, mutant strains, Alopecia, Mitochondria, Apoptosis, Klhl24 gene

引用本文

赵倩 宋忠亚 杨勇, . Klhl24基因起始密码子突变小鼠毛囊异常生理表型分析[J]. 中华皮肤科杂志, 2020,53(12):967-973. doi:10.35541/cjd.20190495

Zhao Qian, Song Zhongya, Yang Yong, . Analysis of abnormal physiological phenotype of hair follicles in mice carrying the Klhl24 gene initiation codon mutation[J]. Chinese Journal of Dermatology, 2020, 53(12): 967-973.doi:10.35541/cjd.20190495