畜牧兽医学报 ›› 2024, Vol. 55 ›› Issue (2): 515-527.doi: 10.11843/j.issn.0366-6964.2024.02.010

• 遗传育种 • 上一篇    下一篇

半胱氨酸、蛋氨酸对体外培养绒山羊次级毛囊生长及毛乳头细胞增殖的影响

康佳, 段香茹, 尹雪姣, 杨若晨, 李太春, 单新雨, 陈美静, 张英杰*, 刘月琴*   

  1. 河北农业大学动物科技学院, 保定 071000
  • 收稿日期:2023-07-25 出版日期:2024-02-23 发布日期:2024-02-27
  • 通讯作者: 张英杰,主要从事羊的繁殖调控与反刍动物营养研究,E-mail:zhangyingjie66@126.com;刘月琴,主要从事羊的繁殖调控与反刍动物营养研究,E-mail:Liuyueqin66@126.com
  • 作者简介:康佳(1999-),男,满族,河北秦皇岛人,硕士生,主要从事动物营养与饲料科学的研究,E-mail:2504715156@qq.com
  • 基金资助:
    国家绒毛用羊产业体系项目(CARS-39)

Effects of Cysteine and Methionine on Secondary Hair Follicle Growth and Hair Dermal Papilla Cell Proliferation in vitro in Cashmere Goats

KANG Jia, DUAN Xiangru, YIN Xuejiao, YANG Ruochen, LI Taichun, SHAN Xinyu, CHEN Meijing, ZHANG Yingjie*, LIU Yueqin*   

  1. College of Animal Science and Technology, Hebei Agricultural University, Baoding 071000, China
  • Received:2023-07-25 Online:2024-02-23 Published:2024-02-27

摘要: 旨在探讨半胱氨酸(Cys)、蛋氨酸(Met)对体外培养燕山绒山羊次级毛囊(SF)生长及毛乳头细胞(DPCs)增殖凋亡的影响。本研究选取1只1周岁左右健康雄性燕山绒山羊皮肤若干,完整分离的次级毛囊随机分成Cys试验组和Met试验组,每组各浓度3个重复,每个重复8根毛囊,Cys试验组添加浓度分别为0、40、80、120、160和200 μg·mL-1;Met试验组添加浓度分别为0、10、15、20、25和30 μg·mL-1。毛囊培养7 d,每隔24 h观察毛囊生长形态并测量毛囊生长长度。从燕山绒山羊次级毛囊中提取、纯化DPCs,细胞计数并绘制DPCs生长曲线,将DPCs随机分为Cys试验组和Met试验组,每组各浓度6个重复,Cys试验组添加浓度分别为0、20、40、60、80、100 μg·mL-1;Met试验组添加浓度分别为0、2、4、6、8、10 μg·mL-1。培养2 h后用CCK-8试剂盒进行细胞增殖活力测定,确定燕山绒山羊DPCs中Cys和Met的最适培养浓度,利用qRT-PCR技术检测不同浓度Cys和Met的DPCs增殖相关基因(PCNACCND1、CDC42、CDK4)、凋亡相关基因(P21、P53、BaxCaspase-3、Bcl-2)、皮肤细胞分化相关基因(IVL)及角蛋白相关基因(K10、K14)mRNA表达水平。结果表明,与对照组相比,添加80和120 μg·mL-1 Cys与10、15、20和25 μg·mL-1 Met均可显著影响次级毛囊生长速率和累计生长长度(P<0.01),且120 μg·mL-1 Cys和20 μg·mL-1 Met促生长效果最好;添加20、40和60 μg·mL-1 Cys可以显著影响DPCs增殖(P<0.05),添加40 μg·mL-1Cys显著上调PCNACCND1、CDK4、Bcl-2、K10、K14和IVL基因mRNA表达量(P<0.05);添加6 μg·mL-1 Met可以显著影响DPCs增殖(P<0.05),并显著上调PCNACCND1、CDK4、P21、Bcl-2、K10和K14基因mRNA表达量(P<0.05)。综上,添加Cys和Met可以显著促进长绒期燕山绒山羊次级毛囊生长,最适添加量分别为120 μg·mL-1和20 μg·mL-1;添加Cys和Met可通过上调细胞增殖、分化、角蛋白等基因mRNA、下调细胞凋亡基因mRNA表达,促进乳头细胞增殖、抑制细胞凋亡进而促进燕山绒山羊次级毛囊生长。

关键词: 半胱氨酸, 蛋氨酸, 绒山羊, 次级毛囊, 毛乳头细胞, 基因表达

Abstract: The aim of this study was to investigate the effects of cysteine (Cys) and methionine (Met) on the growth of secondary hair follicles (SF), and the proliferation and apoptosis of hair dermal papilla cells (DPCs) cultured in vitro of Yanshan cashmere goats. The skins of one healthy male Yanshan cashmere goat at one year old was collected, and the completely isolated secondary hair follicles were randomly divided into the Cys experimental group and the Met experimental group, with 3 replicates for each concentration in each group and 8 hair follicles for each replicate. The concentrations of the Cys experimental group were 0, 40, 80, 120, 160, and 200 μg·mL-1, respectively; the concentrations of the Met experimental group were 0, 10, 15, 20, 25, and 30 μg·mL-1, respectively. Hair follicles were cultured for 7 days, the hair follicle growth pattern was observed and hair follicle length was measured every 24 h. DPCs were extracted and purified from the secondary hair follicles of Yanshan cashmere goats, the cells were counted, and the growth curves of DPCs were plotted. The DPCs were randomly divided into the Cys experimental group and the Met experimental group, with 6 replicates of each concentration in each group. The concentrations of the Cys experimental group were 0, 20, 40, 60, 80, and 100 μg·mL-1, respectively; and the concentrations of the Met experimental group were 0, 2, 4, 6, 8, and 10 μg·mL-1, respectively. After 2 h of incubation, cell proliferation viability was detected using the CCK-8 kit to determine the optimal culture concentration of Cys and Met in Yanshan cashmere goat DPCs. The qRT-PCR was used to detect the mRNA expression levels of proliferation-related genes (PCNA, CCND1, CDC42, CDK4), apoptosis-related genes (P21, P53, Bax, Caspase-3, Bcl-2), skin cell differentiation-related gene (IVL) and keratin-related genes (K10, K14) in the DPCs incubated with different concentrations of Cys and Met. Compared with the control group, the addition of 80 and 120 μg·mL-1 Cys and 10, 15, 20, and 25 μg·mL-1 Met significantly affected the growth rate and cumulative growth length of secondary hair follicles (P<0.01), and the growth-promoting effects of 120 μg·mL-1 Cys and 20 μg·mL-1 Met groups were the best. The addition of 20, 40, and 60 μg·mL-1 Cys significantly affected the proliferation of DPCs (P<0.05), and the addition of 40 μg·mL-1 Cys significantly up-regulated the expressions of PCNA, CCND1 and CDK4, Bcl-2, K10, K14, and IVL genes mRNA (P<0.05); the addition of 6 μg·mL-1 Met could significantly affect the proliferation of DPCs and significantly up-regulate the expressions of PCNA, CCND1, CDK4, P21, Bcl-2, K10, and K14 genes mRNA (P<0.05). In conclusion, the addition of Cys and Met could significantly promote the growth of secondary hair follicles in Yanshan cashmere goats during the growing-fleece period, and the optimal addition concentrations were 120 μg·mL-1 and 20 μg·mL-1, respectively. The addition of Cys and Met could promote the proliferation of hair dermal papilla cells and inhibit apoptosis through upregulating the expression of genes for cell proliferation, differentiation, keratin, and other genes, and downregulating the expression of mRNA of apoptotic genes, which could promote the growth of secondary hair follicles of Yanshan cashmere goats.

Key words: cysteine, methionine, cashmere goats, secondary hair follicles, hair dermal papilla cells, gene expression

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