首页> 外文期刊>Asian-Australasian Journal of Animal Sciences >Validation of Methods for Isolation and Culture of Alpaca Melanocytes: A Novel Tool for In vitro Studies of Mechanisms Controlling Coat Color
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Validation of Methods for Isolation and Culture of Alpaca Melanocytes: A Novel Tool for In vitro Studies of Mechanisms Controlling Coat Color

机译:羊驼黑素细胞的分离和培养方法的验证:一种用于控制毛色机制的体外研究的新工具

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摘要

The objective of the present studies was to develop and validate a system for isolation, purification and extended culture of pigment-producing cells in alpaca skin (melanocytes) responsible for coat color and to determine the effect of alpha melanocyte stimulating hormone treatment on mRNA expression for the melanocortin I receptor, a key gene involved in coat color regulation in other species. Skin punch biopsies were harvested from the dorsal region of 1-3 yr old alpacas and three different enzyme digestion methods were evaluated for effects on yield of viable cells and attachment in vitro. Greatest cell yields and attachment were obtained following dispersion with dispase II relative to trypsin and trypsin-EDTA treatment. Culture of cells in medium supplemented with basic fibroblast growth factor, bovine pituitary extract, hydrocortisone, insulin, 12-O-tetradecanolphorbol-13-acetate and cholera toxin yielded highly pure populations of melanocytes by passage 3 as confirmed by detection of tyrosinase activity and immunocytochemical localization of melanocyte markers including tyrosinase, S-100 and micropthalmia-associated transcription factor. Abundance of mRNA for tyrosinase, a key enzyme in melanocyte pigment production, was maintained through 10 passages showing preservation of melanocyte phenotypic characteristics with extended culture. To determine hormonal responsiveness of cultured melanocytes and investigate regulation of melanocortin I receptor expression, cultured melanocytes were treated with increasing concentrations of alpha-melanocyte stimulating hormone. Treatment with alpha-melanocyte stimulating hormone increased melanocortin receptor I mRNA in a dose dependent fashion. The results demonstrated culture of pure populations of alpaca melanocytes to 10 passages and illustrate the potential utility of such cells for studies of intrinsic and extrinsic regulation of genes controlling pigmentation and coat color in fiber-producing species.
机译:本研究的目的是开发和验证一种系统,用于隔离,纯化和扩展负责羊驼毛颜色的羊驼皮肤(黑色素细胞)中色素生成细胞的培养,并确定α黑色素刺激激素治疗对mRNA表达的影响。 melanocortin I受体,一种与其他物种的毛色调节有关的关键基因。从1-3岁的羊驼背侧区域进行皮肤穿孔活检,并评估三种不同的酶消化方法对活细胞产量和体外附着的影响。相对于胰蛋白酶和胰蛋白酶-EDTA处理,用分散酶II分散后可获得最大的细胞产量和附着力。通过酪氨酸酶活性和免疫细胞化学检测证实,在补充了碱性成纤维细胞生长因子,牛垂体提取物,氢化可的松,胰岛素,12-O-十四醇佛波醇-13-乙酸盐和霍乱毒素的培养基中培养细胞可产生高纯度的黑色素细胞群。黑色素细胞标志物的定位,包括酪氨酸酶,S-100和与小肺炎相关的转录因子。酪氨酸酶是黑素细胞色素生成中的关键酶,其mRNA的丰度可通过10次传代得以维持,这表明通过扩展培养可保持黑素细胞表型特征。为了确定培养的黑素细胞的激素反应性并研究黑皮质素I受体表达的调节,用增加浓度的α-黑素细胞刺激激素处理培养的黑素细胞。用α-黑素细胞刺激激素治疗以剂量依赖性方式增加了黑皮质素受体I mRNA。结果证明了羊驼黑素细胞的纯种群培养到10代,并说明了这种细胞在研究内在和外在调节控制纤维生产物种中色素沉着和皮毛颜色的基因的潜在用途。

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