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利用细胞表面标志物CD34从毛囊隆突部富集活的小鼠角质形成细胞。

Enrichment for living murine keratinocytes from the hair follicle bulge with the cell surface marker CD34.

作者信息

Trempus Carol S, Morris Rebecca J, Bortner Carl D, Cotsarelis George, Faircloth Randall S, Reece Jeffrey M, Tennant Raymond W

机构信息

Cancer Biology Group, National Center for Toxicogenomics, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.

出版信息

J Invest Dermatol. 2003 Apr;120(4):501-11. doi: 10.1046/j.1523-1747.2003.12088.x.

Abstract

It is widely believed that epithelial stem cells reside in the hair follicle bulge region. We investigated the hematopoietic stem and progenitor cell marker, CD34, as a potential marker of hair follicle bulge keratinocytes. Using a CD34-specific antibody, we identified intense membrane staining on keratinocytes in the bulge region of the mouse hair follicle. CD34 expression colocalized with both slowly cycling (label retaining) cells and keratin 15 expression. Live CD34+ keratinocytes were positively selected using antibodies to CD34 and alpha6 integrin in combination with fluorescent activated cell sorting. Sorted cells were analyzed for DNA content, and a staining profile was generated to confirm these cells as keratinocytes. CD34+ keratinocytes were predominantly in Go/G1, in contrast to CD34- cells, which had well defined G2/M and S phases. In addition, CD34+ keratinocytes were found to express alpha6 integrin more intensely than CD34- cells (p<0.05), identifying this population as an alpha6 integrin bright subset. When seeded at clonal density, CD34+ keratinocytes formed larger colonies than CD34- cells (p<0.05), indicating a higher proliferative potential. All flow-sorted cells were positive for keratin 14 expression, and negative for keratin 1, loricrin, vimentin, and CD31. The majority of CD34+ cells (98%) were positive for keratin 6, establishing this population as basal keratinocytes of follicular origin. CD34 message was detected by reverse transcription polymerase chain reaction predominantly in the CD34+ keratinocytes, confirming specificity of the antibody. This work is the first to demonstrate that CD34 is a specific marker of bulge cell keratinocytes in the cutaneous epithelium. Furthermore, the use of this marker facilitates isolation of live epithelial cells with stem and progenitor cell characteristics, potentially providing a tool for the study of carcinogen target cells, gene therapy, and tissue engineering applications.

摘要

人们普遍认为上皮干细胞存在于毛囊隆突区。我们研究了造血干细胞和祖细胞标志物CD34,将其作为毛囊隆突角质形成细胞的潜在标志物。使用CD34特异性抗体,我们在小鼠毛囊隆突区的角质形成细胞上鉴定出强烈的膜染色。CD34表达与缓慢循环(标记保留)细胞和角蛋白15表达共定位。使用抗CD34和α6整合素抗体结合荧光激活细胞分选对活的CD34 +角质形成细胞进行阳性选择。分析分选细胞的DNA含量,并生成染色图谱以确认这些细胞为角质形成细胞。与具有明确G2 / M和S期的CD34-细胞相比,CD34 +角质形成细胞主要处于G0 / G1期。此外,发现CD34 +角质形成细胞比CD34-细胞更强烈地表达α6整合素(p <0.05),将该群体鉴定为α6整合素明亮亚群。以克隆密度接种时,CD34 +角质形成细胞形成的集落比CD34-细胞大(p <0.05),表明其增殖潜力更高。所有流式分选细胞对角蛋白14表达呈阳性,对角蛋白1、loricrin、波形蛋白和CD31呈阴性。大多数CD34 +细胞(98%)对角蛋白6呈阳性,将该群体确定为毛囊来源的基底角质形成细胞。通过逆转录聚合酶链反应主要在CD34 +角质形成细胞中检测到CD34信息,证实了抗体的特异性。这项工作首次证明CD34是皮肤上皮中隆突细胞角质形成细胞的特异性标志物。此外,使用该标志物有助于分离具有干细胞和祖细胞特征的活上皮细胞,潜在地为致癌物靶细胞研究、基因治疗和组织工程应用提供工具。

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