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从表皮和口腔黏膜培养的人角质形成细胞中与增殖和分化相关标志物的基因表达。

Gene expression of markers associated with proliferation and differentiation in human keratinocytes cultured from epidermis and from buccal mucosa.

作者信息

Brysk M M, Arany I, Brysk H, Chen S H, Calhoun K H, Tyring S K

机构信息

Department of Dermatology, University of Texas Medical Branch, Galveston 77555, USA.

出版信息

Arch Oral Biol. 1995 Sep;40(9):855-62. doi: 10.1016/0003-9969(95)00046-r.

Abstract

Normal keratinocytes from epidermis and from buccal mucosa underwent dissimilar stages of differentiation in the same culture medium and responded differently to changes in the composition of the medium. Manifestations of these variations were examined in terms of the expression at the mRNA level (as measured by reverse transcriptase-polymerase chain reaction) of three regulatory genes (cdc2, c-myc, and p53) and five that encode structural proteins (keratins K5, K10 and K13, involucrin, and filaggrin), in three growth-medium formulations. The culture conditions enhanced or retarded maturation; the observed alterations in gene expression correlated with these changes. Except for the proliferation genes, the non-keratinizing buccal mucosa generally responded more weakly than the orthokeratotic epidermis to culture-medium supplementation favouring differentiation. Gene expression in cultured keratinocytes reflected their ability to differentiate in vivo; genes were expressed even when the corresponding protein was not seen in vitro. Although keratin K10 is not prevalent in the buccal mucosa nor keratin K13 in the epidermis, the genes for both were found to be expressed in both tissues.

摘要

来自表皮和颊黏膜的正常角质形成细胞在同一培养基中经历了不同的分化阶段,并且对培养基成分的变化反应不同。在三种生长培养基配方中,根据三个调节基因(cdc2、c-myc和p53)以及五个编码结构蛋白的基因(角蛋白K5、K10和K13、兜甲蛋白和丝聚蛋白)在mRNA水平的表达(通过逆转录聚合酶链反应测量)来研究这些差异的表现。培养条件促进或延缓了成熟;观察到的基因表达变化与这些变化相关。除了增殖基因外,非角化的颊黏膜通常比正角化的表皮对有利于分化的培养基补充反应更弱。培养的角质形成细胞中的基因表达反映了它们在体内的分化能力;即使在体外未观察到相应蛋白质时,基因也会表达。尽管角蛋白K10在颊黏膜中不普遍,角蛋白K13在表皮中不普遍,但发现这两种基因在两种组织中均有表达。

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