在化学定义的无动物源性细胞培养物中重建人体表皮的特征

Julia Bajsert , Valérie De Glas , Emilie Faway , Catherine Lambert de Rouvroit , Miguel Pérez-Aso , Paul W. Cook , Yves Poumay
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引用次数: 0

摘要

源自表皮角质细胞的重建人体表皮(RHE)模型为动物实验提供了一种符合伦理和科学的替代方法,特别是在皮肤毒理学和皮肤病学研究中,消除对动物的残忍行为至关重要。因此,我们比较了市面上专为再生医学设计的不含动物源化学成分(cdAOF)的补充剂和广泛使用的补充剂(人类角质细胞生长补充剂),后者含有生长因子和牛垂体提取物。在此,我们介绍了在 cdAOF 条件下从新生、成年和永生 N/端粒酶逆转录酶角质形成细胞中提取的 RHE 的扩展特征。在 cdAOF 培养基中培养 RHE 所产生的组织学特征与使用人类角质形成细胞生长补充剂所产生的组织学特征相似,但基底角质形成细胞不是圆柱形。此外,在 cdAOF 条件下,基底层内含蛋白的免疫定位和几种炎症-增殖标志物的 mRNA 表达都有所增加。在 cdAOF 培养基中培养的 RHE 中,其他预期的角质化标志物的表达和免疫定位相似,而对屏障功能(跨上皮电阻)的监测结果显示,在统计学上与在人类角质形成细胞生长补充剂中培养的 RHE 中观察到的结果相同或更低。我们的研究表明,在 cdAOF 培养条件下可以完成 RHE 的重建,进一步的改进可以促进其在再生医学以外的体外毒理学应用中的扩大使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of Reconstructed Human Epidermis in a Chemically-Defined, Animal Origin-Free Cell Culture

The Reconstructed Human Epidermis (RHE) model derived from epidermal keratinocytes offers an ethical and scientific alternative to animal experimentation, particularly in cutaneous toxicology and dermatological research, where the elimination of animal cruelty is of paramount importance. Thus, we compared commercially available chemically defined animal origin-free (cdAOF) supplements, designed for regenerative medicine, to the widely utilized supplement (human keratinocyte growth supplement), which contains growth factors and bovine pituitary extract. Herein we present the extended characterization of RHE derived from newborn, adult, and immortalized N/telomerase reverse transcriptase keratinocytes under cdAOF conditions. Culture of RHE in the cdAOF media produced histological features that were similar to that produced using human keratinocyte growth supplement, with the exception that the basal keratinocytes were less cylindrical. Additionally, immunolocalization of involucrin in the basal layer and increased mRNA expression of several inflammatory-proliferative markers were observed under cdAOF conditions. In RHEs cultured in cdAOF media, expression and immunolocalization of other expected markers of keratinization were similar, while monitoring of barrier function (transepithelial electrical resistance) revealed results that were statistically equal to, or lower than those observed in RHE cultured in human keratinocyte growth supplement. Our study indicates that reconstruction of RHE was accomplished under cdAOF culture conditions and that further refinement could promote an expanded use beyond regenerative medicine, for in vitro toxicology applications.

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