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用于生产可移植表皮片的小鼠角质形成细胞培养的优化。

Optimization of murine keratinocyte culture for the production of graftable epidermal sheets.

作者信息

Rouabhia M, Germain L, Bélanger F, Guignard R, Auger F A

机构信息

Laboratoire de Recherche des Grands Brûlés, Hôpital du Saint-Sacrement, Québec, Canada.

出版信息

J Dermatol. 1992 Jun;19(6):325-34. doi: 10.1111/j.1346-8138.1992.tb03234.x.

Abstract

The aim of the present study was to optimize murine epidermal cell cultures in order to obtain graftable sheets. Newborn (1-3 days old) Balb/c mice skin were used to optimize culture media and plating cell concentration, then epidermal sheet production, and grafting. Epidermal cells were plated at various concentrations in different culture media containing low (0.1 mM) or high (greater than 1 mM) Ca2+ levels. After a 3 day culture at the 10(4) cells/cm2 plating cell concentration, the percentage of differentiated cells was more than 80% in the high Ca2+ culture medium and less than 50% with bulky cells in the low Ca2+ culture medium. Under these conditions confluence was not obtained. At the 10(5) cells/cm2 seeding inoculum, the percentage of confluence increased to 95-100% during the first 72 h of culture in both high and low Ca2+ culture media. Three-day-old culture showed stratified multilayer epidermal sheets in the high calcium medium, and monolayer epidermal sheets were present in the low calcium medium after seeding keratinocytes in fibronectin precoated flasks. Seven days after plating, post confluent cultures were composed of a high percentage of differentiated cells (90%) with an increase in shedding cells in the medium. Considering the above morphological observations, sheets obtained with 10(5) cells/cm2 in MCDB-153 (A), DME-HAM (B) or GMEM (C) media after 3 days in culture were grafted. Twenty days after grafting, histological analysis of biopsies showed an epidermal structure and organization comparable to normal murine epidermis without hair follicles. Epidermal transplants showed a complete basement membrane, hemidesmosomes, and tonofilament bundles. Sheets obtained after seven day culture in all media showed lower coverage of the wound bed. These studies point out the importance of the plating cell and Ca2+ concentrations, and the culture time for murine keratinocyte confluence and differentiation to obtain graftable epidermal sheets.

摘要

本研究的目的是优化小鼠表皮细胞培养,以获得可用于移植的表皮片。使用新生(1 - 3日龄)的Balb/c小鼠皮肤来优化培养基和接种细胞浓度,进而优化表皮片的生产及移植。将表皮细胞以不同浓度接种于含有低(0.1 mM)或高(大于1 mM)钙离子水平的不同培养基中。在接种细胞浓度为10⁴个细胞/cm²的情况下培养3天后,高钙离子培养基中分化细胞的百分比超过80%,而低钙离子培养基中含有大量细胞,分化细胞的百分比低于50%。在这些条件下未达到汇合状态。在接种量为10⁵个细胞/cm²时,在高、低钙离子培养基中培养的前72小时内,汇合百分比均增加到95 - 100%。培养3天时,高钙培养基中显示出分层的多层表皮片,在纤连蛋白预包被的培养瓶中接种角质形成细胞后,低钙培养基中存在单层表皮片。接种7天后,汇合后的培养物由高比例的分化细胞(90%)组成,培养基中脱落细胞增加。考虑到上述形态学观察结果,将在MCDB - 153(A)、DME - HAM(B)或GMEM(C)培养基中培养3天后以10⁵个细胞/cm²获得的表皮片进行移植。移植20天后,活检组织的组织学分析显示,表皮结构和组织与无毛囊的正常小鼠表皮相当。表皮移植显示有完整的基底膜、半桥粒和张力丝束。在所有培养基中培养7天后获得的表皮片对创面床的覆盖较低。这些研究指出了接种细胞浓度、钙离子浓度以及培养时间对于小鼠角质形成细胞汇合和分化以获得可移植表皮片的重要性。

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