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人类毛囊角蛋白:“过度增殖性”角蛋白在体内和体外的外根鞘细胞中持续表达。

Keratins of the human hair follicle: "hyperproliferative" keratins consistently expressed in outer root sheath cells in vivo and in vitro.

作者信息

Stark H J, Breitkreutz D, Limat A, Bowden P, Fusenig N E

机构信息

Institute of Biochemistry, German Cancer Research Center, Heidelberg.

出版信息

Differentiation. 1987;35(3):236-48. doi: 10.1111/j.1432-0436.1987.tb00174.x.

Abstract

Keratins produced by morphologically distinct compartments of the human hair folicle (hHF) were analysed and compared to those produced by cultured hHF and interfollicular keratinocytes. Five of the major keratins, the basic keratins nos. 5 and 6 (apparent mol. mass 60 and 58 kDa) and the acidic keratins nos. 14, 16, and 17 (51, 49 and 48 kDa), could be labelled in intact hHF and were found in all fractions of the outer root sheath (ORS). The other major keratins, which were not labelled under these conditions (basic-neutral hHbI and -II; 60-62 kDa and acidic hHaI and -II; 40-42 kDa) were associated with hair shaft (hHS) both in the follicle and, virtually unchanged, in the distal part of the hair. Another, previously undescribed, group of proteins with keratin-like properties exhibiting a broad pI-spectrum (basic to slightly acidic: hIC-I, -II, -III, 64-67 kDa; distinctly acidic: hIC-IV, about 54 kDa) was detected in isolated inner root sheath (IRS), in the cuticular material shed from denuded hHS, and also in nail plates. In our experiments only ORS cells grew readily in culture irrespective of their origin from peripheral (mesenchyme-adjacent) or more central ORS-cell layers. In contrast to keratinocytes from interfollicular epidermis (IFE) the cultured ORS cells expressed a keratin set virtually identical to that expressed in vivo. This set also closely resembled that expressed by IFE keratinocyte cultures. The identity of the respective keratins (nos. 5, 6, 14, 16, and 17) present in all these cells in vivo and in vitro was confirmed by tryptic peptide mapping. The data indicated that the microenvironment (in situ) directs the differentiation of ORS cells in a manner comparable to the way it is directed by conventional culture conditions, with consistent expression of the "basal" and "hyperproliferative" set of keratins. This, however, does not exclude the possibility that other types of environmentally induced response may occur, as seen for example during the reepithelialization of superficial skin wounds by ORS cells.

摘要

对人毛囊(hHF)形态学上不同区域产生的角蛋白进行了分析,并与培养的hHF和毛囊间角质形成细胞产生的角蛋白进行了比较。五种主要角蛋白,即碱性角蛋白5号和6号(表观分子量分别为60 kDa和58 kDa)以及酸性角蛋白14号、16号和17号(51 kDa、49 kDa和48 kDa),可在完整的hHF中标记,并在外根鞘(ORS)的所有部分中发现。在这些条件下未被标记的其他主要角蛋白(碱性-中性hHbI和-II;60 - 62 kDa以及酸性hHaI和-II;40 - 42 kDa)在毛囊中的毛干(hHS)以及毛发远端基本未变的部分中均有存在。在分离的内根鞘(IRS)、从裸露的hHS脱落的角质层物质以及指甲板中检测到另一组先前未描述的具有角蛋白样特性的蛋白质,其表现出较宽的pI谱(从碱性到微酸性:hIC-I、-II、-III,64 - 67 kDa;明显酸性:hIC-IV,约54 kDa)。在我们的实验中,无论ORS细胞起源于外周(间充质相邻)还是更中央的ORS细胞层,只有ORS细胞能在培养中容易生长。与毛囊间表皮(IFE)的角质形成细胞相反,培养的ORS细胞表达的角蛋白组与体内表达的几乎相同。该角蛋白组也与IFE角质形成细胞培养物表达的角蛋白组非常相似。通过胰蛋白酶肽图谱分析证实了体内和体外所有这些细胞中存在的相应角蛋白(5号、6号、14号、16号和17号)的一致性。数据表明,微环境(原位)以类似于传统培养条件指导的方式指导ORS细胞的分化,角蛋白的“基础”和“过度增殖”组有一致的表达。然而,这并不排除可能发生其他类型的环境诱导反应的可能性,例如在ORS细胞对浅表皮肤伤口进行再上皮化过程中所见。

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