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一种新的鳞状细胞分化标志物的鉴定及其被维甲酸抑制的情况。

Identification of a new squamous cell differentiation marker and its suppression by retinoids.

作者信息

Lotan R, Pieniazek J, George M D, Jetten A M

机构信息

Department of Tumor Biology, University of Texas M. D. Anderson Cancer Center, Houston 77030.

出版信息

J Cell Physiol. 1992 Apr;151(1):94-102. doi: 10.1002/jcp.1041510114.

Abstract

Rabbit tracheobronchial epithelial cells (RbTE) can undergo squamous cell differentiation under defined culture conditions and, therefore, have been used as a model to study the regulation of squamous cell differentiation markers. In the present study, we identified a 20-kDa protein, designated rSQ20, in the serum-free growth medium conditioned by RbTE cells undergoing squamous cell differentiation. The protein was also found in extracts of squamous differentiated cells. rSQ20 was labeled by cells incubated with [35S]methionine but not with [3H]glucosamine, suggesting that it is not a glycoprotein. Undifferentiated cells did not produce this protein. rSQ20 was detected in the conditioned medium of RbTE cells after they reached a confluent and growth-arrested state, and thereafter its level increased markedly and concurrently with an increase in type I (epidermal) transglutaminase, an established marker of squamous cell differentiation. rSQ20 found in concentrated conditioned medium of squamous differentiated RbTE cells was eluted from a gel filtration column as a protein of 20 kDa, similar to that found by gel electrophoresis under denaturing conditions, suggesting that it is not a multimeric protein. A protein with an apparent molecular weight of 16 kDa (rSQ16), probably the product of partial proteolysis of rSQ20, was often found in various amounts in the conditioned medium of differentiated RbTE cells. beta-All-trans retinoic acid and other vitamin A analogues (retinoids), which suppress squamous cell differentiation, inhibited the expression of rSQ20 in RbTE cells. RbTE cells immortalized by transfection with SV40 large T antigen as well as malignantly transformed derivatives obtained from the immortalized cells by further transfection with v-Ha-ras secreted SQ20 and SQ16 when grown to high cell densities although their squamous differentiation was impaired. An analogous protein with an apparent molecular weight of 16 kDa, designated hSQ16, was detected in the medium of differentiated normal human bronchial epithelial (NHBE) cells and normal human epidermal keratinocytes (NHEK). No such protein could be detected in the medium in which undifferentiated NHBE or NHEK cells were grown. These results suggest that rSQ20 and hSQ16 are new markers of squamous cell differentiation.

摘要

兔气管支气管上皮细胞(RbTE)在特定培养条件下可发生鳞状细胞分化,因此已被用作研究鳞状细胞分化标志物调控的模型。在本研究中,我们在经历鳞状细胞分化的RbTE细胞条件无血清生长培养基中鉴定出一种20 kDa的蛋白质,命名为rSQ20。在鳞状分化细胞提取物中也发现了该蛋白质。rSQ20可被用[35S]甲硫氨酸孵育的细胞标记,但不能被[3H]葡糖胺标记,这表明它不是糖蛋白。未分化细胞不产生这种蛋白质。RbTE细胞达到汇合和生长停滞状态后,在其条件培养基中检测到rSQ20,此后其水平显著增加,同时I型(表皮)转谷氨酰胺酶增加,这是一种已确定的鳞状细胞分化标志物。在鳞状分化的RbTE细胞浓缩条件培养基中发现的rSQ20从凝胶过滤柱上洗脱下来时为20 kDa的蛋白质,类似于在变性条件下通过凝胶电泳发现的蛋白质,这表明它不是多聚体蛋白。在分化的RbTE细胞条件培养基中经常发现一种表观分子量为16 kDa的蛋白质(rSQ16),它可能是rSQ20部分蛋白水解的产物。抑制鳞状细胞分化的β-全反式维甲酸和其他维生素A类似物(类视黄醇)抑制RbTE细胞中rSQ20的表达。用SV40大T抗原转染永生化的RbTE细胞以及通过进一步用v-Ha-ras转染从永生化细胞获得的恶性转化衍生物,当生长到高细胞密度时会分泌SQ20和SQ16,尽管它们的鳞状分化受损。在分化的正常人支气管上皮(NHBE)细胞和正常人表皮角质形成细胞(NHEK)培养基中检测到一种表观分子量为16 kDa的类似蛋白质,命名为hSQ16。在未分化的NHBE或NHEK细胞生长的培养基中未检测到这种蛋白质。这些结果表明rSQ20和hSQ16是鳞状细胞分化的新标志物。

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