👤 Wenlu Jia

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273
Articles
217
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Also published as: Anna Jia, Baohui Jia, Baoyu Jia, Bin Jia, Boyin Jia, Changkai Jia, Changze Jia, Chao Jia, Chaoyue Jia, Cheng Jia, Cheng-Sheng Jia, Chi-Yu Jia, Chunhong Jia, Chunmei Jia, Da Jia, Dong-Dong Jia, Dongmei Jia, Erteng Jia, Fan Jia, Fangjuan Jia, Fangzhi Jia, Fengfeng Jia, Fuli Jia, Gong-Xue Jia, Guifang Jia, Guiyun Jia, Guobing Jia, Guoqiang Jia, Guowen Jia, Hai Jia, Hai-Yan Jia, Haibo Jia, Haiping Jia, Haiting Jia, Haiyang Jia, Haiyu Jia, Hao Jia, Haocheng Jia, Hong-Ling Jia, Hongmei Jia, Hongxiao Jia, Hongyao Jia, Hua Jia, Huaijie Jia, Huang Jia, Huanhuan Jia, Hui Jia, Huijuan Jia, Huili Jia, Huimin Jia, Huiyan Jia, Jia Jia, Jiale Jia, Jiang-Kun Jia, Jianping Jia, Jiaxin Jia, Jie Jia, Jihui Jia, Jin Jia, Jing Jia, Jingwen Jia, Jun Jia, Junjing Jia, Junling Jia, Kaiwen Jia, Kangni Jia, Ke Xin Jia, Lanbo Jia, Lei Jia, Lian-Qun Jia, Lianghui Jia, Liangliang Jia, Lianqun Jia, Lijuan Jia, Lijun Jia, Lin Jia, Lina Jia, Linna Jia, Linying Jia, Litian Jia, Liyun Jia, M C Jia, Mengshu Jia, Min Jia, Minghong Jia, Mingkun Jia, Mingyang Jia, Mingyuan Jia, Ning Jia, Ningning Jia, P Jia, Peilin Jia, Pengyu Jia, Qi Jia, Qia Jia, Qingan Jia, Qiongqiong Jia, Qiufeng Jia, Raina Y Jia, Renyong Jia, Rongjie Jia, Rongrong Jia, Ru Jia, Rui Jia, Ruimei Jia, Ruoxin Jia, Sha Jia, Shaobin Jia, Sheng Jia, Shidong Jia, Shiheng Jia, Shumin Jia, Shuying Jia, Sixiang Jia, Tao Jia, Tianzhu Jia, Tiewen Jia, Tingting Jia, W Jia, Wei Jia, Wei-Hua Jia, Weiping Jia, Weiqiang Jia, Wen-Long Jia, Wen-Wen Jia, Wen-Yan Jia, Wenfeng Jia, Wenlong Jia, Wenqian Jia, Wenshuang Jia, Wentong Jia, Wenwen Jia, Xiao Jia, Xiao-Dan Jia, Xiaodan Jia, Xiaofang Jia, Xiaohui Jia, Xiaojing Jia, Xiaomeng Jia, Xiaoming Jia, Xiaopu Jia, Xiaoqin Jia, Xiaoqing Jia, Xiaoting Jia, Xiaoyan Jia, Xilong Jia, Xin Jia, Xingyuan Jia, Xinya Jia, Xinyao Jia, Xiong Jia, Xiqun Jia, Xiyao Jia, Xu Jia, Xuan Jia, Xuebing Jia, Xueli Jia, Xueyuan Jia, Yachun Jia, Yajing Jia, Yan Jia, Yanbin Jia, Yangyang Jia, Yanhui Jia, Yanrong Jia, Yanyan Jia, Yaoyao Jia, Yaxiang Jia, Yi Jia, Yichang Jia, Yifan Jia, Yimin Jia, Ying Jia, Yizhen Jia, Yong Jia, Yongqian Jia, Youchao Jia, Yuan Jia, Yuane Jia, Yuanyuan Jia, Yucheng Jia, Yudong Jia, Yue Jia, Yuhua Jia, Yujiao Jia, Yuke Jia, Yulong Jia, Yumeng Jia, Yun Jia, Yunton Jia, Yunxiao Jia, Yutang Jia, Zhan S Jia, Zhan-Kui Jia, Zhanjun Jia, Zhankui Jia, Zhanrong Jia, Zhao Jia, Zhaojun Jia, Zhe Jia, Zhen Jia, Zhengxu Jia, Zhenhua Jia, Zhenwei Jia, Zhihao Jia, Zhimeng Jia, Zhixin Jia, Zhiying Jia, Zhumin Jia, Zhuoran Jia, Zhuxia Jia, Zi-Jun Jia, Zijun Jia, Ziyan Jia, Ziyu Jia, Zongchao Jia
articles
V Papadopoulos, M C Jia, M Culty +2 more · 1993 · In vitro cellular & developmental biology. Animal · Springer · added 2026-04-24
Primary cultures of immature rat Sertoli cells in plastic dishes are highly responsive to follicle stimulating hormone (FSH) and its second messenger, cAMP, in metabolizing testosterone to estradiol, Show more
Primary cultures of immature rat Sertoli cells in plastic dishes are highly responsive to follicle stimulating hormone (FSH) and its second messenger, cAMP, in metabolizing testosterone to estradiol, thus indicating the presence of an active, hormone-regulated aromatase cytochrome P450 (P450arom). However, in vivo studies indicated that P450arom is FSH-responsive only in very young animals, where the cells have not yet differentiated, but they lose this ability later on in development. Sertoli cells grown on Matrigel (a reconstituted basement membrane), laminin (a basement membrane component), or in bicameral chambers coated with Matrigel, assume structural and functional characteristics more similar to that of in vivo differentiated Sertoli cells. When the cells were cultured on laminin or Matrigel, the FSH- and cAMP-induced estradiol production was greatly reduced by 30 and 60%, respectively. When Sertoli cells were cultured in bicameral chambers coated with Matrigel, no induction of testosterone aromatization by FSH or cAMP was observed. However, FSH-induced cAMP formation was greater when the cells were cultured on basement membrane or in the chambers than on plastic dishes. These results suggest that culture conditions favoring the assumption by Sertoli cells of a phenotype closer that of the differentiated cells in vivo (tall columnar and highly polarized) suppress the induction of P450arom by FSH and cAMP. We then examined the mechanism(s) by which cell phenotype affects p450arom activity. Northern blot analyses of Sertoli cell RNA revealed one major band of 1.9 Kb and two minor bands of 3.3 and 5.2 Kb. However, there were no changes at the level of the expression of P450arom messenger RNA under the different culture conditions.(ABSTRACT TRUNCATED AT 250 WORDS) Show less
no PDF DOI: 10.1007/BF02634233
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C M Davis, V Papadopoulos, M C Jia +3 more · 1991 · Experimental cell research · Elsevier · added 2026-04-24
Laminin, a major component of basement membrane extracellular matrices, promotes differentiation in a number of cell types, including Sertoli cells. We have identified and characterized Sertoli cells. Show more
Laminin, a major component of basement membrane extracellular matrices, promotes differentiation in a number of cell types, including Sertoli cells. We have identified and characterized Sertoli cells. We have identified and characterized Sertoli cell surface molecules which interact with laminin. Using laminin-Sepharose affinity chromatography and [125I]laminin binding to Sertoli cell plasma membranes, binding proteins have been identified with the Mr 110,000, 67,000, 55,000, 45,000, 36,000, and 25,000. In addition, the Mr 110,000 and 67,000 laminin binding proteins were phosphorylated. The 67,000, 45,000, and 36,000 react with antibodies to the previously characterized laminin receptor and these antibodies stain the basolateral surface of Sertoli cells in vivo. Cultured Sertoli cells stain for laminin receptor both on the cell surface and within the cells. Antiserum to the 32,000 and 67,000 laminin binding proteins partially inhibited spreading of Sertoli cells on a laminin-coated culture dish, suggesting a functional importance of those proteins in Sertoli cell differentiation. The 25,000 and 45,000 laminin binding proteins reacted with integrin antibodies, but no high-molecular-weight forms could be detected. Integrin was localized to the cell surface and intracellularly but antibodies did not block Sertoli cell spreading on laminin. This work represents the first identification and characterization of extracellular matrix binding proteins in an endocrine organ and suggests an important role for the nonintegrin 32/67 laminin binding proteins. Show less
no PDF DOI: 10.1016/0014-4827(91)90095-c
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M Dym, S Lamsam-Casalotti, M C Jia +2 more · 1991 · Endocrinology · added 2026-04-24
On a basement membrane substrate, Sertoli cells in culture have been shown to assume a phenotype similar to that of the in vivo differentiated cells. Sertoli cells from 10-day-old rats were cultured o Show more
On a basement membrane substrate, Sertoli cells in culture have been shown to assume a phenotype similar to that of the in vivo differentiated cells. Sertoli cells from 10-day-old rats were cultured on plastic and on different extracellular matrix substrates [laminin, a reconstituted basement membrane (Matrigel), and a synthetic laminin peptide containing the arginine-glycine-aspartic acid (RGD) tripeptide sequence] to investigate the effects of the extracellular matrix on FSH responsiveness. Both laminin and Matrigel markedly enhanced the cAMP response to FSH and cholera toxin, indicating modifications at the level of guanine nucleotide-binding regulatory (G) proteins. Furthermore, Sertoli cell grown on either of these two substrates responded to physiological levels of FSH (25-50 ng/ml), whereas pharmacological levels of FSH (500 ng/ml) were required for cells grown on either plastic or on the RGD-containing laminin peptide. Immunoblotting of Sertoli cell plasma membranes with antibodies directed against the alpha-subunit of the stimulatory G-protein (Gs alpha) of adenylyl cyclase indicated that Sertoli cell culture on either laminin or Matrigel increased the amounts of Gs alpha. These results were further confirmed by immunoprecipitating the Gs alpha protein from the particulate fraction of [35S]methionine metabolically labeled Sertoli cells. However, Northern blot analysis using a cDNA probe for Gs alpha did not demonstrate changes in gene expression when Sertoli cells were grown on the various substrates. Immunofluorescent studies revealed that the Gs complex of adenylyl cyclase was preferentially located at the base of the Sertoli cells at the site of contact with the extracellular matrix. These data suggest that culture of epithelial Sertoli cells on basement membrane substrates enhances the Gs complex of adenylyl cyclase and the cAMP response to FSH, consistent with the more differentiated morphology and function of the cells. Show less
no PDF DOI: 10.1210/endo-128-2-1167
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