Longan Luz, Longnecker Richard
Department of Microbiology-Immunology, Northwestern University Medical School, 303 E. Chicago Avenue, Chicago, IL 60611, USA1.
J Gen Virol. 2000 Sep;81(Pt 9):2245-2252. doi: 10.1099/0022-1317-81-9-2245.
Previous studies using transgenic mice with B-cell expression of LMP2A demonstrated that LMP2A drives B-cell development and survival signal in the absence of normal B-cell receptor (BCR) signal transduction. To determine if LMP2A may have similar effects in epithelial differentiation, six transgenic murine lines were constructed and analysed with LMP2A expression directed to the epidermis by a keratin 14 (K14) promoter cassette. LMP2A protein expression was verified by immunofluorescence and immunoprecipitation of skin samples using LMP2A-specific antibodies. To evaluate the effects of LMP2A expression on epidermal differentiation, immunofluorescence and histochemistry were performed on tongue and tail samples of transgenic mice and their wild-type littermate controls using differentially expressed keratins. The analysis indicated that LMP2A does not alter the normal epithelial differentiation program in the epithelia of K14-LMP2A transgenic mice.
以往使用在B细胞中表达LMP2A的转基因小鼠进行的研究表明,在缺乏正常B细胞受体(BCR)信号转导的情况下,LMP2A驱动B细胞的发育和存活信号。为了确定LMP2A在上皮分化中是否可能具有类似作用,构建了六个转基因鼠系,并通过角蛋白14(K14)启动子盒将LMP2A表达定向到表皮进行分析。使用LMP2A特异性抗体通过免疫荧光和皮肤样品的免疫沉淀来验证LMP2A蛋白表达。为了评估LMP2A表达对表皮分化的影响,使用差异表达的角蛋白对转基因小鼠及其野生型同窝对照的舌头和尾巴样品进行免疫荧光和组织化学分析。分析表明,LMP2A不会改变K14-LMP2A转基因小鼠上皮中的正常上皮分化程序。