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Molecular characterization of three gonad cell lines.

机译:三种性腺细胞系的分子表征。

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To facilitate the study of the regulation and downstream interactions of genes involved in gonad development it is important to have a suitable cell culture model. We therefore aimed to characterize molecularly three different mouse gonad cell lines. TM3 and TM4 cells were originally isolated from prepubertal mouse gonads and were tentatively identified as being of Leydig cell and Sertoli cell origin, respectively, based upon their morphology and hormonal responses. The third line is a conditionally immortalized cell line, derived from 10.5-11.5 days post-coitum (dpc) male gonads of transgenic embryos carrying a temperature-sensitive SV40 large T-antigen. We studied by reverse transcription-polymerase chain reaction (RT-PCR) the expression profiles of a number of genes known to be important for early gonad development. Moreover, we assessed these cell lines for their capacity to induce SOX9 transcription upon expression of SRY, a key molecular event occurring during sex determination. We found that allthree cell lines were unable to upregulate SOX9 expression upon transfection of SRY-expression constructs, even though these cells express many of the studied embryonic gonad genes. These observations point to a requirement for SRY cofactors for direct or indirect upregulation of SOX9 expression during testis determination.
机译:为了促进对性腺发育中涉及的基因的调控和下游相互作用的研究,拥有合适的细胞培养模型非常重要。因此,我们旨在表征三种不同的小鼠性腺细胞系。 TM3和TM4细胞最初是从青春期前的小鼠性腺中分离出来的,并根据它们的形态和激素反应,分别被初步确定为Leydig细胞和Sertoli细胞的起源。第三系是有条件永生化的细胞系,衍生自带有温度敏感的SV40大T抗原的转基因胚胎的房顶后(dpc)雄性腺的10.5-11.5天。我们通过逆转录聚合酶链反应(RT-PCR)研究了许多已知对性腺早期发育很重要的基因的表达谱。此外,我们评估了这些细胞系在SRY表达后诱导SOX9转录的能力,SRY是性别确定期间发生的关键分子事件。我们发现所有三种细胞系在SRY表达构建体转染后均无法上调SOX9表达,即使这些细胞表达了许多已研究的胚胎性腺基因。这些观察结果表明在睾丸测定过程中需要SRY辅助因子直接或间接上调SOX9的表达。

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