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首页> 外文期刊>The biochemical journal >Peroxisome-proliferator-activated receptor-binding protein (PBP) is essential for the growth of active Notch4-immortalized mammary epithelial cells by activating SOX10 expression
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Peroxisome-proliferator-activated receptor-binding protein (PBP) is essential for the growth of active Notch4-immortalized mammary epithelial cells by activating SOX10 expression

机译:过氧化物酶体增殖物激活受体结合蛋白(PBP)通过激活SOX10表达对于Notch4永生化的乳腺上皮细胞的生长至关重要

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pPBP (peroxisome-proliferator-activated receptor-binding protein) [Med1 (mediator 1)/TRAP220 (thyroid-hormone-receptor-associated protein 220)] is essential for mammary gland development. We established a mammary epithelial cell line with a genotype of PBPsupLoxP/LoxP/sup by expressing an active form of Notch4. Null mutation of PBP caused severe growth inhibition of the Notch4-immortalized mammary cells. We found that truncated PBP without the two LXXLL motifs could reverse the growth inhibition due to the deficiency of endogenous PBP, indicating that signalling through nuclear receptors is unlikely to be responsible for the growth inhibition as the result of PBP deficiency. Loss of PBP expression was shown to completely ablate the expression of SOX10 [Sry-related HMG (high-mobility group) box gene 10]. The re-expression of SOX10 was capable of reversing the growth inhibition due to PBP deficiency, whereas suppressed expression of SOX10 inhibited the growth of Notch4-immortalized mammary cells. Further studies revealed PBP is directly recruited to the enhancer of the iSOX10/i gene, indicating that SOX10 is a direct target gene of PBP. We conclude that PBP is essential for the growth of Notch4-immortalized mammary cells by activating SOX10 expression, providing a potential molecular mechanism through which PBP regulates the growth of mammary stem/progenitor cells./p
机译:PBP(过氧化物酶体-增殖物激活的受体结合蛋白)[Med1(介体1)/ TRAP220(甲状腺激素受体相关蛋白220)]对乳腺发育至关重要。通过表达Notch4的活性形式,我们建立了具有PBP LoxP / LoxP 基因型的乳腺上皮细胞系。 PBP的无效突变导致Notch4永生化的乳腺细胞受到严重的生长抑制。我们发现,由于缺乏内源性PBP,没有两个LXXLL基序的截短的PBP可以逆转生长抑制,这表明通过核受体的信号传导不太可能是PBP缺乏导致生长抑制的原因。显示PBP表达的丧失完全消除了SOX10 [Sry相关的HMG(高迁移率组)盒基因10]的表达。 SOX10的重新表达能够逆转由于PBP缺乏引起的生长抑制,而SOX10的抑制表达则抑制了Notch4永生化乳腺细胞的生长。进一步的研究表明PBP被直接募集到 SOX10 基因的增强子中,表明SOX10是PBP的直接靶基因。我们得出的结论是,PBP通过激活SOX10表达对于Notch4永生化的乳腺细胞的生长至关重要,提供了潜在的分子机制,通过PBP调控乳腺干/祖细胞的生长。

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