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INDUCTION OF BROWN ADIPOCYTES BY TRANSCRIPTION FACTOR NFE2L2

机译:转录因子NFE2L2诱导棕色脂肪细胞

摘要

New methods have been developed to treat obesity or other human disorders by increasing the degree of brown adipose thermogenesis, by both increasing the growth and differentiation of brown adipose tissue and increasing its activity. A new use for the transcription factor NFE2l2 was developed to increase BAT thermogenesis by increasing the expression of Ucp1. For the first time, NFE2l2 was found to interact with the NF-E2 motif and to stimulate the expression of Ucp1 (Figure 9). By modulating the expression of the Nfe2l2 gene or the concentration of NFE2l2 protein, changes in brown adipose tissue thermogenesis can be achieved to treat various weight disorders. Additionally, the direct involvement of CREB binding to CRE2 to regulate Ucp1 expression was demonstrated. Furthermore, transient transfection assays of luciferase reporter constructs and site-directed mutagenesis indicated that CRE2 was involved in transcriptional regulation of the Ucp1 through interaction with a phosphorylated CREB. NFE2l2 can be combined with other known transcription factors, e.g., CREB, PGC1, RXR, RAR, and PPAR gamma, to increase BAT thermogenesis by increasing the expression of Ucp1.
机译:已经开发了通过增加棕色脂肪生热的程度,通过增加棕色脂肪组织的生长和分化以及增加其活性来治疗肥胖症或其他人类疾病的新方法。转录因子NFE2l2的新用途已被开发出来,可通过增加Ucp1的表达来增加BAT生热作用。首次发现NFE212与NF-E2基序相互作用并刺激Ucp1的表达(图9)。通过调节Nfe2l2基因的表达或NFE2l2蛋白的浓度,可以改变棕色脂肪组织的生热作用,以治疗各种体重异常。此外,证明了CREB与CRE2结合直接参与调节Ucp1表达。此外,荧光素酶报告基因构建体的瞬时转染测定和定点诱变表明,CRE2通过与磷酸化CREB的相互作用参与了Ucp1的转录调控。 NFE212可以与其他已知的转录因子(例如CREB,PGC1,RXR,RAR和PPARγ)结合使用,以通过增加Ucp1的表达来增加BAT生热作用。

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