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TSLP Signaling Network Revealed by Quantitative Phosphoproteomics

机译:通过定量磷蛋白酶揭示的TSLP信号网络

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Thymic stromal lymphopoietin (TSLP) is an IL-7 like cytokine that was originally identified from the conditioned medium of the Z210R.1 thymic stromal cell line. TSLP requires a heterodimeric receptor complex, IL-7 receptor alpha subunit and its unique TSLP receptor (TSLPR, also known CRLF2) to transmit signals into cells. TSLP acts on a number of distinctive cell types and executes various biological functions. Hyperactive TSLP/TSLPR signaling contributes to development of several disorders in humans including asthma and leukemia. However, detailed signal transduction pathways that are responsible for various biological effects of TSLP still remain elusive. Here, we applied the SILAC-based strategy to study the phosphoproteomic changes induced by TSLP as well as induced by leukemic JAK2R683G/TSLPR signaling in cells. Our data shed light on understanding of TSLP signaling pathways and provide potential therapeutic targets for development of novel treatments for TSLP/TSLPR-associated diseases.
机译:胸腺基质淋巴细胞素(TSLP)是IL-7,如细胞因子,其最初鉴定在Z210R.1胸腺基质细胞系的条件培养基中。 TSLP需要异二聚体受体复合物,IL-7受体α亚基及其独特的TSLP受体(TSLPR,也已知的CRLF2)以将信号传递到细胞中。 TSLP采用许多独特的细胞类型并执行各种生物功能。过度活跃的TSLP / TSLPR信号传导有助于在包括哮喘和白血病的人类中的几种疾病的发展有助于开发几种疾病。然而,对TSLP各种生物效应负责的详细信号转导途径仍然难以实现。在这里,我们应用了基于Silac的策略来研究TSLP诱导的磷肝蛋白酶变化以及细胞中白血病JAK2R683G / TSLPR信号传导诱导。我们的数据揭示了对TSLP信号传导途径的理解,并提供潜在的治疗目标,用于开发TSLP / TSLPR-相关疾病的新型治疗方法。

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