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Jagged-1 mediated activation of notch signaling induces complete maturation of human keratinocytes through NF-kappaB and PPARgamma.

机译:Jagged-1介导的Notch信号的激活通过NF-κB和PPARγ诱导人角质形成细胞完全成熟。

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Establishing an effective epidermal barrier requires a series of coordinated molecular events involving keratinocytes (KCs) within a stratified epithelium. Epidermal maturation depends on convergence of pathways involving components of NF-kappaB and peroxisome proliferator activated receptor (PPAR) signaling systems that promote terminal differentiation and production of a stratum corneum. The Notch-1 receptor and its ligand Delta-1 have been proposed by others to participate in early events in KC differentiation. Here, we establish differential expression patterns for several Notch receptors and ligands in normal human skin. These immunolocalization findings, together with functional studies demonstrating increased levels of Notch ligand/receptors occurring during the onset of differentiation, prompted use of a soluble Notch ligand, a peptide derived from the most conspicuously expressed ligand in skin, Jagged-1. Exposing submerged KC monolayers to this peptide (JAG-1) in co-presence of elevated calcium ion concentration, produced stratification with loricrin expression. Using a living human epidermal equivalent (EE) model system, when submerged cultures were raised to an air/liquid interface to generate a fully mature epidermis, activation of Notch signaling was detected. Addition of JAG-1 peptide to submerged EEs was sufficient to induce epidermal maturation. Moreover, a soluble decoy Notch inhibitor prevented such differentiation and corneogenesis in human EEs exposed to either an air/liquid interface or to the JAG-1 peptide. In KC monolayers, addition of JAG-1 peptide induced IKKalpha mediated NF-kappaB activation, as well as increased PPARgamma expression. Immunoprecipitation/Western blot analysis revealed a physical association between the p65 subunit of NF-kappaB and PPARgamma. These results indicate that activation of Notch signaling is necessary for maturation of human epidermis, and activation by a soluble Notch ligand is sufficient to trigger complete KC differentiation including cornification. doi:10.1038/sj.cdd.4401036
机译:建立有效的表皮屏障需要一系列协调的分子事件,包括分层上皮内的角质形成细胞(KC)。表皮的成熟取决于涉及NF-κB和过氧化物酶体增殖物激活受体(PPAR)信号传导系统的信号通路的融合,该信号传导系统促进终末分化和角质层的产生。其他人已提出Notch-1受体及其配体Delta-1参与KC分化的早期事件。在这里,我们建立了正常人类皮肤中几种Notch受体和配体的差异表达模式。这些免疫定位的发现以及功能研究表明分化开始期间出现的Notch配体/受体水平升高,促使人们使用可溶性Notch配体,该肽是皮肤中最明显表达的配体Jagged-1衍生的肽。在钙离子浓度升高的情况下,将浸没的KC单分子层暴露于该肽(JAG-1)会产生分层,并带有loricrin表达。使用活的人类表皮当量(EE)模型系统,当将淹没的培养物提升至空气/液体界面以产生完全成熟的表皮时,就检测到Notch信号的激活。将JAG-1肽添加到浸没的EE中足以诱导表皮成熟。而且,可溶性诱饵Notch抑制剂阻止了暴露于空气/液体界面或JAG-1肽的人EE中的这种分化和角质形成。在KC单层中,添加JAG-1肽会诱导IKKalpha介导的NF-kappaB激活,以及增加的PPARgamma表达。免疫沉淀/蛋白质印迹分析揭示了NF-κB的p65亚基和PPARγ之间的物理联系。这些结果表明,Notch信号的激活对于人类表皮的成熟是必要的,并且可溶性Notch配体的激活足以触发包括角质形成在内的完全KC分化。 doi:10.1038 / sj.cdd.4401036

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