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LGI3 通过 Akt 通路促进人角质形成细胞分化。

LGI3 promotes human keratinocyte differentiation via the Akt pathway.

机构信息

Department of Biochemistry, Chung-Ang University College of Medicine, Seoul, Korea.

出版信息

Exp Dermatol. 2018 Nov;27(11):1224-1229. doi: 10.1111/exd.13766. Epub 2018 Sep 12.

Abstract

Leucine-rich repeat LGI family member 3 (LGI3), a member of the LGI family, is a secreted protein that is expressed not only in the brain and adipose tissues, but also in various skin cells. We previously reported that LGI3 was secreted after exposure to ultraviolet B and promoted the migration of HaCaT human keratinocytes. In the present study, we investigated whether LGI3 influences the differentiation of keratinocytes. The results show that the expression of involucrin, a keratinocyte differentiation marker, was reduced in tissue from LGI3-knockout mice. Those results indicate that LGI3 plays an important role in keratinocyte differentiation. Therefore, we treated HaCaT cells with LGI3 to examine its effect on keratinocyte differentiation. Protein levels of various differentiation markers were enhanced by treatment with LGI3. Furthermore, expression of differentiation markers was inhibited when keratinocytes were transfected with an siRNA for LGI3. LGI3 strongly activated Akt, whereas it had no apparent effect on extracellular signal-regulated kinase, p38 mitogen-activated protein kinase, or the c-Jun N-terminal kinase. A specific inhibitor of phosphoinositide 3-kinase, LY294002, reduced LGI3-induced expression of differentiation markers in HaCaT cells. Taken together, these results suggest that LGI3 promotes keratinocyte differentiation and could be used as a therapeutic agent to recover skin barrier function in epidermal barrier disruption.

摘要

富含亮氨酸重复 LGI 家族成员 3(LGI3)是 LGI 家族的成员,是一种分泌蛋白,不仅在大脑和脂肪组织中表达,而且在各种皮肤细胞中表达。我们之前报道过,LGI3 在暴露于紫外线 B 后被分泌,并促进 HaCaT 人角质形成细胞的迁移。在本研究中,我们研究了 LGI3 是否影响角质形成细胞的分化。结果表明,角质形成细胞分化标志物内披蛋白的表达在 LGI3 敲除小鼠的组织中减少。这些结果表明 LGI3 在角质形成细胞分化中发挥重要作用。因此,我们用 LGI3 处理 HaCaT 细胞,以研究其对角质形成细胞分化的影响。各种分化标志物的蛋白水平通过 LGI3 处理得到增强。此外,当角质形成细胞用针对 LGI3 的 siRNA 转染时,分化标志物的表达受到抑制。LGI3 强烈激活 Akt,但对细胞外信号调节激酶、p38 丝裂原活化蛋白激酶或 c-Jun N-末端激酶没有明显影响。PI3K 的特异性抑制剂 LY294002 降低了 HaCaT 细胞中 LGI3 诱导的分化标志物的表达。总之,这些结果表明 LGI3 促进角质形成细胞分化,可作为恢复表皮屏障破坏中皮肤屏障功能的治疗剂。

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