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半乳糖凝集素-4与CD14的相互作用通过丝裂原活化蛋白激酶信号通路触发单核细胞分化为巨噬细胞样细胞。

Galectin-4 Interaction with CD14 Triggers the Differentiation of Monocytes into Macrophage-like Cells via the MAPK Signaling Pathway.

作者信息

Hong So-Hee, Shin Jun-Seop, Chung Hyunwoo, Park Chung-Gyu

机构信息

Xenotransplantation Research Center, Seoul National University College of Medicine, Seoul 03080, Korea.

Institute of Endemic Diseases, Seoul National University College of Medicine, Seoul 03080, Korea.

出版信息

Immune Netw. 2019 May 29;19(3):e17. doi: 10.4110/in.2019.19.e17. eCollection 2019 Jun.

Abstract

Galectin-4 (Gal-4) is a β-galactoside-binding protein mostly expressed in the gastrointestinal tract of animals. Although intensive functional studies have been done for other galectin isoforms, the immunoregulatory function of Gal-4 still remains ambiguous. Here, we demonstrated that Gal-4 could bind to CD14 on monocytes and induce their differentiation into macrophage-like cells through the MAPK signaling pathway. Gal-4 induced the phenotypic changes on monocytes by altering the expression of various surface molecules, and induced functional changes such as increased cytokine production and matrix metalloproteinase expression and reduced phagocytic capacity. Concomitant with these changes, Gal-4-treated monocytes became adherent and showed elongated morphology with higher expression of macrophage markers. Notably, we found that Gal-4 interacted with CD14 and activated the MAPK signaling cascade. Therefore, these findings suggest that Gal-4 may exert the immunoregulatory functions through the activation and differentiation of monocytes.

摘要

半乳糖凝集素-4(Gal-4)是一种β-半乳糖苷结合蛋白,主要在动物胃肠道中表达。尽管已对其他半乳糖凝集素异构体进行了深入的功能研究,但Gal-4的免疫调节功能仍不明确。在此,我们证明Gal-4可与单核细胞上的CD14结合,并通过丝裂原活化蛋白激酶(MAPK)信号通路诱导其分化为巨噬细胞样细胞。Gal-4通过改变各种表面分子的表达诱导单核细胞的表型变化,并诱导功能变化,如细胞因子产生增加、基质金属蛋白酶表达增加和吞噬能力降低。伴随着这些变化,经Gal-4处理的单核细胞变得黏附,并呈现出伸长的形态,巨噬细胞标志物的表达更高。值得注意的是,我们发现Gal-4与CD14相互作用并激活MAPK信号级联反应。因此,这些发现表明Gal-4可能通过单核细胞的激活和分化发挥免疫调节功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f2/6597441/4bdbcd34f9f8/in-19-e17-g001.jpg

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