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Thy-1 通过 PPARγ 信号促进肺发育过程中的脂肪成纤维细胞分化。

Thy-1 signals through PPARγ to promote lipofibroblast differentiation in the developing lung.

机构信息

Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave., Cincinnati, OH 45229, USA.

出版信息

Am J Respir Cell Mol Biol. 2012 Jun;46(6):765-72. doi: 10.1165/rcmb.2011-0316OC. Epub 2012 Jan 20.

Abstract

Thy-1 is a glycosylphosphytidylinositol-linked cell-surface glycoprotein present on a subset of lung fibroblasts, which plays an important role in postnatal alveolarization. In the present study, we define the role of Thy-1 in pulmonary lipofibroblast differentiation and in the regulation of lipid homeostasis via peroxisome proliferator-activated receptor-γ (PPARγ). Thy-1 was associated with interstitial cells containing lipid droplets in vivo. The transfection of Thy-1 into Thy-1 (-) fibroblasts increased triglyceride content, fatty-acid uptake, and the expression of the lipofibroblast marker adipocyte differentiation-related protein. Thy-1 (+) fibroblasts exhibited 2.4-fold higher PPARγ activity, and the inhibition or activation of PPARγ reduced and increased triglyceride content, respectively. Thy-1 (-) fibroblasts were not responsive to either of the PPARγ agonists ciglitazone or prostaglandin J(2), supporting the importance of Thy-1 in signaling via PPARγ. Thy-1 (+) fibroblasts expressed significantly higher concentrations of fatty-acid transporter protein-3 mRNA, and demonstrated higher rates of fatty-acid uptake and increased triglyceride content. The inhibition of fatty-acid transporter protein function reduced Thy-1 (+) fibroblast lipid content. The expression of Thy-1 in C57BL/6 lung fibroblasts increased during the neonatal period, coinciding with the onset of alveolarization. Thy-1 promoted lipofibroblast differentiation via the expression of PPARγ, stimulated lipid accumulation via fatty-acid esterification, and enhanced the fatty-acid uptake mediated by fatty-acid transporter proteins. Thy-1 is important in the regulation of lipofibroblast differentiation in the developing lung.

摘要

Thy-1 是一种糖基磷脂酰肌醇连接的细胞表面糖蛋白,存在于一部分肺成纤维细胞上,在出生后肺泡化过程中发挥重要作用。本研究旨在探讨 Thy-1 在肺脂肪成纤维细胞分化中的作用及其对脂代谢平衡的调控机制,特别是通过过氧化物酶体增殖物激活受体-γ(PPARγ)。研究发现 Thy-1 与体内含有脂滴的间质细胞有关。将 Thy-1 转染到 Thy-1(-)成纤维细胞中,可增加甘油三酯含量、脂肪酸摄取和脂肪分化相关蛋白的表达。Thy-1(+)成纤维细胞中 PPARγ 活性增加 2.4 倍,PPARγ 的抑制或激活分别降低和增加甘油三酯含量。Thy-1(-)成纤维细胞对 PPARγ 激动剂 ciglitazone 或前列腺素 J2 均无反应,提示 Thy-1 在 PPARγ 信号转导中起重要作用。Thy-1(+)成纤维细胞脂肪酸转运蛋白-3mRNA 表达水平显著升高,表现为脂肪酸摄取率增加和甘油三酯含量增加。脂肪酸转运蛋白功能抑制降低了 Thy-1(+)成纤维细胞的脂质含量。C57BL/6 肺成纤维细胞中 Thy-1 的表达在新生儿期增加,与肺泡化开始时间一致。Thy-1 通过表达 PPARγ 促进脂肪成纤维细胞分化,通过脂肪酸酯化刺激脂质积累,并增强脂肪酸转运蛋白介导的脂肪酸摄取。Thy-1 在调节肺成纤维细胞分化中起重要作用。

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