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上皮细胞过氧化物酶体增殖物激活受体γ有助于正常肺成熟。

Epithelial cell PPAR[gamma] contributes to normal lung maturation.

作者信息

Simon Dawn M, Arikan Meltem C, Srisuma Sorachai, Bhattacharya Soumyaroop, Tsai Larry W, Ingenito Edward P, Gonzalez Frank, Shapiro Steven D, Mariani Thomas J

机构信息

Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Harvard Medical School, Thorn 908, 75 Francis St., Boston, Massachusetts 02115, USA.

出版信息

FASEB J. 2006 Jul;20(9):1507-9. doi: 10.1096/fj.05-5410fje. Epub 2006 May 23.

Abstract

Peroxisome proliferator-activated receptor (PPAR)-gamma is a member of the nuclear hormone receptor superfamily that can promote cellular differentiation and organ development. PPARgamma expression has been reported in a number of pulmonary cell types, including inflammatory, mesenchymal, and epithelial cells. We find that PPARgamma is prominently expressed in the airway epithelium in the mouse lung. In an effort to define the physiological role of PPARgamma within the lung, we have ablated PPARgamma using a novel line of mice capable of specifically targeting the airway epithelium. Airway epithelial cell PPARgamma-targeted mice display enlarged airspaces resulting from insufficient postnatal lung maturation. The increase in airspace size is accompanied by alterations in lung physiology, including increased lung volumes and decreased tissue resistance. Genome-wide expression profiling reveals a reduction in structural extracellular matrix (ECM) gene expression in conditionally targeted mice, suggesting a disruption in epithelial-mesenchymal interactions necessary for the establishment of normal lung structure. Expression profiling of airway epithelial cells isolated from conditionally targeted mice indicates PPARgamma regulates genes encoding known PPARgamma targets, additional lipid metabolism enzymes, and markers of cellular differentiation. These data reveal airway epithelial cell PPARgamma is necessary for normal lung structure and function.

摘要

过氧化物酶体增殖物激活受体(PPAR)-γ是核激素受体超家族的成员,可促进细胞分化和器官发育。PPARγ已在多种肺细胞类型中被报道表达,包括炎症细胞、间充质细胞和上皮细胞。我们发现PPARγ在小鼠肺脏的气道上皮中显著表达。为了确定PPARγ在肺内的生理作用,我们利用一种能够特异性靶向气道上皮的新型小鼠品系敲除了PPARγ。气道上皮细胞PPARγ靶向敲除的小鼠出现因出生后肺成熟不足导致的气腔增大。气腔大小的增加伴随着肺生理功能的改变,包括肺容积增加和组织阻力降低。全基因组表达谱分析显示,条件性靶向敲除小鼠的结构细胞外基质(ECM)基因表达减少,提示正常肺结构建立所需的上皮-间充质相互作用受到破坏。从条件性靶向敲除小鼠分离的气道上皮细胞的表达谱分析表明,PPARγ调节编码已知PPARγ靶标的基因、其他脂质代谢酶以及细胞分化标志物。这些数据揭示气道上皮细胞PPARγ对正常肺结构和功能是必需的。

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