Instituto de Investigaciones Biomédicas, CSIC-UAM, Arturo Duperier 4, 28029-Madrid, Spain.
Glia. 2011 Feb;59(2):293-307. doi: 10.1002/glia.21101.
Peroxisome proliferator-activated receptor gamma (PPARγ) belongs to a family of ligand-activated nuclear receptors and its ligands are known to control many physiological and pathological situations. Its role in the central nervous system has been under intense analysis during the last years. Here we show a novel function for PPARγ in controlling stem cell expansion in the adult mammalian brain. Adult rats treated with pioglitazone, a specific ligand of PPARγ, had elevated numbers of proliferating progenitor cells in the subventricular zone and the rostral migratory stream. Electron microscopy analysis also showed important changes in the subventricular zone ultrastructure of pioglitazone-treated animals including an increased number of migratory cell chains. These results were further confirmed in vitro. Neurosphere assays revealed significant increases in the number of neurosphere forming cells from pioglitazone- and rosiglitazone (two specific ligands of PPARγ receptor)-treated cultures that exhibited enhanced capacity for cell migration and differentiation. The effects of pioglitazone were blocked by the PPARγ receptor antagonists GW9662 and T0070907, suggesting that its effects are mediated by a mechanism dependent on PPARγ activation. These results indicate for the first time that activation of PPARγ receptor directly regulates proliferation, differentiation, and migration of neural stem cells in vivo.
过氧化物酶体增殖物激活受体γ(PPARγ)属于配体激活的核受体家族,其配体已知可控制许多生理和病理情况。近年来,其在中枢神经系统中的作用受到了深入分析。在这里,我们展示了 PPARγ 在控制成年哺乳动物大脑中的干细胞扩增中的新功能。用吡格列酮(PPARγ 的特异性配体)处理的成年大鼠在侧脑室下区和额迁移流中有更多的增殖祖细胞。电子显微镜分析还显示,吡格列酮处理动物的侧脑室下区超微结构发生了重要变化,包括迁移细胞链的数量增加。这些结果在体外得到了进一步证实。神经球测定显示,来自吡格列酮和罗格列酮(PPARγ 受体的两种特异性配体)处理的培养物的神经球形成细胞数量显著增加,这些细胞表现出增强的迁移和分化能力。吡格列酮的作用被 PPARγ 受体拮抗剂 GW9662 和 T0070907 阻断,表明其作用是通过依赖于 PPARγ 激活的机制介导的。这些结果首次表明,PPARγ 受体的激活可直接调节体内神经干细胞的增殖、分化和迁移。