de Lombares Camille, Heude Eglantine, Alfama Gladys, Fontaine Anastasia, Hassouna Rim, Vernochet Cécile, de Chaumont Fabrice, Olivo-Marin Christophe, Ey Elodie, Parnaudeau Sébastien, Tronche François, Bourgeron Thomas, Luquet Serge, Levi Giovanni, Narboux-Nême Nicolas
Physiologie Moléculaire et Adaptation, CNRS UMR7221, Muséum National d'Histoire Naturelle, Département AVIV, Paris, France.
Unité de Biologie Fonctionnelle et Adaptative (BFA), Université Paris Diderot, Sorbonne Paris Cité, CNRS UMR 8251, Paris, France.
Aging (Albany NY). 2019 Sep 12;11(17):6638-6656. doi: 10.18632/aging.102141.
and encode two homeobox transcription factors expressed by developing and mature GABAergic interneurons. During development, play a role in the differentiation of certain GABAergic subclasses. Here we address the question of the functional role of Dlx5/6 in the mature central nervous system. First, we demonstrate that and are expressed by all subclasses of adult cortical GABAergic neurons. Then we analyze mice in which and are simultaneously inactivated in all GABAergic interneurons. mice present a behavioral pattern suggesting reduction of anxiety-like behavior and obsessive-compulsive activities, and a lower interest in nest building. Twenty-month-old animals have the same size as their normal littermates, but present a 25% body weight reduction associated with a marked decline in white and brown adipose tissue. Remarkably, both and mice present a 33% longer median survival. Hallmarks of biological aging such as motility, adiposity and coat conditions are improved in mutant animals. Our data imply that GABAergic interneurons can regulate healthspan and lifespan through -dependent mechanisms. Understanding these regulations can be an entry point to unravel the processes through which the brain affects body homeostasis and, ultimately, longevity and healthy aging.
并编码两种由发育中和成熟的γ-氨基丁酸能中间神经元表达的同源框转录因子。在发育过程中,它们在某些γ-氨基丁酸能亚类的分化中发挥作用。在这里,我们探讨Dlx5/6在成熟中枢神经系统中的功能作用问题。首先,我们证明Dlx5/6由成年皮质γ-氨基丁酸能神经元的所有亚类表达。然后我们分析在所有γ-氨基丁酸能中间神经元中Dlx5和Dlx6同时失活的小鼠。Dlx5/6双敲除小鼠呈现出一种行为模式,表明焦虑样行为和强迫行为减少,对筑巢的兴趣降低。20个月大的Dlx5/6双敲除动物与正常同窝小鼠大小相同,但体重减轻了25%,同时白色和棕色脂肪组织显著减少。值得注意的是,Dlx5和Dlx6单敲除小鼠的中位生存期均延长了33%。突变动物的生物衰老特征,如运动能力、肥胖和皮毛状况都得到了改善。我们的数据表明,γ-氨基丁酸能中间神经元可以通过依赖Dlx5/6的机制调节健康寿命和寿命。了解这些调节机制可能是揭示大脑影响身体稳态以及最终影响长寿和健康衰老过程的切入点。