Hendricks Timothy J, Fyodorov Dmitry V, Wegman Lauren J, Lelutiu Nadia B, Pehek Elizabeth A, Yamamoto Bryan, Silver Jerry, Weeber Edwin J, Sweatt J David, Deneris Evan S
Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Neuron. 2003 Jan 23;37(2):233-47. doi: 10.1016/s0896-6273(02)01167-4.
The central serotonin (5-HT) neurotransmitter system is an important modulator of diverse physiological processes and behaviors; however, the transcriptional mechanisms controlling its development are largely unknown. The Pet-1 ETS factor is a precise marker of developing and adult 5-HT neurons and is expressed shortly before 5-HT appears in the hindbrain. Here we show that in mice lacking Pet-1, the majority of 5-HT neurons fail to differentiate. Remaining ones show deficient expression of genes required for 5-HT synthesis, uptake, and storage. Significantly, defective development of the 5-HT system is followed by heightened anxiety-like and aggressive behavior in adults. These findings indicate that Pet-1 is a critical determinant of 5-HT neuron identity and implicate a Pet-1-dependent program in serotonergic modulation of behavior.
中枢5-羟色胺(5-HT)神经递质系统是多种生理过程和行为的重要调节因子;然而,控制其发育的转录机制在很大程度上尚不清楚。Pet-1 ETS因子是发育中和成年5-HT神经元的精确标记物,在5-HT出现在后脑之前不久就开始表达。在这里,我们表明,在缺乏Pet-1的小鼠中,大多数5-HT神经元无法分化。其余的神经元显示出5-HT合成、摄取和储存所需基因的表达缺陷。值得注意的是,5-HT系统的发育缺陷随后导致成年小鼠出现类似焦虑和攻击性行为的增加。这些发现表明,Pet-1是5-HT神经元身份的关键决定因素,并暗示了一个依赖Pet-1的程序参与5-羟色胺能对行为的调节。