Salian-Mehta Smita, Xu Mei, McKinsey Timothy A, Tobet Stuart, Wierman Margaret E
From the Division of Endocrinology, Metabolism, and Diabetes and.
Division of Cardiology, University of Colorado School of Medicine, Aurora, Colorado 80045.
J Biol Chem. 2015 May 29;290(22):14045-56. doi: 10.1074/jbc.M115.640482. Epub 2015 Apr 14.
The impact of histone deacetylases (HDACs) in the control of gonadotropin releasing hormone (GnRH) neuronal development is unknown. We identified an increase in many HDACs in GT1-7 (differentiated) compared with NLT (undifferentiated) GnRH neuronal cell lines. Increased HDAC9 mRNA and protein and specific deacetylase activity in GT1-7 cells suggested a functional role. Introduction of HDAC9 in NLT cells protected from serum withdrawal induced apoptosis and impaired basal neuronal cell movement. Conversely, silencing of endogenous HDAC9 in GT1-7 cells increased apoptosis and cell movement. Comparison of WT and mutant HDAC9 constructs demonstrated that the HDAC9 pro-survival effects required combined cytoplasmic and nuclear localization, whereas the effects on cell movement required a cytoplasmic site of action. Co-immunoprecipitation demonstrated a novel interaction of HDAC9 selectively with the Class IIb HDAC6. HDAC6 was also up-regulated at the mRNA and protein levels, and HDAC6 catalytic activity was significantly increased in GT1-7 compared with NLT cells. HDAC9 interacted with HDAC6 through its second catalytic domain. Silencing of HDAC6, HDAC9, or both, in GT1-7 cells augmented apoptosis compared with controls. HDAC6 and -9 had additive effects to promote cell survival via modulating the BAX/BCL2 pathway. Silencing of HDAC6 resulted in an activation of movement of GT1-7 cells with induction in acetylation of α-tubulin. Inhibition of HDAC6 and HDAC9 together resulted in an additive effect to increase cell movement but did not alter the acetylation of αtubulin. Together, these studies identify a novel interaction of Class IIa HDAC9 with Class IIb HDAC6 to modulate cell movement and survival in GnRH neurons.
组蛋白去乙酰化酶(HDACs)在促性腺激素释放激素(GnRH)神经元发育调控中的作用尚不清楚。我们发现,与未分化的NLT GnRH神经元细胞系相比,分化的GT1-7细胞中多种HDACs有所增加。GT1-7细胞中HDAC9 mRNA、蛋白及特异性去乙酰化酶活性的增加表明其具有功能性作用。在NLT细胞中引入HDAC9可保护细胞免受血清剥夺诱导的凋亡,并损害基础神经元细胞运动。相反,GT1-7细胞中内源性HDAC9的沉默增加了细胞凋亡和细胞运动。野生型和突变型HDAC9构建体的比较表明,HDAC9的促生存作用需要细胞质和细胞核的联合定位,而对细胞运动的影响则需要细胞质作用位点。免疫共沉淀证明HDAC9与IIb类HDAC6存在新型相互作用。与NLT细胞相比,GT1-7细胞中HDAC6在mRNA和蛋白水平也上调,且HDAC6催化活性显著增加。HDAC9通过其第二个催化结构域与HDAC6相互作用。与对照组相比,GT1-7细胞中HDAC6、HDAC9或二者的沉默均增加了细胞凋亡。HDAC6和-9通过调节BAX/BCL2途径对促进细胞存活具有累加效应。HDAC6的沉默导致GT1-7细胞运动激活,并诱导α-微管蛋白乙酰化。同时抑制HDAC6和HDAC9对增加细胞运动具有累加效应,但不改变α-微管蛋白的乙酰化。总之,这些研究确定了IIa类HDAC9与IIb类HDAC6之间的新型相互作用,以调节GnRH神经元中的细胞运动和存活。