Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT, USA.
Department of Molecular Biology, Universitätsmedizin Göttingen, Göttingen, Germany.
J Neurochem. 2021 May;157(4):1032-1051. doi: 10.1111/jnc.15270. Epub 2021 Jan 5.
Collybistin (CB) is a guanine nucleotide exchange factor (GEF) selectively localized at GABAergic and glycinergic postsynapses. Analysis of mRNA shows that several isoforms of collybistin are expressed in the brain. Some of the isoforms have a SH3 domain (CBSH3+) and some have no SH3 domain (CBSH3-). The CBSH3+ mRNAs are predominantly expressed over CBSH3-. However, in an immunoblot study of mouse brain homogenates, only CBSH3+ protein isoforms were detected, proposing that CBSH3- protein might not be expressed in the brain. The expression or lack of expression of CBSH3- protein is an important issue because CBSH3- has a strong effect in promoting the postsynaptic clustering of gephyrin and GABA-A receptors (GABA Rs). Moreover CBSH3- is constitutively active; therefore lower expression of CBSH3- protein might play a relatively stronger functional role than the more abundant but self-inhibited CBSH3+ isoforms, which need to be activated. We are now showing that: (a) CBSH3- protein is expressed in the brain; (b) parvalbumin positive (PV+) interneurons show higher expression of CBSH3- protein than other neurons; (c) CBSH3- is associated with GABAergic synapses in various regions of the brain and (d) knocking down CBSH3- in hippocampal neurons decreases the synaptic clustering of gephyrin and GABA Rs. The results show that CBSH3- protein is expressed in the brain and that it plays a significant role in the size regulation of the GABAergic postsynapse.
脑啡肽酶(CB)是一种鸟嘌呤核苷酸交换因子(GEF),选择性地定位于 GABA 能和甘氨酸能突触后。对 mRNA 的分析表明,脑啡肽酶有几种异构体在脑中表达。有些异构体具有 SH3 结构域(CBSH3+),有些则没有 SH3 结构域(CBSH3-)。CBSH3+mRNA 主要在 CBSH3-上表达。然而,在对小鼠脑匀浆的免疫印迹研究中,只检测到 CBSH3+蛋白异构体,这表明 CBSH3-蛋白可能不在脑中表达。CBSH3-蛋白的表达或缺失是一个重要问题,因为 CBSH3-在促进 gephyrin 和 GABA-A 受体(GABA Rs)的突触后聚集方面具有很强的作用。此外,CBSH3-是组成性激活的;因此,CBSH3-蛋白的低表达可能比更丰富但自我抑制的 CBSH3+异构体发挥更强的功能作用,后者需要被激活。我们现在表明:(a)CBSH3-蛋白在脑中表达;(b)parvalbumin 阳性(PV+)中间神经元比其他神经元表达更高水平的 CBSH3-蛋白;(c)CBSH3-与脑内不同区域的 GABA 能突触相关;(d)在海马神经元中敲低 CBSH3-会减少 gephyrin 和 GABA Rs 的突触聚集。结果表明 CBSH3-蛋白在脑中表达,并在 GABA 能突触的大小调节中发挥重要作用。