Department of Neuroscience, University of Connecticut Health, Farmington, CT, USA.
Department of Neuroscience, University of Texas-Austin, TX, USA.
FEBS Lett. 2024 Oct;598(19):2417-2437. doi: 10.1002/1873-3468.14946. Epub 2024 Jun 10.
C1QL1 is expressed in a subset of cells in the brain and likely has pleiotropic functions, including the regulation of neuron-to-neuron synapses. Research progress on C1QL proteins has been slowed by a dearth of available antibodies. Therefore, we created a novel knock-in mouse line in which an HA-tag is inserted into the endogenous C1ql1 locus. We examined the entire brain, identifying previously unappreciated nuclei expressing C1QL1, presumably in neurons. By total numbers, however, the large majority of C1QL1-expressing cells are of the oligodendrocyte lineage. Subcellular immunolocalization of synaptic cleft proteins is challenging, so we developed a new protocol to improve signal at synapses. Lastly, we compared various anti-HA antibodies to assist future investigations using this and likely other HA epitope-tagged alleles.
C1QL1 在大脑中的一部分细胞中表达,可能具有多种功能,包括调节神经元之间的突触。由于缺乏可用的抗体,C1QL 蛋白的研究进展一直较为缓慢。因此,我们创建了一种新型的基因敲入小鼠品系,其中 HA 标签被插入内源性 C1ql1 基因座。我们检查了整个大脑,鉴定了以前未被发现的表达 C1QL1 的核,这些核可能存在于神经元中。然而,就细胞总数而言,绝大多数表达 C1QL1 的细胞是少突胶质细胞谱系。突触小间隙蛋白的亚细胞免疫定位具有挑战性,因此我们开发了一种新的方案来提高突触处的信号。最后,我们比较了各种抗 HA 抗体,以协助未来使用该抗体及可能的其他 HA 表位标记等位基因进行的研究。