Nojima Kojiro, Miyazaki Haruko, Hori Tetsuya, Vargova Lydia, Oohashi Toshitaka
Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Cellular and Molecular Synaptic Function Unit, Okinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
Front Cell Dev Biol. 2021 Sep 17;9:730550. doi: 10.3389/fcell.2021.730550. eCollection 2021.
The calyx of Held is a giant nerve terminal mediating high-frequency excitatory input to principal cells of the medial nucleus of the trapezoid body (MNTB). MNTB principal neurons are enwrapped by densely organized extracellular matrix structures, known as perineuronal nets (PNNs). Emerging evidence indicates the importance of PNNs in synaptic transmission at the calyx of Held. Previously, a unique differential expression of aggrecan and brevican has been reported at this calyceal synapse. However, the role of hyaluronan and proteoglycan binding link proteins (HAPLNs) in PNN formation and synaptic transmission at this synapse remains elusive. This study aimed to assess immunohistochemical evidence for the effect of HAPLN4 on differential PNN formation at the calyx of Held. Genetic deletion of exhibited a clear ectopic shift of brevican localization from the perisynaptic space between the calyx of Held terminals and principal neurons to the neuropil surrounding the whole calyx of Held terminals. In contrast, aggrecan expression showed a consistent localization at the surrounding neuropil, together with HAPLN1 and tenascin-R, in both gene knockout (KO) and wild-type (WT) mice. An proximity ligation assay demonstrated the molecular association of brevican with HAPLN4 in WT and HAPLN1 in gene KO mice. Further elucidation of the roles of HAPLN4 may highlight the developmental and physiological importance of PNN formation in the calyx of Held.
Held壶腹是一个巨大的神经末梢,介导对梯形体内侧核(MNTB)主细胞的高频兴奋性输入。MNTB主神经元被密集组织的细胞外基质结构包裹,称为神经元周围网(PNNs)。新出现的证据表明PNNs在Held壶腹的突触传递中很重要。此前,已报道在这个壶腹突触处聚集蛋白聚糖和短蛋白聚糖存在独特的差异表达。然而,透明质酸和蛋白聚糖结合连接蛋白(HAPLNs)在这个突触处的PNN形成和突触传递中的作用仍然不清楚。本研究旨在评估HAPLN4对Held壶腹处差异PNN形成影响的免疫组化证据。基因敲除显示短蛋白聚糖的定位从Held壶腹末梢与主神经元之间的突触周围空间明显异位转移到围绕整个Held壶腹末梢的神经毡。相比之下,在基因敲除(KO)小鼠和野生型(WT)小鼠中,聚集蛋白聚糖的表达在周围神经毡以及HAPLN1和腱生蛋白-R处显示出一致的定位。一种接近连接分析证明了野生型小鼠中短蛋白聚糖与HAPLN4以及基因敲除小鼠中短蛋白聚糖与HAPLN1之间的分子关联。对HAPLN4作用的进一步阐明可能会突出PNN在Held壶腹形成中的发育和生理重要性。