Ikuta Rio, Kakinohana Yuu, Hamada Shun
International College of Arts and Sciences, Fukuoka Women's University, 1-1-1, Kasumigaoka, Higashi-Ku, Fukuoka 813-8529, Japan.
Chem Senses. 2024 Jan 1;49. doi: 10.1093/chemse/bjae019.
Taste receptor cells are morphologically classified as types II and III. Type II cells form a unique type of synapses referred to as channel synapses where calcium homeostasis modulator 1 (CALHM1) together with CALHM3 forms voltage-gated channels that release the neurotransmitter, adenosine triphosphate (ATP). To validate the proposed structural model of channel synapses, the ultrastructural localization of CALHM1 in type II cells of both fungiform and circumvallate taste buds was examined. A monoclonal antibody against CALHM1 was developed and its localization was evaluated via immunofluorescence and immunoelectron microscopy using the immunogold-silver labeling technique. CALHM1 was detected as puncta using immunofluorescence and along the presynaptic membrane of channel synapses facing atypical mitochondria, which provide ATP, by immunoelectron microscopy. In addition, it was detected along the plasma membrane lined by subsurface cisternae at sites apposed to afferent nerve fibers. Our results support the validity of a previously proposed structural model for channel synapses and provide insights into the function of subsurface cisternae whose function in taste receptor cells is unknown. We also examined the localization of CALHM1 in hybrid synapses of type III cells, which are conventional chemical synapses accompanied by mitochondria similar to atypical mitochondria of channel synapses. CALHM1 was not detected in the six hybrid synapses examined using immunoelectron microscopy. We further performed double immunolabeling for CALHM1 and Bassoon, which is detected as puncta corresponding to conventional vesicular synapses in type III cells. Our observations suggest that at least some, and probably most, hybrid synapses are not accompanied by CALHM1.
味觉感受器细胞在形态学上分为II型和III型。II型细胞形成一种独特的突触类型,称为通道突触,其中钙稳态调节剂1(CALHM1)与CALHM3一起形成电压门控通道,释放神经递质三磷酸腺苷(ATP)。为了验证所提出的通道突触结构模型,研究了CALHM1在菌状和轮廓乳头味蕾II型细胞中的超微结构定位。开发了一种针对CALHM1的单克隆抗体,并使用免疫金银标记技术通过免疫荧光和免疫电子显微镜评估其定位。通过免疫荧光检测到CALHM1为点状,通过免疫电子显微镜在面向提供ATP的非典型线粒体的通道突触的突触前膜上检测到CALHM1。此外,在与传入神经纤维相对的部位,沿着由表面下池衬里的质膜检测到它。我们的结果支持了先前提出的通道突触结构模型的有效性,并为表面下池的功能提供了见解,其在味觉感受器细胞中的功能尚不清楚。我们还研究了CALHM1在III型细胞混合突触中的定位,III型细胞的混合突触是传统的化学突触,伴有类似于通道突触非典型线粒体的线粒体。在使用免疫电子显微镜检查的六个混合突触中未检测到CALHM1。我们进一步对CALHM1和巴松管进行了双重免疫标记,巴松管在III型细胞中被检测为与传统囊泡突触相对应的点状。我们的观察结果表明,至少一些,可能大多数混合突触不伴有CALHM1。