Involvement of membrane palmitoylated protein 2 (MPP2) in the synaptic molecular complex at the mouse cerebellar glomerulus

• Published in: Histochemistry and cell biology Vol. 158; no. 5; pp. 497 - 511
• Main Authors: Yamada, Tomoki, Saitoh, Yurika, Kametani, Kiyokazu, Kamijo, Akio, Sakamoto, Takeharu, Terada, Nobuo
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.11.2022; Springer Nature B.V
• Subjects: Adherens junctions; Biochemistry; Biomedical and Life Sciences; Biomedicine; Cadherins; Calcium-binding protein; Calmodulin; Cell adhesion molecules; Cell Biology; Cell membranes; Central nervous system; Cerebellum; Developmental Biology; Glomerulus; Glutamic acid receptors; Glutamic acid receptors (ionotropic); Granule cells; Immunoprecipitation; Kinases; Localization; Membrane proteins; Mossy fibers; Myelin; N-Methyl-D-aspartic acid receptors; Nervous system; Original Paper; Protein kinase; Protein transport; Proteins; Schwann cells; Cerebellum; MPP2; Lin7; Membrane skeletal protein; Cerebellar glomerulus
• DOI: 10.1007/s00418-022-02137-6
• ISSN: 0948-6143; 1432-119X

We previously reported that the membrane skeletal protein 4.1G in the peripheral nervous system transports membrane palmitoylated protein 6 (MPP6), which interacts with the synaptic scaffolding protein Lin7 and cell adhesion molecule 4 (CADM4) in Schwann cells that form myelin. In the present study, we investigated the localization of and proteins related to MPP2, a highly homologous family protein of MPP6, in the cerebellum of the mouse central nervous system, in which neurons are well organized. Immunostaining for MPP2 was observed at cerebellar glomeruli (CG) in the granular layer after postnatal day 14. Using the high-resolution Airyscan mode of a confocal laser-scanning microscope, MPP2 was detected as a dot pattern and colocalized with CADM1 and Lin7, recognized as small ring/line patterns, as well as with calcium/calmodulin-dependent serine protein kinase (CASK), NMDA glutamate receptor 1 (GluN1), and M-cadherin, recognized as dot patterns, indicating the localization of MPP2 in the excitatory postsynaptic region and adherens junctions of granule cells. An immunoprecipitation analysis revealed that MPP2 formed a molecular complex with CADM1, CASK, M-cadherin, and Lin7. Furthermore, the Lin7 staining pattern showed small rings surrounding mossy fibers in wild-type CG, while it changed to the dot/spot pattern inside small rings detected with CADM1 staining in MPP2-deficient CG. These results indicate that MPP2 influences the distribution of Lin7 to synaptic cell membranes at postsynaptic regions in granule cells at CG, at which electric signals enter the cerebellum.