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Alternatively spliced mini-exon B in PTPδ regulates excitatory synapses through cell-type-specific trans-synaptic PTPδ-IL1RAP interaction

Author

Listed:
  • Seoyeong Kim

    (Korea Advanced Institute for Science and Technology (KAIST)
    Institute for Basic Science (IBS))

  • Jae Jin Shin

    (Institute for Basic Science (IBS))

  • Muwon Kang

    (Korea Advanced Institute for Science and Technology (KAIST)
    Institute for Basic Science (IBS))

  • Yeji Yang

    (Korea Advanced Institute for Science and Technology (KAIST)
    Korea Basic Science Institute (KBSI))

  • Yi Sul Cho

    (Kyungpook National University)

  • Hyojung Paik

    (Korea Institute of Science and Technology Information (KISTI))

  • Jimin Kim

    (Korea Institute of Science and Technology Information (KISTI))

  • Yunho Yi

    (Korea Advanced Institute for Science and Technology (KAIST))

  • Suho Lee

    (Institute for Basic Science (IBS))

  • Hei Yeun Koo

    (Yonsei University College of Medicine)

  • Jinwoong Bok

    (Yonsei University College of Medicine)

  • Yong Chul Bae

    (Kyungpook National University)

  • Jin Young Kim

    (Korea Basic Science Institute (KBSI))

  • Eunjoon Kim

    (Korea Advanced Institute for Science and Technology (KAIST)
    Institute for Basic Science (IBS))

Abstract

PTPδ, encoded by PTPRD, is implicated in various neurological, psychiatric, and neurodevelopmental disorders, but the underlying mechanisms remain unclear. PTPδ trans-synaptically interacts with multiple postsynaptic adhesion molecules, which involves its extracellular alternatively spliced mini-exons, meA and meB. While PTPδ-meA functions have been studied in vivo, PTPδ-meB has not been studied. Here, we report that, unlike homozygous PTPδ-meA-mutant mice, homozygous PTPδ-meB-mutant (Ptprd-meB–/–) mice show markedly reduced early postnatal survival. Heterozygous Ptprd-meB+/– male mice show behavioral abnormalities and decreased excitatory synaptic density and transmission in dentate gyrus granule cells (DG-GCs). Proteomic analyses identify decreased postsynaptic density levels of IL1RAP, a known trans-synaptic partner of meB-containing PTPδ. Accordingly, IL1RAP-mutant mice show decreased excitatory synaptic transmission in DG-GCs. Ptprd-meB+/– DG interneurons with minimal IL1RAP expression show increased excitatory synaptic density and transmission. Therefore, PTPδ-meB is important for survival, synaptic, and behavioral phenotypes and regulates excitatory synapses in cell-type-specific and IL1RAP-dependent manners.

Suggested Citation

  • Seoyeong Kim & Jae Jin Shin & Muwon Kang & Yeji Yang & Yi Sul Cho & Hyojung Paik & Jimin Kim & Yunho Yi & Suho Lee & Hei Yeun Koo & Jinwoong Bok & Yong Chul Bae & Jin Young Kim & Eunjoon Kim, 2025. "Alternatively spliced mini-exon B in PTPδ regulates excitatory synapses through cell-type-specific trans-synaptic PTPδ-IL1RAP interaction," Nature Communications, Nature, vol. 16(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59685-3
    DOI: 10.1038/s41467-025-59685-3
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    1. Charlotte H. Coles & Nikolaos Mitakidis & Peng Zhang & Jonathan Elegheert & Weixian Lu & Andrew W. Stoker & Terunaga Nakagawa & Ann Marie Craig & E. Yvonne Jones & A. Radu Aricescu, 2014. "Structural basis for extracellular cis and trans RPTPσ signal competition in synaptogenesis," Nature Communications, Nature, vol. 5(1), pages 1-12, December.
    2. Atsushi Yamagata & Tomoyuki Yoshida & Yusuke Sato & Sakurako Goto-Ito & Takeshi Uemura & Asami Maeda & Tomoko Shiroshima & Shiho Iwasawa-Okamoto & Hisashi Mori & Masayoshi Mishina & Shuya Fukai, 2015. "Mechanisms of splicing-dependent trans-synaptic adhesion by PTPδ–IL1RAPL1/IL-1RAcP for synaptic differentiation," Nature Communications, Nature, vol. 6(1), pages 1-11, November.
    3. Claudia Espinoza & Segundo Jose Guzman & Xiaomin Zhang & Peter Jonas, 2018. "Parvalbumin+ interneurons obey unique connectivity rules and establish a powerful lateral-inhibition microcircuit in dentate gyrus," Nature Communications, Nature, vol. 9(1), pages 1-10, December.
    4. Tomoyuki Yoshida & Atsushi Yamagata & Ayako Imai & Juhyon Kim & Hironori Izumi & Shogo Nakashima & Tomoko Shiroshima & Asami Maeda & Shiho Iwasawa-Okamoto & Kenji Azechi & Fumina Osaka & Takashi Saito, 2021. "Canonical versus non-canonical transsynaptic signaling of neuroligin 3 tunes development of sociality in mice," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
    5. Shuai Wang & Chelsea DeLeon & Wenfei Sun & Stephen R. Quake & Bryan L. Roth & Thomas C. Südhof, 2024. "Alternative splicing of latrophilin-3 controls synapse formation," Nature, Nature, vol. 626(7997), pages 128-135, February.
    6. Wenqiang Li & Rui Chen & Laipeng Feng & Xinglun Dang & Jiewei Liu & Tengfei Chen & Jinfeng Yang & Xi Su & Luxian Lv & Tao Li & Zhijun Zhang & Xiong-Jian Luo, 2024. "Genome-wide meta-analysis, functional genomics and integrative analyses implicate new risk genes and therapeutic targets for anxiety disorders," Nature Human Behaviour, Nature, vol. 8(2), pages 361-379, February.
    7. Ji Won Um & Kee Hun Kim & Beom Seok Park & Yeonsoo Choi & Doyoun Kim & Cha Yeon Kim & Soo Jin Kim & Minhye Kim & Ji Seung Ko & Seong-Gyu Lee & Gayoung Choii & Jungyong Nam & Won Do Heo & Eunjoon Kim &, 2014. "Structural basis for LAR-RPTP/Slitrk complex-mediated synaptic adhesion," Nature Communications, Nature, vol. 5(1), pages 1-16, December.
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