| First Author | Liakath-Ali K | Year | 2022 |
| Journal | Proc Natl Acad Sci U S A | Volume | 119 |
| Issue | 20 | Pages | e2123421119 |
| PubMed ID | 35544694 | Mgi Jnum | J:331253 |
| Mgi Id | MGI:7386700 | Doi | 10.1073/pnas.2123421119 |
| Citation | Liakath-Ali K, et al. (2022) Transsynaptic cerebellin 4-neogenin 1 signaling mediates LTP in the mouse dentate gyrus. Proc Natl Acad Sci U S A 119(20):e2123421119 |
| abstractText | Five decades ago, long-term potentiation (LTP) of synaptic transmission was discovered at entorhinal cortex-->dentate gyrus (EC-->DG) synapses, but the molecular determinants of EC-->DG LTP remain largely unknown. Here, we show that the presynaptic neurexin-ligand cerebellin-4 (Cbln4) is highly expressed in the entorhinal cortex and essential for LTP at EC-->DG synapses, but dispensable for basal synaptic transmission at these synapses. Cbln4, when bound to cell-surface neurexins, forms transcellular complexes by interacting with postsynaptic DCC (deleted in colorectal cancer) or neogenin-1. DCC and neogenin-1 act as netrin and repulsive guidance molecule-a (RGMa) receptors that mediate axon guidance in the developing brain, but their binding to Cbln4 raised the possibility that they might additionally function in the mature brain as postsynaptic receptors for presynaptic neurexin/Cbln4 complexes, and that as such receptors, DCC or neogenin-1 might mediate EC-->DG LTP that depends on Cbln4. Indeed, we observed that neogenin-1, but not DCC, is abundantly expressed in dentate gyrus granule cells, and that postsynaptic neogenin-1 deletions in dentate granule cells blocked EC-->DG LTP, but again did not affect basal synaptic transmission similar to the presynaptic Cbln4 deletions. Thus, binding of presynaptic Cbln4 to postsynaptic neogenin-1 renders EC-->DG synapses competent for LTP, but is not required for establishing these synapses or for otherwise enabling their function. |
