| First Author | Gingrich EC | Year | 2026 |
| Journal | Curr Biol | Volume | 36 |
| Issue | 10 | Pages | 2622-2636.e5 |
| PubMed ID | 42105755 | Mgi Jnum | J:385796 |
| Mgi Id | MGI:8344107 | Doi | 10.1016/j.cub.2026.04.038 |
| Citation | Gingrich EC, et al. (2026) Ten3-Lphn2-mediated target selection across the extended hippocampal network demonstrates a repeated strategy for circuit assembly. Curr Biol |
| abstractText | How do thousands of cell-surface proteins specify billions of neuronal connections in developing brains? We previously found that inverse expression of a ligand-receptor pair, teneurin-3 (Ten3) and latrophilin-2 (Lphn2), in CA1 and subiculum, instructs CA1-->subiculum target selection through Ten3-Ten3 homophilic attraction and Ten3-Lphn2 heterophilic reciprocal repulsions. Here, we leveraged conditional knockouts to demonstrate that these mechanisms generalize to several nodes of the extended hippocampal networks, including entorhinal cortex and hypothalamus. Cooperation between attraction and repulsion may differ depending on the order in which developing axons encounter the attractant and repellent subfields. Ten3 and Lphn2 can serve as both ligands for incoming axons and as receptors for their own target selection within the same neuron; Ten3 can be repulsive or attractive as a ligand or receptor. Thus, multifunctionality and repeated use, together with recurrent circuit motifs prevalent in the brain, enable one ligand-receptor pair to instruct target selection of many neurons. |
