Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published April 9, 2019 | Supplemental Material + Submitted + Published
Journal Article Open

Connectional architecture of a mouse hypothalamic circuit node controlling social behavior


Type 1 estrogen receptor-expressing neurons in the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl^(Esr1)) play a causal role in the control of social behaviors, including aggression. Here we use six different viral-genetic tracing methods to systematically map the connectional architecture of VMHvl^(Esr1) neurons. These data reveal a high level of input convergence and output divergence ("fan-in/fan-out") from and to over 30 distinct brain regions, with a high degree (∼90%) of bidirectionality, including both direct as well as indirect feedback. Unbiased collateralization mapping experiments indicate that VMHvl^(Esr1) neurons project to multiple targets. However, we identify two anatomically distinct subpopulations with anterior vs. posterior biases in their collateralization targets. Nevertheless, these two subpopulations receive indistinguishable inputs. These studies suggest an overall system architecture in which an anatomically feed-forward sensory-to-motor processing stream is integrated with a dense, highly recurrent central processing circuit. This architecture differs from the "brain-inspired," hierarchical feed-forward circuits used in certain types of artificial intelligence networks.

Additional Information

© 2019 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND). Contributed by David J. Anderson, December 12, 2018 (sent for review October 11, 2018; reviewed by Clifford B. Saper and Richard B. Simerly). PNAS published ahead of print March 21, 2019. We thank Dr. Miquel Chillón Rodriguez, Dr. Fan Wang, Dr. Liqun Luo, and Dr. Rachael Neve for providing CAV-cre, retrograde Lenti-cre, TRIO reagents, and retrograde HSV-fDIO-cre viruses, respectively, for pilot experiments; Dr. Lynn Enquist and the Center for Neuroanatomy with Neurotropic Viruses viral core center (Princeton University) for H129 recombinants; Dr. Kimberly Ritola of Janelia Research Campus for G-deleted EnvA rabies viruses; Bin Yang for help with cell-volume measurement software; Ben Ouellette for technical help; C. Chiu for laboratory management; and G. Mancuso for administrative assistance. This work was supported by NIH Grants MH070053, MH085082, and MH112593 (to D.J.A.). B.W. is a Howard Hughes Medical Institute Fellow of the Life Sciences Research Foundation. D.J.A. is an Investigator of the Howard Hughes Medical Institute. Author contributions: L.L., D.-W.K., D.J.A., and B.W. designed research; L.L. and D.-W.K. performed research; S.Y., A.C., J.H., and H.Z. contributed new reagents/analytic tools; L.L., D.-W.K., D.J.A., and B.W. analyzed data; and L.L., D.J.A., and B.W. wrote the paper. Reviewers: C.B.S., Harvard Medical School, Beth Israel Deaconess Medical Center; and R.B.S., Vanderbilt University. The authors declare no conflict of interest. This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1817503116/-/DCSupplemental.

Attached Files

Published - 7503.full.pdf

Submitted - 445312.full.pdf

Supplemental Material - pnas.1817503116.sapp.pdf


Files (36.8 MB)
Name Size Download all
8.3 MB Preview Download
26.1 MB Preview Download
2.3 MB Preview Download

Additional details

August 22, 2023
October 23, 2023