The scheduling of adolescence with Netrin-1 and UNC5C

Author:

Hoops Daniel12ORCID,Kyne Robert3,Salameh Samer24,MacGowan Del24,Avramescu Radu Gabriel12,Ewing Elise24,He Alina Tao24,Orsini Taylor24,Durand Anais24ORCID,Popescu Christina24,Zhao Janet Mengyi24,Shatz Kelcie5,Li LiPing5,Carroll Quinn5,Liu Guofa6,Paul Matthew J35ORCID,Flores Cecilia1278ORCID

Affiliation:

1. Department of Psychiatry, McGill University

2. Douglas Mental Health University Institute

3. Neuroscience Program, University at Buffalo

4. Integrated Program in Neuroscience, McGill University

5. Department of Psychology, University at Buffalo

6. Department of Biological Sciences, University of Toledo

7. Department of Neurology and Neurosurgery, McGill University

8. Ludmer Centre for Neuroinformatics & Mental Health, McGill University

Abstract

Dopamine axons are the only axons known to grow during adolescence. Here, using rodent models, we examined how two proteins, Netrin-1 and its receptor, UNC5C, guide dopamine axons toward the prefrontal cortex and shape behaviour. We demonstrate in mice (Mus musculus) that dopamine axons reach the cortex through a transient gradient of Netrin-1-expressing cells – disrupting this gradient reroutes axons away from their target. Using a seasonal model (Siberian hamsters; Phodopus sungorus) we find that mesocortical dopamine development can be regulated by a natural environmental cue (daylength) in a sexually dimorphic manner – delayed in males, but advanced in females. The timings of dopamine axon growth and UNC5C expression are always phase-locked. Adolescence is an ill-defined, transitional period; we pinpoint neurodevelopmental markers underlying this period.

Funder

National Institute on Drug Abuse

Canadian Institutes of Health Research

National Science and Engineering Research Council of Canada

National Science Foundation

Publisher

eLife Sciences Publications, Ltd

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