BDNF-TrkB signaling in oxytocin neurons contributes to maternal behavior

Kristen R. Maynard, John W. Hobbs, Badoi N. Phan, Amolika Gupta, Sumita Rajpurohit, Courtney Williams, Anandita Rajpurohit, Joo Heon Shin, Andrew E. Jaffe, Keri Martinowich

Research output: Contribution to journalArticlepeer-review

10 Scopus citations


Brain-derived neurotrophic factor (Bdnf) transcription is controlled by several promoters, which drive expression of multiple transcripts encoding an identical protein. We previously reported that BDNF derived from promoters I and II is highly expressed in hypothalamus and is critical for regulating aggression in male mice. Here we report that BDNF loss from these promoters causes reduced sexual receptivity and impaired maternal care in female mice, which is concomitant with decreased oxytocin (Oxt) expression during development. We identify a novel link between BDNF signaling, oxytocin, and maternal behavior by demonstrating that ablation of TrkB selectively in OXT neurons partially recapitulates maternal care impairments observed in BDNF-deficient females. Using translating ribosome affinity purification and RNA-sequencing we define a molecular profile for OXT neurons and delineate how BDNF signaling impacts gene pathways critical for structural and functional plasticity. Our findings highlight BDNF as a modulator of sexually-dimorphic hypothalamic circuits that govern female-typical behaviors.

Original languageEnglish (US)
Article numbere33676
StatePublished - Sep 2018

ASJC Scopus subject areas

  • General Neuroscience
  • General Immunology and Microbiology
  • General Biochemistry, Genetics and Molecular Biology


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