TY - JOUR
T1 - Neural crest-derived neurons invade the ovary but not the testis during mouse gonad development
AU - McKey, Jennifer
AU - Bunce, Corey
AU - Batchvarov, Iordan S.
AU - Ornitz, David M.
AU - Capel, Blanche
N1 - Funding Information:
We thank Debra Silver from Duke University for providing us with the Dcx-DsRed mouse line. We also thank Vanda Lennon from Mayo Clinic for the HuC/D antibody. We are grateful to all members of the B.C. laboratory for helpful discussions and suggestions on the project. We would like to acknowledge Danielle Maatouk, who was the first to observe the sexual dimorphism in gonad innervation. This work was supported by a grant from the National Institutes of Health (Grant 1R01HD090050-0) (to B.C.). J.M. was supported by postdoctoral fellowships from the Fondation ARC pour la Recherche contre le Cancer (Award #SAE20151203560) and from the American Cancer Society (Award #130426-PF-17-209-01-TBG). C.B. was supported by a grant from the National Institutes of Health (Grant R37HD039963). Light sheet microscopy was supported by a grant from the National Institutes of Health (Grant 1S10OD020010-01A1) to the Duke Light Microscopy Core Facility and by a voucher from the Duke University School of Medicine.
Funding Information:
ACKNOWLEDGMENTS. We thank Debra Silver from Duke University for providing us with the Dcx-DsRed mouse line. We also thank Vanda Lennon from Mayo Clinic for the HuC/D antibody. We are grateful to all members of the B.C. laboratory for helpful discussions and suggestions on the project. We would like to acknowledge Danielle Maatouk, who was the first to observe the sexual dimorphism in gonad innervation. This work was supported by a grant from the National Institutes of Health (Grant 1R01HD090050-0) (to B.C.). J.M. was supported by postdoctoral fellowships from the Fondation ARC pour la Recherche contre le Cancer (Award #SAE20151203560) and from the American Cancer Society (Award #130426-PF-17-209-01-TBG). C.B. was supported by a grant from the National Institutes of Health (Grant R37HD039963). Light sheet microscopy was supported by a grant from the National Institutes of Health (Grant 1S10OD020010-01A1) to the Duke Light Microscopy Core Facility and by a voucher from the Duke University School of Medicine.
Publisher Copyright:
© 2019 National Academy of Sciences. All Rights Reserved.
PY - 2019
Y1 - 2019
N2 - Testes and ovaries undergo sex-specific morphogenetic changes and adopt strikingly different morphologies, despite the fact that both arise from a common precursor, the bipotential gonad. Previous studies showed that recruitment of vasculature is critical for testis patterning. However, vasculature is not recruited into the early ovary. Peripheral innervation is involved in patterning development of many organs but has been given little attention in gonad development. In this study, we show that while innervation in the male reproductive complex is restricted to the epididymis and vas deferens and never invades the interior of the testis, neural crest-derived innervation invades the interior of the ovary around E16.5. Individual neural crest cells colonize the ovary, differentiate into neurons and glia, and form a dense neural network within the ovarian medulla. Using a sex-reversing mutant mouse line, we show that innervation is specific to ovary development, is not dependent on the genetic sex of gonadal or neural crest cells, and may be blocked by repressive guidance signals elevated in the male pathway. This study reveals another aspect of sexually dimorphic gonad development, establishes a precise timeline and structure of ovarian innervation, and raises many questions for future research.
AB - Testes and ovaries undergo sex-specific morphogenetic changes and adopt strikingly different morphologies, despite the fact that both arise from a common precursor, the bipotential gonad. Previous studies showed that recruitment of vasculature is critical for testis patterning. However, vasculature is not recruited into the early ovary. Peripheral innervation is involved in patterning development of many organs but has been given little attention in gonad development. In this study, we show that while innervation in the male reproductive complex is restricted to the epididymis and vas deferens and never invades the interior of the testis, neural crest-derived innervation invades the interior of the ovary around E16.5. Individual neural crest cells colonize the ovary, differentiate into neurons and glia, and form a dense neural network within the ovarian medulla. Using a sex-reversing mutant mouse line, we show that innervation is specific to ovary development, is not dependent on the genetic sex of gonadal or neural crest cells, and may be blocked by repressive guidance signals elevated in the male pathway. This study reveals another aspect of sexually dimorphic gonad development, establishes a precise timeline and structure of ovarian innervation, and raises many questions for future research.
KW - Innervation
KW - Neural crest
KW - Organogenesis
KW - Ovary
KW - Testis
UR - http://www.scopus.com/inward/record.url?scp=85063256161&partnerID=8YFLogxK
U2 - 10.1073/pnas.1814930116
DO - 10.1073/pnas.1814930116
M3 - Article
C2 - 30819894
AN - SCOPUS:85063256161
SN - 0027-8424
VL - 116
SP - 5570
EP - 5575
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 12
ER -