TY - JOUR
T1 - Nonhuman primates
T2 - A vital model for basic and applied research on female reproduction, prenatal development, and women's health
AU - Stouffer, Richard L.
AU - Woodruff, Teresa K.
N1 - Funding Information:
Special thanks to scientists that contributed to the NIH presentation, Drs. Charles Roberts (Oregon National Primate Research Center), Jon Levine and David Abbott (Wisconsin National Primate Research Center), Kyle Orwig (University of Pittsburgh), and Asgi Fazeleabas (Michigan State University). The authors' research is funded primarily through the NIH, especially the Eunice Kennedy Shriver National Institute of Child Health and Human Development, including the National Centers for Translational Research in Reproduction and Infertility (P50 HD076188, TKW; P50 HD071836, RLS) and Contraceptive Development and Research Center (U54 HD055744, RLS). Dr. Stouffer's research is supported by the resources and infrastructure of the NIH Primate Centers program, Office of the Director (P51 OD011092).
Funding Information:
Special thanks to scientists that contributed to the NIH presentation, Drs. Charles Roberts (Oregon National Primate Research Center), Jon Levine and David Abbott (Wisconsin National Primate Research Center), Kyle Orwig (University of Pittsburgh), and Asgi Fazeleabas (Michigan State University). The authors’ research is funded primarily through the NIH, especially the Eunice Kennedy Shriver National Institute of Child Health and Human Development, including the National Centers for Translational Research in Reproduction and Infertility (P50 HD076188, TKW; P50 HD071836, RLS) and Contraceptive Development and Research Center (U54 HD055744, RLS). Dr. Stouffer’s research is supported by the resources and infrastructure of the NIH Primate Centers program, Office of the Director (P51 OD011092).
Publisher Copyright:
© The Author(s) 2017. Published by Oxford University Press on behalf of the National Academy of Sciences. All rights reserved.
PY - 2017/12/1
Y1 - 2017/12/1
N2 - The comparative biology of reproduction and development in mammalian species is remarkable. Hence, because of similarities in environmental and neuroendocrine control of the reproductive axis, the cyclic function of the ovary and reproductive tract, establishment and control of the maternal-fetal-placental unit during pregnancy, and reproductive aging from puberty through menopause, nonhuman primates (NHPs) are valuable models for research related to women's reproductive health and its disorders. This chapter provides examples of research over the past 10+ years using Old World monkeys (notably macaque species), baboons, and to a lesser extent New World monkeys (especially marmosets) that contributed to our understanding of the etiology and therapies or prevention of: (1) ovarian disorders, e.g., polycystic ovary syndrome, mitochondrial DNA-based diseases from the oocyte; (2) uterine disorders, for example, endometriosis and uterine transplantation; and (3) pregnancy disorders, for example, preterm labor and delivery, environmental factors. Also, emerging opportunities such as viral (e.g., Zika) induced fetal defects and germline genomic editing to generate valuable primate models of human diseases (e.g., Huntington and muscular dystrophy) are addressed. Although the high costs, specialized resources, and ethical debate challenge the use of primates in biomedical research, their inclusion in fertility and infertility research is vital for continued improvements in women's reproductive health.
AB - The comparative biology of reproduction and development in mammalian species is remarkable. Hence, because of similarities in environmental and neuroendocrine control of the reproductive axis, the cyclic function of the ovary and reproductive tract, establishment and control of the maternal-fetal-placental unit during pregnancy, and reproductive aging from puberty through menopause, nonhuman primates (NHPs) are valuable models for research related to women's reproductive health and its disorders. This chapter provides examples of research over the past 10+ years using Old World monkeys (notably macaque species), baboons, and to a lesser extent New World monkeys (especially marmosets) that contributed to our understanding of the etiology and therapies or prevention of: (1) ovarian disorders, e.g., polycystic ovary syndrome, mitochondrial DNA-based diseases from the oocyte; (2) uterine disorders, for example, endometriosis and uterine transplantation; and (3) pregnancy disorders, for example, preterm labor and delivery, environmental factors. Also, emerging opportunities such as viral (e.g., Zika) induced fetal defects and germline genomic editing to generate valuable primate models of human diseases (e.g., Huntington and muscular dystrophy) are addressed. Although the high costs, specialized resources, and ethical debate challenge the use of primates in biomedical research, their inclusion in fertility and infertility research is vital for continued improvements in women's reproductive health.
KW - Contraception
KW - Endometriosis
KW - Germline genome editing
KW - Infertility
KW - Mitochondrial DNA-based diseases
KW - Polycystic ovary syndrome
KW - Preterm labor and delivery
KW - Uterine transplantation
KW - Zika virus-induced fetal defects
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U2 - 10.1093/ilar/ilx027
DO - 10.1093/ilar/ilx027
M3 - Article
C2 - 28985318
AN - SCOPUS:85040788885
SN - 1084-2020
VL - 58
SP - 281
EP - 294
JO - ILAR Journal
JF - ILAR Journal
IS - 2
ER -