Endocrine and local control of the primate corpus luteum
The primate corpus luteum is a transient endocrine gland that differentiates from the ovulatory follicle midway through the ovarian (menstrual) cycle. Its formation and limited lifespan is critical for fertility, as luteal-derived progesterone is the essential steroid hormone required for embryo imp...
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Published in | Reproductive biology Vol. 13; no. 4; pp. 259 - 271 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Poland
Elsevier B.V
01.12.2013
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Subjects | |
Online Access | Get full text |
ISSN | 1642-431X 2300-732X |
DOI | 10.1016/j.repbio.2013.08.002 |
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Abstract | The primate corpus luteum is a transient endocrine gland that differentiates from the ovulatory follicle midway through the ovarian (menstrual) cycle. Its formation and limited lifespan is critical for fertility, as luteal-derived progesterone is the essential steroid hormone required for embryo implantation and maintenance of intra-uterine pregnancy until the placenta develops. It is well-established that LH and the LH-like hormone, CG, are the vital luteotropic hormones during the menstrual cycle and early pregnancy, respectively. Recent advances, particularly through genome analyses and cellular studies, increased our understanding of various local factors and cellular processes associated with the development, maintenance and repression of the corpus luteum. These include paracrine or autocrine factors associated with angiogenesis (e.g., VEGF), and that mediate LH/CG actions (e.g., progesterone), or counteract luteotropic effects (i.e., local luteolysis; e.g., PGF2α). However, areas of mystery and controversy remain, particularly regarding the signals and events that initiate luteal regression in the non-fecund cycle. Novel approaches capable of gene “knockdown” or amplification”, in vivo as well as in vitro, should identify novel or underappreciated gene products that are regulated by or modulate LH/CG actions to control the functional lifespan of the primate corpus luteum. Further advances in our understanding of luteal physiology will help to improve or control fertility for purposes ranging from preservation of endangered primate species to designing novel ovary-based contraceptives and treating ovarian disorders in women. |
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AbstractList | The primate corpus luteum is a transient endocrine gland that differentiates from the ovulatory follicle midway through the ovarian (menstrual) cycle. Its formation and limited lifespan is critical for fertility, as luteal-derived progesterone is the essential steroid hormone required for embryo implantation and maintenance of intra-uterine pregnancy until the placenta develops. It is well-established that LH and the LH-like hormone, CG, are the vital luteotropic hormones during the menstrual cycle and early pregnancy, respectively. Recent advances, particularly through genome analyses and cellular studies, increased our understanding of various local factors and cellular processes associated with the development, maintenance and repression of the corpus luteum. These include paracrine or autocrine factors associated with angiogenesis (e.g., VEGF), and that mediate LH/CG actions (e.g., progesterone), or counteract luteotropic effects (i.e., local luteolysis; e.g., PGF
2α
). However, areas of mystery and controversy remain, particularly regarding the signals and events that initiate luteal regression in the non-fecund cycle. Novel approaches capable of gene “knockdown” or amplification”, in vivo as well as in vitro, should identify novel or underappreciated gene products that are regulated by or modulate LH/CG actions to control the functional lifespan of the primate corpus luteum. Further advances in our understanding of luteal physiology will help to improve or control fertility for purposes ranging from preservation of endangered primate species to designing novel ovary-based contraceptives and treating ovarian disorders in women. R01 HD020869, R01 HD042000, U54 HD018185, U54 HD055744, P51 OD011092, T32 HD007133, Bayer Schering Pharma AG. The primate corpus luteum is a transient endocrine gland that differentiates from the ovulatory follicle midway through the ovarian (menstrual) cycle. Its formation and limited lifespan is critical for fertility, as luteal-derived progesterone is the essential steroid hormone required for embryo implantation and maintenance of intra-uterine pregnancy until the placenta develops. It is well-established that LH and the LH-like hormone, CG, are the vital luteotropic hormones during the menstrual cycle and early pregnancy, respectively. Recent advances, particularly through genome analyses and cellular studies, increased our understanding of various local factors and cellular processes associated with the development, maintenance and repression of the corpus luteum. These include paracrine or autocrine factors associated with angiogenesis (e.g., VEGF), and that mediate LH/CG actions (e.g., progesterone), or counteract luteotropic effects (i.e., local luteolysis; e.g., PGF2α). However, areas of mystery and controversy remain, particularly regarding the signals and events that initiate luteal regression in the non-fecund cycle. Novel approaches capable of gene "knockdown" or amplification", in vivo as well as in vitro, should identify novel or underappreciated gene products that are regulated by or modulate LH/CG actions to control the functional lifespan of the primate corpus luteum. Further advances in our understanding of luteal physiology will help to improve or control fertility for purposes ranging from preservation of endangered primate species to designing novel ovary-based contraceptives and treating ovarian disorders in women. Abstract The primate corpus luteum is a transient endocrine gland that differentiates from the ovulatory follicle midway through the ovarian (menstrual) cycle. Its formation and limited lifespan is critical for fertility, as luteal-derived progesterone is the essential steroid hormone required for embryo implantation and maintenance of intra-uterine pregnancy until the placenta develops. It is well-established that LH and the LH-like hormone, CG, are the vital luteotropic hormones during the menstrual cycle and early pregnancy, respectively. Recent advances, particularly through genome analyses and cellular studies, increased our understanding of various local factors and cellular processes associated with the development, maintenance and repression of the corpus luteum. These include paracrine or autocrine factors associated with angiogenesis (e.g., VEGF), and that mediate LH/CG actions (e.g., progesterone), or counteract luteotropic effects (i.e., local luteolysis; e.g., PGF2α ). However, areas of mystery and controversy remain, particularly regarding the signals and events that initiate luteal regression in the non-fecund cycle. Novel approaches capable of gene “knockdown” or amplification”, in vivo as well as in vitro, should identify novel or underappreciated gene products that are regulated by or modulate LH/CG actions to control the functional lifespan of the primate corpus luteum. Further advances in our understanding of luteal physiology will help to improve or control fertility for purposes ranging from preservation of endangered primate species to designing novel ovary-based contraceptives and treating ovarian disorders in women. |
Author | Hennebold, Jon D. Stouffer, Richard L. Xu, Fuhua Bogan, Randy L. Bishop, Cecily V. |
Author_xml | – sequence: 1 givenname: Richard L. surname: Stouffer fullname: Stouffer, Richard L. email: stouffri@ohsu.edu organization: Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Beaverton, OR, USA – sequence: 2 givenname: Cecily V. surname: Bishop fullname: Bishop, Cecily V. organization: Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Beaverton, OR, USA – sequence: 3 givenname: Randy L. surname: Bogan fullname: Bogan, Randy L. organization: Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Beaverton, OR, USA – sequence: 4 givenname: Fuhua surname: Xu fullname: Xu, Fuhua organization: Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Beaverton, OR, USA – sequence: 5 givenname: Jon D. surname: Hennebold fullname: Hennebold, Jon D. organization: Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Beaverton, OR, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24287034$$D View this record in MEDLINE/PubMed |
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Keywords | LH–CG Luteinization Luteolytic factors Luteolysis Luteotropic factors |
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Snippet | The primate corpus luteum is a transient endocrine gland that differentiates from the ovulatory follicle midway through the ovarian (menstrual) cycle. Its... Abstract The primate corpus luteum is a transient endocrine gland that differentiates from the ovulatory follicle midway through the ovarian (menstrual) cycle.... |
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StartPage | 259 |
SubjectTerms | Animals Chorionic Gonadotropin - metabolism Corpus Luteum - blood supply Corpus Luteum - growth & development Corpus Luteum - metabolism Female Fertility - physiology Humans Kisspeptins - metabolism LH–CG Luteinization Luteinizing Hormone - metabolism Luteolysis Luteolysis - physiology Luteolytic factors Luteotropic factors Neovascularization, Physiologic - physiology Obstetrics and Gynecology Pregnancy Primates - metabolism Primates - physiology Progesterone - metabolism |
Title | Endocrine and local control of the primate corpus luteum |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S1642431X1300274X https://www.clinicalkey.es/playcontent/1-s2.0-S1642431X1300274X https://dx.doi.org/10.1016/j.repbio.2013.08.002 https://www.ncbi.nlm.nih.gov/pubmed/24287034 https://pubmed.ncbi.nlm.nih.gov/PMC4001828 |
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