1.Animal Models for the Study of Polycystic Ovarian Syndrome.
Oliver OAKLEY ; Po Ching LIN ; Phillip BRIDGES ; CheMyong KO
Endocrinology and Metabolism 2011;26(3):193-202
No abstract available.
Animals
;
Models, Animal
;
Polycystic Ovary Syndrome
2.Lifetime changes of the oocyte pool: Contributing factors with a focus on ovulatory inflammation
Chan Jin PARK ; Ji-Eun OH ; Jianan FENG ; Yoon Min CHO ; Huanyu QIAO ; CheMyong KO
Clinical and Experimental Reproductive Medicine 2022;49(1):16-25
In mammalian species, females are born with a number of oocytes exceeding what they release via ovulation. In humans, an average girl is born with over a thousand times more oocytes than she will ovulate in her lifetime. The reason for having such an excessive number of oocytes in a neonatal female ovary is currently unknown. However, it is well established that the oocyte number decreases throughout the entire lifetime until the ovary loses them all. In this review, data published in the past 80 years were used to assess the current knowledge regarding the changing number of oocytes in humans and mice, as well as the reported factors that contribute to the decline of oocyte numbers. Briefly, a collective estimation indicates that an average girl is born with approximately 600,000 oocytes, which is 2,000 times more than the number of oocytes that she will ovulate in her lifetime. The oocyte number begins to decrease immediately after birth and is reduced to half of the initial number by puberty and almost zero by age 50 years. Multiple factors that are either intrinsic or extrinsic to the ovary contribute to the decline of the oocyte number. The inflammation caused by the ovulatory luteinizing hormone surge is discussed as a potential contributing factor to the decline of the oocyte pool during the reproductive lifespan.
3.Porcine intestinal lymphoid tissues synthesize estradiol
Chan Jin PARK ; Heehyen KIM ; Jooyoung JIN ; Radwa BARAKAT ; Po Ching LIN ; Jeong Moon CHOI ; CheMyong Jay KO
Journal of Veterinary Science 2018;19(4):477-482
Estradiol (17β-estradiol) is synthesized primarily in the gonads of both sexes and regulates the development and function of reproductive organs. Recently, we reported that intestinal lymphocyte homeostasis is regulated by estradiol synthesized de novo in the endothelial cells of the high endothelial venules (HEVs) of mesenteric lymph nodes and Peyer's patches in mice. This observation prompted us to hypothesize that HEVs of intestinal lymphoid tissues are sites of estradiol synthesis across species. In this study, we examined whether estradiol is synthesized in the intestinal lymphoid tissues of adolescent piglets. Comparisons of estradiol levels in blood and tissue showed that estradiol concentrations in mesenteric lymph nodes and Peyer's patches were significantly higher than the level in serum. Reverse transcription polymerase chain reaction showed that porcine intestinal lymphoid tissues express mRNAs for steroidogenic enzymes (StAR, 17β-Hsd, 3β-Hsd, Cyp17a1, and Cyp19a1), and immunohistochemical results in ilial tissue showed expression of aromatase (CYP19) in Peyer's patch-localized endothelial cells of HEVs. When mesenteric lymph node and Peyer's patch tissues were cultured in vitro, they produced estradiol. Taken together, the results indicate that mesenteric lymph nodes and Peyer's patches are sites of estradiol synthesis in adolescent piglets.
Adolescent
;
Animals
;
Aromatase
;
Endothelial Cells
;
Estradiol
;
Gonads
;
Homeostasis
;
Humans
;
In Vitro Techniques
;
Intestines
;
Lymph Nodes
;
Lymphocytes
;
Lymphoid Tissue
;
Mice
;
Peyer's Patches
;
Polymerase Chain Reaction
;
Reverse Transcription
;
RNA, Messenger
;
Swine
;
Venules