Local Regulators (local + regulator)

Distribution by Scientific Domains


Selected Abstracts


Regulation of uterine function by cytokines in cows: Possible actions of tumor necrosis factor-,, interleukin-1, and interferon-,

ANIMAL SCIENCE JOURNAL, Issue 3 2006
Kiyoshi OKUDA
ABSTRACT When animals do not become pregnant, regression of the corpus luteum (CL) is essential for normal cyclicity because it allows the development of a new ovulatory follicle. Luteal regression is caused by a pulsatile release of prostaglandin (PG) F2, from the uterus in the late luteal phase in most mammals including cattle. Although it has been proposed in ruminants that pulsatile PGF2, secretion is generated by a positive feedback loop between luteal and/or hypophyseal oxytocin and uterine PGF2,, the bovine endometrium may possess other mechanisms for initiation of luteolytic PGF2, secretion. There is increasing evidence that several cytokines mainly produced by immune cells modulate CL and uterine function in many species. Tumor necrosis factor-, (TNF-,) stimulates PGF2, output from bovine endometrium not only at the follicular phase but also at the late luteal phase. Administration of TNF-, at a high concentration prolongs luteal lifespan, whereas administration of a low concentration of TNF-, accelerates luteal regression in cows. The data obtained from the authors' previous in vitro and in vivo studies strongly suggest that TNF-, is a crucial factor in regulating luteolysis in cows. The authors' recent study has shown that interleukin-1, mediates PG secretion from bovine endometrium as a local regulator. Furthermore, interferon-, (IFN-,) suppresses the action of TNF-, on PGF2, synthesis by the bovine endometrium in vitro, suggesting that IFN-, plays a luteoprotective role by inhibiting TNF-,-induced PGF2, production in early pregnancy. The purpose of the present review is to summarize current understanding of the endocrine mechanisms that regulate uterine function by cytokines during the estrous cycle and early pregnancy in cows. [source]


DNA methylation and chromatin accessibility of the proximal Cyp19 promoter region 1.5/2 correlate with expression levels in sheep placentomes

MOLECULAR REPRODUCTION & DEVELOPMENT, Issue 1 2008
Rainer Fürbass
Abstract Placental oestrogens play an important role as local regulators of placental growth and differentiation during gestation, and toward term they are also involved in the preparation of parturition. They are synthesized within the fetal cotyledons of placentomes by aromatase cytochrome P450 (P450arom; EC 1.14.14.1), the product of the Cyp19 gene. The first step of regulation of P450arom expression, and hence enzyme activity and oestrogen production, takes place at the level of Cyp19 transcription, which is driven by a proximal promoter region, P1.5/2, in the sheep placenta. The aim of the present study was to find out if different Cyp19 expression levels, which previously had been observed in ovine placentome tissues, correlate with the tissue-specific chromatin structure of the promoter. To this end, we investigated the chromatin structure across the P1.5/2 region in caruncles and cotyledons from 100 and 125 days pregnant ewes, and in term placentae, respectively, by analyzing the DNA methylation and the accessibility to restriction digestion. Our data show that: (1) cotyledonal DNA was significantly lower methylated than caruncular DNA; (2) methylation of cotyledonal DNA was low at 100 and 125 days of pregnancy, and increased to a significant higher level in term placentae; and (3) concurrently, cotyledonal chromatin became inaccessible to restriction digestion at term of gestation. The results imply that DNA methylation and chromatin accessibility of the P1.5/2 promoter region correlate with expression levels of the Cyp19 gene. Mol. Reprod. Dev. 75: 1,7, 2008. © 2007 Wiley-Liss, Inc. [source]


Immunohistochemical Localization of Oestrogen Receptors , and ,, Progesterone Receptor and Aromatase in the Equine Placenta

REPRODUCTION IN DOMESTIC ANIMALS, Issue 2 2009
MMM Abd-Elnaeim
Contents The functions of placental oestrogens during equine pregnancy are still unclear. Yet, they may act predominantly as local regulators of growth and differentiation in the microplacentomes. Thus, expression patterns of oestrogen receptors (ERs) , and , were investigated in the microcotyledonary placenta from pregnant mares at 110, 121, 179, 199 and 309 days of gestation by immunohistochemistry. In microplacentomes, both the ER isoforms were detected in trophoblast (T) cells, chorionic villous stroma (FS), microcaruncular epithelium (ME) and microcaruncular stroma (MS). Proportions of positive cells were 38,91% (T), 11,41% (FS), 55,89% (ME), 17,51% (MS) for ER, and 66,76% (T), 21,37% (FS), 41,68% (ME) and 24,55% (MS) for ER,. Between days 110 and 199, proportions of cells positive for progesterone receptor (PR) varied between 19% and 62% (T), 3% and 50% (CS), 15% and 46% (ME), and 4% and 33% (MS). At day 309, PR was virtually absent in T, CS and ME (percentages < 0.1), whereas in MS 14.3% of cells were still positive. The expression of ERs and PR in equine microplacentomes gives evidence for a role of placental steroids as regulators of placental growth, differentiation and function. The detection of ER,, ER, and PR in foetal and maternal vascular tissue suggests that placental steroids are also involved in the control of placental angiogenesis and,/or vascular functions. The co-localization of ERs with aromatase in T suggests auto- or intracrine functions of oestrogens in this cell type. [source]


Roles of reactive oxygen species in the corpus luteum

ANIMAL SCIENCE JOURNAL, Issue 6 2006
Norihiro SUGINO
ABSTRACT Cells living under aerobic conditions always face the oxygen paradox. Oxygen is necessary for cells to maintain their lives. However, reactive oxygen species such as superoxide radicals, hydroxyl radicals and hydrogen peroxide are generated from oxygen and damage cells. Oxidative stress occurs as a consequence of the excessive production of reactive oxygen species and impaired antioxidant defense systems. Antioxidant enzymes include superoxide dismutase (SOD), which is a specific enzyme to scavenge superoxide radicals; copper-zinc SOD, located in the cytosol and Mn-SOD, located in the mitochondria. Both types of SOD belong to the first enzymatic step to scavenge superoxide radicals. It has been reported that a number of local factors such as cytokines, growth factors and eicosanoids are involved in the regulation of the corpus luteum (CL) function in addition to gonadotropins. Since reactive oxygen species are generated and SOD is expressed in the CL, there is a possibility that reactive oxygen species and SOD work as local regulators of the CL function. The present review reports that reactive oxygen species and their scavenging systems play important roles in the regulation of the CL function. [source]