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1.
Horm Behav ; 88: 15-24, 2017 02.
Artigo em Inglês | MEDLINE | ID: mdl-27760301

RESUMO

Clinical and experimental evidence shows that estrogens affect immunity in mammals. Less is known about this interaction in the evolutionary older, non-mammalian, vertebrates. Fish form an excellent model to identify evolutionary conserved neuroendocrine-immune interactions: i) they are the earliest vertebrates with fully developed innate and adaptive immunity, ii) immune and endocrine parameters vary with season, and iii) physiology is constantly disrupted by increasing contamination of the aquatic environment. Neuro-immuno-endocrine interactions enable adaption to changing internal and external environment and are based on shared signaling molecules and receptors. The presence of specific estrogen receptors on/in fish leukocytes, implies direct estrogen-mediated immunoregulation. Fish leukocytes most probably are also capable to produce estrogens as they express the cyp19a and cyp19b - genes, encoding aromatase cytochrome P450, the enzyme critical for conversion of C19 steroids to estrogens. Immunoregulatory actions of estrogens, vary among animal species, and also with dose, target cell type, or physiological condition (e.g., infected/non-infected, reproductive status). They moreover are multifaceted. Interestingly, season-dependent changes in immune status correlate with changes in the levels of circulating sex hormones. Whereas E2 circulating in the bloodstream is perhaps the most likely candidate to be the physiological mediator of systemic immune-reproductive trade-offs, leukocyte-derived hormones are hypothesized to be mainly involved in local tuning of the immune response. Contamination of the aquatic environment with estrogenic EDCs may violate the delicate and precise allostatic interactions between the endogenous estrogen system and the immune system. This has negative effects on fish health, but will also affect the physiology of its consumers.


Assuntos
Adaptação Fisiológica/fisiologia , Aromatase/metabolismo , Estrogênios/metabolismo , Peixes/fisiologia , Sistema Imunitário/metabolismo , Estações do Ano , Animais , Feminino , Humanos , Sistemas Neurossecretores/metabolismo , Receptores de Estrogênio/metabolismo , Reprodução/fisiologia
2.
Fish Shellfish Immunol ; 68: 190-201, 2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28698119

RESUMO

Both systemic and locally released steroid hormones, such as cortisol and estrogens, show immunomodulatory actions. This research gives evidence that circulating and leukocyte-derived estrogens can be involved in the regulation of the immune response in common carp, during homeostasis and upon restraining stress. It was found that stress reduced level of blood 17ß-estradiol (E2) and down-regulated the gene expression of components of the "classical" estrogen system: the nuclear estrogen receptors and the aromatase CYP19, in the hypothalamus, the pituitary and in the ovaries. In contrast, higher gene expression of the nuclear estrogen receptors and cyp19a was found in the head kidney of stressed animals. Moreover, stress induced changes in the E2 level and in the estrogen sensitivity at local/leukocyte level. For the first time in fish, we showed the presence of physiologically relevant amounts of E2 and the substrates for its conversion (estrone - E1 and testosterone - T) in head kidney monocytes/macrophages and found that its production is modulated upon stress. Moreover, stress reduced the sensitivity of leukocytes towards estrogens, by down-regulation the expression of the erb and cyp19 genes in carp phagocytes. In contrast, era expression was up-regulated in the head kidney monocytes/macrophages and in PBLs derived from stressed animals. We hypothesize that, the increased expression of ERα, that was observed during stress, can be important for the regulation of leukocyte differentiation, maturation and migration. In conclusion, these results indicate that, in fish, the estrogen network can be actively involved in the regulation of the systemic and local stress response and the immune response.


Assuntos
Aromatase/genética , Carpas/fisiologia , Proteínas de Peixes/genética , Receptores de Estrogênio/genética , Estresse Fisiológico , Animais , Aromatase/metabolismo , Carpas/genética , Carpas/imunologia , Regulação para Baixo , Estrogênios/metabolismo , Proteínas de Peixes/metabolismo , Perfilação da Expressão Gênica , Rim Cefálico/imunologia , Leucócitos/imunologia , Receptores de Estrogênio/metabolismo , Restrição Física
3.
Dev Comp Immunol ; 66: 61-72, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27062969

RESUMO

Estrogens are important for bi-directional neuroendocrine-immune interaction. They act via nuclear estrogen receptors (ERα and ERß) and/or G-protein coupled receptor - GPR30. We found expression of ERα, ERß and GPR30 in carp lymphoid tissues and head kidney monocytes/macrophages, neutrophils and lymphocytes. Interestingly, ERß is also expressed in some head kidney lymphocytes but not in naive PBLs. Immune stimulation altered the cell type specific profile of expression of these receptors, which depends on both activation and maturation stage. This implies direct leukocyte responsiveness to estrogen stimulation and therefore in vitro effects of 17ß-estradiol (E2) on reactive oxygen species (ROS) production in monocytes/macrophages were determined. Short-time incubation with E2 increased ROS production in PMA-stimulated cells. Results comply with mediation by GPR30, partially functioning via phosphoinositide 3-kinase activation. These results furthermore demonstrate that neuroendocrine-immune communication via estrogen receptors is evolutionary conserved.


Assuntos
Carpas/imunologia , Receptor alfa de Estrogênio/metabolismo , Receptor beta de Estrogênio/metabolismo , Proteínas de Peixes/metabolismo , Leucócitos/imunologia , Sistemas Neurossecretores , Receptores Acoplados a Proteínas G/metabolismo , Animais , Evolução Biológica , Células Cultivadas , Estradiol/imunologia , Imunomodulação , Ativação Linfocitária , Neuroimunomodulação/imunologia , Espécies Reativas de Oxigênio/metabolismo
4.
Dev Comp Immunol ; 53(1): 179-90, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-26188098

RESUMO

Melatonin is responsible for the synchronization of many physiological processes, including the immune response. Here we focus on the expression of melatonin MT1 receptors in/on leukocytes, and on the effects of melatonin administration on the inflammatory processes of carp. For the first time, we showed that fish leukocytes express MT1 receptors, implicating direct responsiveness to melatonin stimulation. Moreover, both in vitro and in vivo, melatonin modulated the immune response. The most potent effects of melatonin concerned the regulation of leukocyte migration. Melatonin reduced chemotaxis of leukocytes towards CXC chemokines in vitro. In vivo, during zymosan induced peritonitis, i.p. administration of melatonin reduced the number of neutrophils. This correlated with a melatonin-induced decrease of gene expression of the CXCa chemokine. Moreover, melatonin induced a decrease of the respiratory burst in inflammatory leukocytes. Although these data do suggest a potent anti-inflammatory function for this hormone, melatonin-induced inhibition of leukocyte apoptosis clearly indicates towards a dual function. These results show that also in carp, melatonin performs a pleiotropic and extra-pineal function that is important in maintaining the delicate pro- and anti-inflammatory balance during infection. They furthermore demonstrate that neuroendocrine-immune interaction via melatonin is evolutionary conserved.


Assuntos
Apoptose/efeitos dos fármacos , Carpas/imunologia , Quimiotaxia/efeitos dos fármacos , Leucócitos/imunologia , Melatonina/farmacologia , Receptor MT1 de Melatonina/biossíntese , Animais , Anti-Inflamatórios/farmacologia , Apoptose/imunologia , Quimiocinas CXC/biossíntese , Quimiocinas CXC/imunologia , Quimiotaxia/imunologia , Inflamação/imunologia , Subunidade p35 da Interleucina-12/biossíntese , Ativação de Neutrófilo/efeitos dos fármacos , Neutrófilos/imunologia , Peritonite/induzido quimicamente , Peritonite/imunologia , Explosão Respiratória/efeitos dos fármacos , Explosão Respiratória/imunologia , Fator de Necrose Tumoral alfa/biossíntese , Zimosan
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