RESUMEN
Rationale: The major cause of heart failure is myocardium death consequent to detrimental cardiac remodeling and fibrosis following myocardial infarction. The cardiac protective cytokine interleukin (IL)-33, which signals by ST2 receptor binding, is associated with group 2 innate lymphoid cell (ILC2) activation and regulates tissue homeostasis and repair following tissue injury in various tissues. However, the distribution and role of IL-33-responsive ILC2s in cardiac fibrosis remain unclear. In this study, we elucidated the roles of IL-33-responsive cardiac-resident ILC2s and IL-33-mediated immunomodulatory functions in cardiac fibrosis. Methods: We examined the distribution of cardiac ILC2s by using flow cytometry. The roles of IL-33-mediated ILC2 expansion in cardiac fibrosis was evaluated in the mouse model of catecholamine-induced cardiac fibrosis. ILC-deficient Rag2â/âIL2Rγcâ/â mice were implemented to determine the contribution of endogenous ILC in the progression of cardiac fibrosis. Histopathological assessments, speckle tracking echocardiography, and transcriptome profile analysis were performed to determine the effects of IL-33-mediated cardiac protective functions. Results: We identified the resident cardiac ILC2s, which share similar cell surface marker and transcriptional factor expression characteristics as peripheral blood and lung tissue ILC2s. IL-33 treatment induced ILC2 expansion via ST2. In vivo, ILC-deficient Rag2â/âIL2Rγcâ/â mice developed exacerbated cardiac fibrosis following catecholamine-induced stress cardiac injury. IL-33 treatment expanded cardiac ILC2s and revealed protective effects against cardiac tissue damage with reduced cardiomyocyte death, immune cell infiltration, tissue fibrosis, and improved myocardial function. Transcriptome analysis revealed that IL-33 attenuated extracellular matrix synthesis- and fibroblast activation-associated gene expressions. IL13-knockout or epidermal growth factor receptor (EGFR) inhibition abolished IL-33-mediated cardiac protective function, confirming IL-13 and EGFR signaling as crucial for IL-33-mediated cardioprotective responses. Moreover, ILC2-produced BMP-7 served as a novel anti-fibrotic factor to inhibit TGF-ß1-induced cardiac fibroblast activation. Conclusion: Our findings indicate the presence of IL-33-responsive ILC2s in cardiac tissue and that IL-33-mediated ILC2 expansion affords optimal cardioprotective function via ILC2-derived factors. IL-33-mediated immunomodulation is thus a promising strategy to promote tissue repair and alleviate cardiac fibrosis following acute cardiac injury.
Asunto(s)
Fibrosis/inmunología , Corazón/fisiología , Inmunidad Innata/inmunología , Interleucina-33/inmunología , Linfocitos/inmunología , Miocitos Cardíacos/inmunología , Animales , Catecolaminas/inmunología , Modelos Animales de Enfermedad , Femenino , Pulmón/inmunología , Masculino , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C57BL , Transducción de Señal/inmunología , Transcriptoma/inmunologíaRESUMEN
Based on the lately identified role for the interstitial cells of Cajal (ICCs) of mouse prostate in catecholamine production, as well as the well-established role for the master coregulator metastasis-associated protein 1 (MTA1) in inflammation, we probed into the functional link between aberrant MTA1 expression and pathogenesis of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) using both a MTA1-/- mouse model of experimental autoimmune prostatitis (EAP) and an in vitro chronic prostatitis model in cultured murine ICCs. EAP-induced MTA1 expression was enriched in ICCs of mouse prostate. EAP resulted in a higher increase in the pelvic pain response in MTA1-/- mice compared to WT mice. Consistently, the ICCs from MTA1-/- mice produced higher levels of catecholamines upon induction of in vitro chronic prostatitis. Mechanistically, MTA1 could directly suppress the transcription of Aadc, a rate-limiting enzyme during catecholamine synthesis, in a HDAC2-depdendent manner. Importantly, treatment with AADC inhibitor NSD-1015 significantly ameliorated EAP-elicited pain response and catecholamine overactivity in MTA1-/- mice. Taken together, our findings reveal an inherent regulatory role of the MTA1/AADC pathway in the maintenance of catecholamine production homeostasis in prostate ICCs, and also point to a potential use of HDAC inhibitors and/or AADC inhibitors to treat CP/CPPS.
Asunto(s)
Descarboxilasas de Aminoácido-L-Aromático/genética , Catecolaminas/inmunología , Células Intersticiales de Cajal/inmunología , Prostatitis/inmunología , Proteínas Represoras/inmunología , Transactivadores/inmunología , Animales , Descarboxilasas de Aminoácido-L-Aromático/inmunología , Enfermedades Autoinmunes/genética , Enfermedades Autoinmunes/inmunología , Enfermedades Autoinmunes/patología , Enfermedad Crónica , Regulación hacia Abajo , Eliminación de Gen , Células Intersticiales de Cajal/patología , Masculino , Ratones , Ratones Endogámicos C57BL , Próstata/inmunología , Próstata/patología , Prostatitis/genética , Prostatitis/patología , Proteínas Represoras/genética , Transactivadores/genética , Activación TranscripcionalRESUMEN
Evidence supporting the use of ß2AR agonists in synucleinopathies is rapidly growing. Findings come from different scientific approaches. Molecular and immunological data suggest that adrenergic stimulation may decrease both α-synuclein (α-syn) deposition and pro-inflammatory/neurotoxic molecules release. Small open label clinical trials including a total number of 25 Parkinson's disease (PD) patients, in which the ß2AR agonist salbutamol was added to levodopa, suggest a promising symptomatic benefit. In line with these findings, epidemiological studies investigating the risk of PD development suggest that long term exposure to the agonist salbutamol might be protective, while the antagonist propranolol possibly detrimental. Nonetheless, in both lines of investigation the studies performed so far present important limitations. On the clinical side, large randomized controlled trials are lacking, whereas on the epidemiological side the presence of co-morbid conditions (i.e. smoking and essential tremor) potentially influencing PD risk should taken into consideration. In summary, it is our opinion that ß2AR stimulation in synucleinopathies has a rationale and therefore merits further investigation. Graphical Abstract.
Asunto(s)
Agonistas de Receptores Adrenérgicos beta 2/uso terapéutico , Enfermedad de Parkinson/tratamiento farmacológico , Enfermedad de Parkinson/inmunología , Sinucleinopatías/tratamiento farmacológico , Sinucleinopatías/inmunología , Agonistas de Receptores Adrenérgicos beta 2/farmacología , Animales , Catecolaminas/inmunología , Ensayos Clínicos como Asunto/métodos , Humanos , Receptores Adrenérgicos beta 2/inmunología , Linfocitos T/efectos de los fármacos , Linfocitos T/inmunologíaRESUMEN
Reaction of mast cells of adult male Wistar rats (n=15) in the zone of polypropylene mesh fixation was studied by histochemical, immunohistochemical, and traditional morphological methods on days 1, 5, 10, and 30 after implantation. Immediately after the intervention, mast cells stimulated the processes aimed at wound healing. Secretion of mast cells was clearly regulatory. These cells migrated to the zone of injury for subsequent activation of their function. The number of cNOS+ mast cells near the polypropylene mesh was maximum on day 1 and the number of iNOS+ mast cells peaked on day 5 of the experiment, which probably represented a compensatory reaction. Presumably, stimulation of fibrillogenesis was largely due to the activatory effect of mast cells on the fibroblast function, but not to collagen production by these mast cells.
Asunto(s)
Materiales Biocompatibles/farmacología , Expresión Génica/efectos de los fármacos , Mastocitos/efectos de los fármacos , Polipropilenos/farmacología , Mallas Quirúrgicas , Pared Abdominal/cirugía , Animales , Catecolaminas/inmunología , Catecolaminas/metabolismo , Movimiento Celular/efectos de los fármacos , Colágeno/genética , Colágeno/inmunología , Inflamación , Masculino , Mastocitos/inmunología , NADPH Deshidrogenasa/genética , NADPH Deshidrogenasa/inmunología , Óxido Nítrico Sintasa de Tipo II/genética , Óxido Nítrico Sintasa de Tipo II/inmunología , Óxido Nítrico Sintasa de Tipo III/genética , Óxido Nítrico Sintasa de Tipo III/inmunología , Ratas , Ratas Wistar , Cicatrización de Heridas/efectos de los fármacos , Cicatrización de Heridas/inmunologíaRESUMEN
Acute exercise preferentially mobilizes cytotoxic T-cells, NK-cells and non-classical monocytes to the bloodstream under the influence of hemodynamic forces and/or ß2-adrenergic receptor (ß2-AR) signaling. However, the relative contribution of these mechanisms to the redeployment of the most exercise-responsive cell types is largely unknown. We determined the lymphocyte and monocyte subtypes mobilized to blood during exercise via ß2-AR signaling whilst controlling for ß1-AR mediated reductions in hemodynamic forces. In a randomized, double blind, complete cross-over design, 14 healthy cyclists exercised for 30-minutes at +10% of blood lactate threshold after ingesting: (1) a placebo, (2) a ß1-preferential antagonist (10â¯mg bisoprolol), or (2) a non-preferential ß1â¯+â¯ß2-antagonist (80â¯mg nadolol) across three trials separated by >7-days. Bisoprolol was administered to reduce hemodynamic forces (heart rate and blood pressure) during exercise to levels comparable with nadolol but without blocking ß2-ARs. The mobilization of total NK-cells, terminally differentiated (CD57+) NK-cells, central memory, effector memory and CD45RA+ effector memory CD8+ T-cells; non-classical monocytes; and γδ T-cells were significantly blunted or abrogated under nadolol compared to both bisoprolol and placebo, indicating that the exercise-induced mobilization of these cell types to the blood is largely influenced by ß2-AR signaling. Nadolol failed to inhibit the mobilization of classical monocytes, CD4+ T-cells (and their subsets) or naïve CD8+ T-cells, indicating that these cell types are mobilized with exercise independently of the ß2-AR. We conclude that the preferential mobilization of NK-cells, non-classical monocytes and differentiated subsets of CD8+ T-cells with exercise is largely dependent on catecholamine signaling through the ß2-AR. These findings provide mechanistic insights by which distinct lymphocyte and monocyte subtypes are preferentially mobilized to protect the host from anticipated injury or infection in response to an acute stress response.
Asunto(s)
Linfocitos T CD8-positivos/inmunología , Ejercicio Físico/fisiología , Células Asesinas Naturales/inmunología , Monocitos/inmunología , Receptores Adrenérgicos beta 2/inmunología , Adulto , Bisoprolol/farmacología , Linfocitos T CD8-positivos/metabolismo , Catecolaminas/inmunología , Catecolaminas/metabolismo , Estudios Cruzados , Método Doble Ciego , Femenino , Voluntarios Sanos , Humanos , Células Asesinas Naturales/metabolismo , Activación de Linfocitos , Masculino , Monocitos/metabolismo , Nadolol/farmacología , Receptores Adrenérgicos beta 2/metabolismo , Transducción de SeñalRESUMEN
OBJECTIVE: The aim of this study is to analyze the immune-endocrine profile in neurocysticercosis (NC) patients resistant to cysticidal treatment. METHODS: The inflammatory and regulatory responses of 8 resistant NC patients with extraparenchymal parasites and 5 healthy controls were evaluated through flow cytometry. Serum interleukin levels were measured by ELISA and catecholamines levels by high performance liquid chromatography. RESULTS: Higher percentages of Tr1, CD4+CD25+FOXP3+CD127- and CD4+CD45RO+FOXP3HI were found in NC patients compared with healthy controls, but no difference was found in catecholamine levels. Antigen-specific proliferative immune response was observed in NC patients. Neither anti-inflammatory nor pro-inflammatory cytokines showed differences between patients and controls, but IL-6 levels were lower in treatment-resistant NC patients. In addition, TGFß showed a significant negative correlation with dopamine. CONCLUSIONS: Altogether, these results may point to a modulation of the neuroinflammation in these patients that could indirectly favor cysticercal survival in CNS microenvironment.
Asunto(s)
Antiparasitarios/uso terapéutico , Inmunidad Celular/inmunología , Mediadores de Inflamación/sangre , Mediadores de Inflamación/inmunología , Neurocisticercosis/sangre , Neurocisticercosis/inmunología , Adulto , Anciano , Antiparasitarios/farmacología , Biomarcadores/sangre , Catecolaminas/sangre , Catecolaminas/inmunología , Femenino , Humanos , Inmunidad Celular/efectos de los fármacos , Masculino , Persona de Mediana Edad , Neurocisticercosis/tratamiento farmacológico , Linfocitos T/efectos de los fármacos , Linfocitos T/inmunología , Linfocitos T/metabolismo , Resultado del TratamientoRESUMEN
In a previous work using guinea pig prostate, we have identified a novel interstitial cells of Cajal (ICCs) which possess close contacts between sympathetic nerve bundles and smooth muscle cells. The ability of prostatic ICCs in mediating excitatory neural inputs was therefore studied using isolated murine prostate ICCs by collagenase digestion combined with FACS method. RT-PCR and Western blotting analyses revealed that prostatic ICCs under a quiescent state expressed abundantly the rate-limiting enzymes essential for catecholamine synthesis. Moreover, distinct proinflammatory cytokines (e.g. IL-1ß, IL-8, ICAM-1 and TNF-α) could significantly stimulate the expression levels of the rate-limiting enzymes of catecholamine production in prostate ICCs. Mechanistically, the above-mentioned stimulatory effects of proinflammatory cytokines appeared to be mediated via activation of NF-κB, HIF-1α and HDACs signaling pathways. Considering that prostatic catecholamine overactivity serves as an essential etiology of pelvic pain by indirectly stimulating the smooth muscle cell proliferation, or by directly causing muscular spasm, our results collectively suggest that targeting the NF-κB, HIF-1α and HDACs pathways in prostate ICCs be considered as a new strategy for treatment of chronic pelvic pain syndrome (CPPS) induced by chronic prostatitis (CP). Overall, the current study should shed novel light on the biology of this unique prostate ICCs.
Asunto(s)
Catecolaminas/inmunología , Dolor Crónico/fisiopatología , Citocinas/inmunología , Células Intersticiales de Cajal/patología , Dolor Pélvico/fisiopatología , Prostatitis/fisiopatología , Animales , Catecolaminas/análisis , Células Cultivadas , Enfermedad Crónica , Dolor Crónico/etiología , Dolor Crónico/inmunología , Citocinas/análisis , Células Intersticiales de Cajal/inmunología , Masculino , Ratones Endogámicos C57BL , Dolor Pélvico/etiología , Dolor Pélvico/inmunología , Próstata/citología , Próstata/inmunología , Próstata/fisiopatología , Prostatitis/complicaciones , Prostatitis/inmunologíaAsunto(s)
Macrófagos/inmunología , Monocitos/inmunología , Tejido Adiposo Blanco/citología , Tejido Adiposo Blanco/inmunología , Tejido Adiposo Blanco/inervación , Animales , Catecolaminas/inmunología , Diferenciación Celular/inmunología , Supervivencia Celular/inmunología , Humanos , Macrófagos/clasificación , Macrófagos/metabolismo , Ratones , Modelos Inmunológicos , Monocitos/clasificación , Monocitos/metabolismo , NeuroinmunomodulaciónRESUMEN
The physiological changes that occur immediately following cancer surgeries initiate a chain of events that ultimately result in a short pro-, followed by a prolonged anti-, inflammatory period. Natural Killer (NK) cells are severely affected during this period in the recovering cancer patient. NK cells play a crucial role in anti-tumour immunity because of their innate ability to differentiate between malignant versus normal cells. Therefore, an opportunity arises in the aftermath of cancer surgery for residual cancer cells, including distant metastases, to gain a foothold in the absence of NK cell surveillance. Here, we describe the post-operative environment and how the release of sympathetic stress-related factors (e.g., cortisol, prostaglandins, catecholamines), anti-inflammatory cytokines (e.g., IL-6, TGF-ß), and myeloid derived suppressor cells, mediate NK cell dysfunction. A snapshot of current and recently completed clinical trials specifically addressing NK cell dysfunction post-surgery is also discussed. In collecting and summarizing results from these different aspects of the surgical stress response, a comprehensive view of the NK cell suppressive effects of surgery is presented. Peri-operative therapies to mitigate NK cell suppression in the post-operative period could improve curative outcomes following cancer surgery.
Asunto(s)
Diferenciación Celular/inmunología , Células Asesinas Naturales/inmunología , Neoplasias/inmunología , Catecolaminas/inmunología , Catecolaminas/metabolismo , Humanos , Hidrocortisona/inmunología , Hidrocortisona/metabolismo , Células Asesinas Naturales/patología , Células Mieloides/inmunología , Células Mieloides/patología , Neoplasias/patología , Neoplasias/cirugía , Periodo Posoperatorio , Prostaglandinas/inmunología , Prostaglandinas/metabolismoRESUMEN
OBJECTIVE: To investigate the effect of military stress on immune response and Helicobacter pylori stomach infections. METHODS: In this prospective, observational study, the Symptom Checklist-90 questionnaire was completed by military recruits before and following a 3-month basic training programme. H. pylori immunoglobulin (Ig)G levels, C(14)-urea breath-test values and levels of cortisol, catecholamine, and certain humoral and cellular immune responses were measured before and after the basic training. RESULTS: For 60 military recruits, somatization, depression and paranoid ideation scores were significantly increased after, compared with before, basic training. Post-training H. pylori IgG detection revealed three additional cases of H. pylori infection. Post-training C(14)-urea breath-test values were significantly higher compared with before training - thus suggesting higher levels of H. pylori colonization in the stomach. Post-training cortisol and catecholamine levels were increased, while serum IgG levels were decreased; complement component (C)3 and C4 levels remained unchanged. Post-training CD4(+) and CD8(+) T-cell percentages and the CD4(+)/CD8(+) ratio were significantly reduced compared with before training. Serum interleukin (IL)-2 levels were lower and IL-10 levels were higher following training and there was a significant decrease in the IL-2/IL-10 ratio. CONCLUSION: Military stress may reduce humoral and cellular immune responses and may aggravate the severity of H. pylori infection.
Asunto(s)
Anticuerpos Antibacterianos/sangre , Depresión/inmunología , Infecciones por Helicobacter/inmunología , Inmunoglobulina G/sangre , Personal Militar/psicología , Estómago/inmunología , Estrés Psicológico/inmunología , Adolescente , Pruebas Respiratorias , Relación CD4-CD8 , Catecolaminas/sangre , Catecolaminas/inmunología , Complemento C3/inmunología , Complemento C3/metabolismo , Complemento C4/inmunología , Complemento C4/metabolismo , Depresión/complicaciones , Depresión/patología , Depresión/psicología , Infecciones por Helicobacter/complicaciones , Infecciones por Helicobacter/microbiología , Infecciones por Helicobacter/patología , Helicobacter pylori/inmunología , Humanos , Hidrocortisona/sangre , Hidrocortisona/inmunología , Inmunidad Humoral , Inmunidad Innata , Interleucina-10/sangre , Interleucina-10/inmunología , Interleucina-2/sangre , Interleucina-2/inmunología , Masculino , Estudios Prospectivos , Entrenamiento de Fuerza , Estómago/microbiología , Estómago/patología , Estrés Psicológico/complicaciones , Estrés Psicológico/patología , Estrés Psicológico/psicología , Urea/metabolismo , Adulto JovenRESUMEN
Bordetella bronchiseptica can use catecholamines to obtain iron from transferrin and lactoferrin via uptake pathways involving the BfrA, BfrD, and BfrE outer membrane receptor proteins, and although Bordetella pertussis has the bfrD and bfrE genes, the role of these genes in iron uptake has not been demonstrated. In this study, the bfrD and bfrE genes of B. pertussis were shown to be functional in B. bronchiseptica, but neither B. bronchiseptica bfrD nor bfrE imparted catecholamine utilization to B. pertussis. Gene fusion analyses found that expression of B. bronchiseptica bfrA was increased during iron starvation, as is common for iron receptor genes, but that expression of the bfrD and bfrE genes of both species was decreased during iron limitation. As shown previously for B. pertussis, bfrD expression in B. bronchiseptica was also dependent on the BvgAS virulence regulatory system; however, in contrast to the case in B. pertussis, the known modulators nicotinic acid and sulfate, which silence Bvg-activated genes, did not silence expression of bfrD in B. bronchiseptica. Further studies using a B. bronchiseptica bvgAS mutant expressing the B. pertussis bvgAS genes revealed that the interspecies differences in bfrD modulation are partly due to BvgAS differences. Mouse respiratory infection experiments determined that catecholamine utilization contributes to the in vivo fitness of B. bronchiseptica and B. pertussis. Additional evidence of the in vivo importance of the B. pertussis receptors was obtained from serologic studies demonstrating pertussis patient serum reactivity with the B. pertussis BfrD and BfrE proteins.
Asunto(s)
Proteínas de la Membrana Bacteriana Externa/inmunología , Infecciones por Bordetella/inmunología , Bordetella bronchiseptica/patogenicidad , Bordetella pertussis/patogenicidad , Regulación Bacteriana de la Expresión Génica , Receptores de Catecolaminas/inmunología , Receptores de Superficie Celular/inmunología , Animales , Proteínas de la Membrana Bacteriana Externa/genética , Proteínas Bacterianas/genética , Proteínas Bacterianas/inmunología , Infecciones por Bordetella/microbiología , Infecciones por Bordetella/patología , Bordetella bronchiseptica/genética , Bordetella bronchiseptica/inmunología , Bordetella bronchiseptica/metabolismo , Bordetella pertussis/genética , Bordetella pertussis/inmunología , Bordetella pertussis/metabolismo , Catecolaminas/inmunología , Catecolaminas/metabolismo , Humanos , Hierro/inmunología , Hierro/metabolismo , Ratones , Ratones Endogámicos BALB C , Isoformas de Proteínas/genética , Isoformas de Proteínas/inmunología , Receptores de Catecolaminas/genética , Receptores de Superficie Celular/genética , Sideróforos/inmunología , Sideróforos/metabolismo , Especificidad de la Especie , Factores de Transcripción/genética , Factores de Transcripción/inmunología , VirulenciaRESUMEN
The neurophysiological response of an animal to stress involves the production of a number of stress-related neurochemicals including the catecholamines norepinephrine and epinephrine. It is generally believed that such neurochemicals belong exclusively to the animal kingdom and that any role such neurochemicals play in the infective process is largely confined to host physiology and immunology-related parameters. This, however, is wholly incorrect as many of the bacterial species that are known to cause infections possess the capacity to not only recognize neuroendocrine hormones produced by the host in response to stress, but also synthesize the very same neurochemicals. Given this, infectious microorganisms are capable of directly responding to the neurochemical outflow resulting from a stress event and initiating pathogenic processes. Although the neuroendocrine environment of the lung following a stress event is not fully understood, it most likely possesses abundant levels of stress-related neurochemicals due to its rich blood supply and rich noradrenergic tissue innervation. The ability of microorganisms to recognize and produce neurochemicals that can influence the host, known as microbial endocrinology, provides for a mechanistic basis with which to examine the ability of stress to influence health and susceptibility to disease.
Asunto(s)
Catecolaminas/fisiología , Interacciones Huésped-Patógeno/fisiología , Estrés Fisiológico/fisiología , Animales , Catecolaminas/inmunología , Bovinos , Enfermedades de los Bovinos/inmunología , Enfermedades de los Bovinos/microbiología , Interacciones Huésped-Patógeno/inmunología , Pulmón/inmunología , Pulmón/inervación , Pulmón/microbiología , Microbiota/fisiología , Estrés Fisiológico/inmunologíaRESUMEN
The sympathetic nervous system (SNS) is part of an integrative network that functions to restore homeostasis following injury and infection. The SNS can provide negative feedback control over inflammation through the secretion of catecholamines from postganglionic sympathetic neurons and adrenal chromaffin cells (ACCs). Central autonomic structures receive information regarding the inflammatory status of the body and reflexively modulate SNS activity. However, inflammation and infection can also directly regulate SNS function by peripheral actions on postganglionic cells. The present review discusses how inflammation activates autonomic reflex pathways and compares the effect of localized and systemic inflammation on ACCs and postganglionic sympathetic neurons. Systemic inflammation significantly enhanced catecholamine secretion through an increase in Ca(2+) release from the endoplasmic reticulum. In contrast, acute and chronic GI inflammation reduced voltage-gated Ca(2+) current. Thus it appears that the mechanisms underlying the effects of peripheral and systemic inflammation neuroendocrine function converge on the modulation of intracellular Ca(2+) signaling.
Asunto(s)
Calcio/metabolismo , Catecolaminas/metabolismo , Enfermedades Inflamatorias del Intestino/metabolismo , Neuronas/metabolismo , Sepsis/metabolismo , Sistema Nervioso Simpático/metabolismo , Animales , Calcio/inmunología , Señalización del Calcio , Catecolaminas/inmunología , Células Cromafines/inmunología , Células Cromafines/metabolismo , Células Cromafines/patología , Citocinas/genética , Citocinas/inmunología , Retroalimentación Fisiológica , Regulación de la Expresión Génica , Humanos , Inflamación/genética , Inflamación/inmunología , Inflamación/metabolismo , Inflamación/patología , Enfermedades Inflamatorias del Intestino/genética , Enfermedades Inflamatorias del Intestino/inmunología , Enfermedades Inflamatorias del Intestino/patología , Neuronas/inmunología , Neuronas/patología , Sepsis/genética , Sepsis/inmunología , Sepsis/patología , Sistema Nervioso Simpático/inmunología , Sistema Nervioso Simpático/patologíaRESUMEN
Cells constitutively release small (40-100 nm) vesicles known as exosomes, but their composition and function changes in response to a variety of physiological challenges, such as injury, infection, and disease. Advances in our understanding of the immunological relevance of exosomes have been made, however, few studies have explored their role in stress physiology. Exposure to a variety of acute stressors facilitates the efficacy of innate immune responses, but the mechanisms for these effects are not fully understood. Since exosomes are emerging as important inflammatory mediators, they likely exhibit a similar role when an organism is exposed to an acute stressor. Here, we review our current knowledge of the basic properties and immunological functions of exosomes and provide emerging data supporting the role of stress-modified exosomes in regulating the innate immune response, potentially enabling long-distance cellular communication and obviating the need for direct cell-to-cell contact.
Asunto(s)
Exosomas/inmunología , Proteínas del Choque Térmico HSP72/inmunología , Inmunidad Innata/genética , MicroARNs/inmunología , Estrés Fisiológico/inmunología , Sistema Nervioso Simpático/inmunología , Animales , Catecolaminas/inmunología , Catecolaminas/metabolismo , Comunicación Celular , Exosomas/metabolismo , Regulación de la Expresión Génica , Proteínas del Choque Térmico HSP72/genética , Humanos , Inmunomodulación , MicroARNs/genética , Transducción de Señal , Estrés Fisiológico/genética , Sistema Nervioso Simpático/metabolismoRESUMEN
The economical and phylogenic importance of mollusc has led an increasing number of investigations giving emphasis to immune defense mechanism. This review discusses the advances in immunological study of mollusc in China, with special reference to dominant aquaculture species over the past decades. As an invertebrate group, molluscs lack adaptive immunity and consequently they have evolved sophisticated strategies of innate immunity for defense against pathogens. This review aims to present the various immunologically significant pattern recognition receptors (PRRs), such as Toll-like receptors (TLRs), lectins, lipopolysaccharide and ß-1, 3-glucan binding protein (LGBP), scavenger receptors (SRs) employed by mollucans. This work also highlights immune proteolytic cascade, TLR signaling pathway and an extensive repertoire of immune effectors including antimicrobial peptide, lysozyme, antioxidant enzyme and heat shock protein. Further, the review presents the preliminary progress made on the catecholaminergic neuroendocrine system in scallop and its immunomodulation function to throw light into neuroendocrine-immune regulatory network in lower invertebrates.
Asunto(s)
Catecolaminas/inmunología , Moluscos/inmunología , Sistemas Neurosecretores/inmunología , Receptores de Reconocimiento de Patrones/inmunología , Animales , Investigación Biomédica/tendencias , China , Interacciones Huésped-Patógeno , Humanos , Inmunidad Innata , Inmunomodulación , Neuroinmunomodulación , Transducción de Señal/inmunologíaRESUMEN
BACKGROUND: Vitiligo is a highly complex multifactorial condition of the skin that has an unclear mechanism of pathogenesis. OBJECTIVE: This review summarizes the role of various neurogenic inflammatory factors significantly upregulated in vitiligo. METHODS: A literature review was conducted of all pertinent data regarding neuropeptides that are altered in vitiligo and their possible role in the destruction of melanocytes. RESULTS: The close associations between the skin, immune system, and nervous system, along with specific changes demonstrated in vitiligo patients, support a pathogenic mechanism of vitiligo that involves neuroimmunologic factors, the release of which can be governed by mental stress. CONCLUSION: Neuropeptides and nerve growth factors are critical regulators of emotional response and may precipitate the onset and development of vitiligo in certain predisposed individuals. More studies are required to investigate whether a direct link exists between genetics, mental stress, and neurogenic factors in vitiligo.
Asunto(s)
Inflamación Neurogénica/inmunología , Vitíligo/inmunología , Péptido Relacionado con Gen de Calcitonina/inmunología , Catecolaminas/inmunología , Susceptibilidad a Enfermedades , Humanos , Melanocitos/inmunología , Factor de Crecimiento Nervioso/inmunología , Neuropéptido Y/inmunología , Vitíligo/metabolismo , Vitíligo/psicología , Vitíligo/terapiaRESUMEN
Catecholamines are pivotal signal molecules in the neuroendocrine-immune regulatory network, and implicated in the modulation of immune response. In the present study, the activities of some immune-related enzymes and the concentration of catecholamines were determined in circulating haemolymph of scallops Chlamys farreri after bacteria Vibrio anguillarum challenge. The activities of superoxide dismutase (SOD), catalase (CAT) and lysozyme (LYZ) increased significantly and reached 610 U mg(-1) at 12 h, 37.6 U mg(-1) at 6 h and 261.5 U mg(-1) at 6 h after bacteria challenge, respectively. The concentration of norepinephrine, epinephrine and dopamine also increased significantly and reached 114.9 ng mL(-1) at 12 h, 86.9 ng mL(-1) at 24 h and 480.4 pg mL(-1) at 12 h after bacteria challenge, respectively. Meanwhile, the activities of these immune-related enzymes in haemolymph were monitored in those scallops which were challenged by bacteria V. anguillarum and stimulated simultaneously with norepinephrine, epinephrine and adrenoceptor antagonist. The injection of norepinephrine and epinephrine repressed significantly the induction of bacteria challenge on the activities of immune-related enzymes, and they were reduced to about half of that in the control groups. The blocking of α and ß-adrenoceptor by antagonist only repressed the increase of CAT and LYZ activities significantly, while no significant effect was observed on the increase of SOD activities. The collective results indicated that scallop catecholaminergic neuroendocrine system could be activated by bacteria challenge to release catecholamines after the immune response had been triggered, and the immune response against bacteria challenge could been negatively modulated by norepinephrine, epinephrine, and adrenoceptor antagonist. This information is helpful to further understand the immunomodulation of catecholamines in scallops.
Asunto(s)
Catecolaminas/inmunología , Inmunomodulación/inmunología , Pectinidae/inmunología , Pectinidae/microbiología , Vibrio/inmunología , Antagonistas Adrenérgicos/farmacología , Análisis de Varianza , Animales , Catalasa/sangre , Catecolaminas/sangre , Dopamina/farmacología , Ensayo de Inmunoadsorción Enzimática , Epinefrina/farmacología , Inmunomodulación/efectos de los fármacos , Muramidasa/sangre , Norepinefrina/farmacología , Superóxido Dismutasa/sangreRESUMEN
This article reviews the interaction between the neuroendocrine and immune systems in response to exercise stress, considering gender differences. The body's response to exercise stress is a system-wide effort coordinated by the integration between the immune and the neuroendocrine systems. Although considered distinct systems, increasing evidence supports the close communication between them. Like any stressor, the body's response to exercise triggers a systematic series of neuroendocrine and immune events directed at bringing the system back to a state of homeostasis. Physical exercise presents a unique physiological stress where the neuroendocrine and immune systems contribute to accommodating the increase in physiological demands. These systems of the body also adapt to chronic overload, or exercise training. Such adaptations alleviate the magnitude of subsequent stress or minimize the exercise challenge to within homeostatic limits. This adaptive capacity of collaborating systems resembles the acquired, or adaptive, branch of the immune system, characterized by the memory capacity of the cells involved. Specific to the adaptive immune response, once a specific antigen is encountered, memory cells, or lymphocytes, mount a response that reduces the magnitude of the immune response to subsequent encounters of the same stress. In each case, the endocrine response to physical exercise and the adaptive branch of the immune system share the ability to adapt to a stressful encounter. Moreover, each of these systemic responses to stress is influenced by gender. In both the neuroendocrine responses to exercise and the adaptive (B lymphocyte) immune response, gender differences have been attributed to the 'protective' effects of estrogens. Thus, this review will create a paradigm to explain the neuroendocrine communication with leukocytes during exercise by reviewing (i) endocrine and immune interactions; (ii) endocrine and immune systems response to physiological stress; and (iii) gender differences (and the role of estrogen) in both endocrine response to physiological stress and adaptive immune response.