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1.
EMBO J ; 34(7): 881-95, 2015 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-25666591

RESUMEN

Intestinal immune regulatory signals govern gut homeostasis. Breakdown of such regulatory mechanisms may result in inflammatory bowel disease (IBD). Lactobacillus acidophilus contains unique surface layer proteins (Slps), including SlpA, SlpB, SlpX, and lipoteichoic acid (LTA), which interact with pattern recognition receptors to mobilize immune responses. Here, to elucidate the role of SlpA in protective immune regulation, the NCK2187 strain, which solely expresses SlpA, was generated. NCK2187 and its purified SlpA bind to the C-type lectin SIGNR3 to exert regulatory signals that result in mitigation of colitis, maintenance of healthy gastrointestinal microbiota, and protected gut mucosal barrier function. However, such protection was not observed in Signr3(-/-) mice, suggesting that the SlpA/SIGNR3 interaction plays a key regulatory role in colitis. Our work presents critical insights into SlpA/SIGNR3-induced responses that are integral to the potential development of novel biological therapies for autoinflammatory diseases, including IBD.


Asunto(s)
Antígenos CD/inmunología , Proteínas Bacterianas/inmunología , Enfermedades Inflamatorias del Intestino/inmunología , Mucosa Intestinal/inmunología , Lactobacillus acidophilus/inmunología , Lectinas Tipo C/inmunología , Animales , Antígenos CD/genética , Proteínas Bacterianas/genética , Enfermedades Inflamatorias del Intestino/genética , Enfermedades Inflamatorias del Intestino/microbiología , Enfermedades Inflamatorias del Intestino/patología , Mucosa Intestinal/patología , Lactobacillus acidophilus/genética , Lectinas Tipo C/genética , Lipopolisacáridos/genética , Lipopolisacáridos/inmunología , Ratones , Ratones Noqueados , Unión Proteica/genética , Unión Proteica/inmunología , Ácidos Teicoicos/genética , Ácidos Teicoicos/inmunología
2.
Semin Cell Dev Biol ; 49: 44-51, 2016 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-26709005

RESUMEN

The gastrointestinal (GI) tract must balance the extraction of energy and metabolic end-products from ingested nutrition and resident gut microbes and the maintenance of a symbiotic relationship with this microbiota, with the ability to mount functional immune responses to pathogenic organisms to maintain GI health. The gut epithelium is equipped with bacteria-sensing mechanisms that discriminate between pathogenic and commensal microorganisms and regulate host responses between immunity and tolerance. The epithelium also expresses numerous nutrient-sensing receptors, but their importance in the preservation of the gut microbiota and immune homeostasis remains largely unexplored. Observations that a deficiency in the extracellular calcium-sensing receptor (CaSR) using intestinal epithelium-specific receptor knockout mice resulted in diminished intestinal barrier integrity, altered composition of the gut microbiota, modified expression of intestinal pattern recognition receptors, and a skewing of local and systemic innate responses from regulatory to stimulatory, may change the way that this receptor is considered as a potential immunotherapeutic target in gut homeostasis. These findings suggest that pharmacologic CaSR activators and CaSR-based nutrients such as calcium, polyamines, phenylalanine, tryptophan, and oligo-peptides might be useful in conditioning the gut microenvironment, and thus, in the prevention and treatment of disorders such as inflammatory bowel disease (IBD), infectious enterocolitis, and other inflammatory and secretory diarrheal diseases. Here, we review the emerging roles of the CaSR in intestinal homeostasis and its therapeutic potential for gut pathology.


Asunto(s)
Colitis/inmunología , Tracto Gastrointestinal/inmunología , Receptores Sensibles al Calcio/fisiología , Animales , Colitis/metabolismo , Neoplasias Colorrectales/inmunología , Neoplasias Colorrectales/metabolismo , Diarrea/inmunología , Diarrea/metabolismo , Tracto Gastrointestinal/metabolismo , Humanos , Enfermedades Inflamatorias del Intestino , Mucosa Intestinal/inmunología , Mucosa Intestinal/metabolismo , Transducción de Señal
3.
Physiol Genomics ; 48(7): 526-36, 2016 07 01.
Artículo en Inglés | MEDLINE | ID: mdl-27235450

RESUMEN

Hypertension (HTN) is a prevalent condition with complex etiology and pathophysiology. Evidence exists of significant communication between the nervous system and the immune system (IS), and there appears to be a direct role for inflammatory bone marrow (BM) cells in the pathophysiology of hypertension. However, the molecular and neural mechanisms underlying this interaction have not been characterized. Here, we transplanted whole BM cells from the beta 1 and 2 adrenergic receptor (AdrB1(tm1Bkk)AdrB2(tm1Bkk)/J) knockout (KO) mice into near lethally irradiated C57BL/6J mice to generate a BM AdrB1.B2 KO chimera. This allowed us to evaluate the role of the BM beta 1 and beta 2 adrenergic receptors in mediating BM IS homeostasis and regulating blood pressure (BP) in an otherwise intact physiological setting. Fluorescence-activated cell sorting demonstrated that a decrease in systolic and mean BP in the AdrB1.B2 KO chimera is associated with a decrease in circulating inflammatory T cells, macrophage/monocytes, and neutrophils. Transcriptomics in the BM identified 7,419 differentially expressed transcripts between the C57 and AdrB1.B2 KO chimera. Pathway analysis revealed differentially expressed transcripts related to several cell processes in the BM of C57 compared with AdrB1.B2 KO chimera, including processes related to immunity (e.g., T-cell activation, T-cell recruitment, cytokine production, leukocyte migration and function), the cardiovascular system (e.g., blood vessel development, peripheral nerve blood flow), and the brain (e.g., central nervous system development, neurite development) among others. This study generates new insight into the molecular events that underlie the interaction between the sympathetic drive and IS in modulation of BP.


Asunto(s)
Presión Sanguínea/genética , Médula Ósea/metabolismo , Redes Reguladoras de Genes/genética , Inflamación/genética , Receptores Adrenérgicos beta 1/genética , Receptores Adrenérgicos beta 2/genética , Transcripción Genética/genética , Animales , Células de la Médula Ósea/metabolismo , Trasplante de Médula Ósea/métodos , Modelos Animales de Enfermedad , Hipertensión/genética , Hipertensión/metabolismo , Inflamación/metabolismo , Macrófagos/metabolismo , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Monocitos/metabolismo , Neutrófilos/metabolismo
4.
Proc Natl Acad Sci U S A ; 109(26): 10462-7, 2012 Jun 26.
Artículo en Inglés | MEDLINE | ID: mdl-22689992

RESUMEN

An imbalance of commensal bacteria and their gene products underlies mucosal and, in particular, gastrointestinal inflammation and a predisposition to cancer. Lactobacillus species have received considerable attention as examples of beneficial microbiota. We have reported previously that deletion of the phosphoglycerol transferase gene that is responsible for lipoteichoic acid (LTA) biosynthesis in Lactobacillus acidophilus (NCK2025) rendered this bacterium able to significantly protect mice against induced colitis when delivered orally. Here we report that oral treatment with LTA-deficient NCK2025 normalizes innate and adaptive pathogenic immune responses and causes regression of established colonic polyps. This study reveals the proinflammatory role of LTA and the ability of LTA-deficient L. acidophilus to regulate inflammation and protect against colonic polyposis in a unique mouse model.


Asunto(s)
Poliposis Adenomatosa del Colon/inmunología , Lactobacillus acidophilus/genética , Lipopolisacáridos/genética , Ácidos Teicoicos/genética , Poliposis Adenomatosa del Colon/patología , Animales , Ratones , Linfocitos T Reguladores/inmunología
5.
J Infect Dis ; 210(9): 1499-507, 2014 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-24829464

RESUMEN

Ingestion of Bacillus anthracis spores causes gastrointestinal (GI) anthrax. Humoral immune responses, particularly immunoglobulin A (IgA)-secreting B-1 cells, play a critical role in the clearance of GI pathogens. Here, we investigated whether B. anthracis impacts the function of colonic B-1 cells to establish active infection. GI anthrax led to significant inhibition of immunoglobulins (eg, IgA) and increased expression of program death 1 on B-1 cells. Furthermore, infection also diminished type 2 innate lymphoid cells (ILC2) and their ability to enhance differentiation and immunoglobulin production by secreting interleukin 5 (IL-5). Such B-1-cell and ILC2 dysfunction is potentially due to cleavage of p38 and Erk1/2 mitogen-activated protein kinases in these cells. Conversely, mice that survived infection generated neutralizing antibodies via the formation of robust germinal center B cells in Peyer's patches and had restored B-1-cell and ILC2 function. These data may provide additional insight for designing efficacious vaccines and therapeutics against this deadly pathogen.


Asunto(s)
Carbunco/inmunología , Linfocitos B/fisiología , Bacillus anthracis/fisiología , Enfermedades Gastrointestinales/inmunología , Animales , Bacillus anthracis/inmunología , Colon/inmunología , Colon/microbiología , Citometría de Flujo , Inmunidad Celular/inmunología , Ratones , Reacción en Cadena en Tiempo Real de la Polimerasa
6.
Anticancer Drugs ; 24(10): 1098-103, 2013 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-23995854
7.
Cell Immunol ; 270(2): 172-82, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21621198

RESUMEN

Chemokines and their receptors have been studied in several solid tumor models as mediators of inflammation. In turn, inflammation has been implicated in the promotion and progression of tumors, and as such, chemokines have been proposed as novel molecular targets for chemotherapy. While the expression of these molecules has been described in tumor cells, endothelial cells, macrophages and neutrophils, less attention has been paid to the expression profile of these molecules by T lymphocytes in the periphery or infiltrating the tumor. Using the D1-DMBA-3 murine mammary adenocarcinoma model, we aimed to better characterize the differential expression of chemokines and/or their receptors in the host and in the tumor microenvironment, and specifically, in the T cells of tumor-bearing mice compared to normal control animals. We found that T lymphocytes from tumor-bearing mice express the pro-inflammatory chemokines, CCL2, CCL5 and CXCL2, as well as the chemokine receptors, CCR1, CCR2, CCR3 and CXCR2.


Asunto(s)
Quimiocinas/metabolismo , Mediadores de Inflamación/metabolismo , Neoplasias Mamarias Experimentales/inmunología , Receptores de Quimiocina/metabolismo , Linfocitos T/inmunología , Adenocarcinoma/genética , Adenocarcinoma/inmunología , Animales , Línea Celular Tumoral , Quimiocina CCL2/genética , Quimiocina CCL2/metabolismo , Quimiocina CCL2/farmacología , Quimiocina CCL5/genética , Quimiocina CCL5/metabolismo , Quimiocina CXCL2/genética , Quimiocina CXCL2/metabolismo , Quimiocinas/genética , Femenino , Expresión Génica , Linfocitos Infiltrantes de Tumor/inmunología , Neoplasias Mamarias Experimentales/genética , Ratones , Ratones Endogámicos BALB C , ARN Mensajero/genética , ARN Neoplásico/genética , Receptores CCR1/genética , Receptores CCR1/metabolismo , Receptores CCR2/genética , Receptores CCR2/metabolismo , Receptores CCR3/genética , Receptores CCR3/metabolismo , Receptores de Quimiocina/genética , Receptores de Interleucina-8B/genética , Receptores de Interleucina-8B/metabolismo , Proteínas Recombinantes/farmacología , Subgrupos de Linfocitos T/inmunología
8.
Int J Mol Med ; 21(1): 125-34, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18097625

RESUMEN

Matrix metalloproteinases (MMPs) are a family of extracellular proteinases whose contributions to cancer progression have been studied because of their matrix-degrading abilities and elevated expression in advanced stage tumors. Recent findings suggest a role for MMPs during the multiple stages of tumor progression including establishment and growth, migration, invasion, metastasis, and angiogenesis. MMP-9 regulation at the molecular level can be studied by measuring the effect(s) of a variety of physiological and pharmacological agents on cells. Multiple signaling molecules such as protein kinase C, pertussis toxin-sensitive guanine nucleotide-binding protein G, and protein tyrosine kinases are known to mediate the secretion of MMPs in cell lines. We previously reported an upregulation of MMP-9 in T cells of mammary tumor-bearing mice. In this study, pharmacologic inhibitors were used to dissect the signaling pathways involved in the upregulation of MMP-9 in the splenic T cells of normal and mammary tumor-bearing mice. Staurosporine, a protein kinase inhibitor, stimulated MMP-9 secretion by normal T lymphocytes, while the constitutively high levels of MMP-9 produced by tumor bearers' T cells were decreased by Genistein, a specific tyrosine kinase inhibitor, and Rottlerin, a PKC inhibitor. Using a NF-kappaB specific probe to the murine MMP-9 promoter, electromobility shift assays of nuclear proteins from normal and tumor bearers' splenic T cells revealed a pattern of higher intensity bands from the tumor bearers' nuclear extracts, indicating a greater amount of these transcription factors bound to the recognition motif. When mammary tumor bearers' T cells were cultured with the NF-kappaB inhibitors, N-p-Tosyl-L-lysine chloromethyl ketone hydrochloride and Bay 11-7082, there was a subsequent decreased production of MMP-9. These results suggest that the tumor burden may be activating various signaling pathways within splenic T lymphocytes to upregulate MMP-9 expression.


Asunto(s)
Regulación Neoplásica de la Expresión Génica , Neoplasias Mamarias Animales/enzimología , Neoplasias Mamarias Animales/genética , Metaloproteinasa 9 de la Matriz/genética , Linfocitos T/enzimología , Animales , ADN de Neoplasias/metabolismo , Inhibidores Enzimáticos/farmacología , Regulación Enzimológica de la Expresión Génica/efectos de los fármacos , Regulación Neoplásica de la Expresión Génica/efectos de los fármacos , Quinasa I-kappa B/metabolismo , Proteínas I-kappa B/metabolismo , Isoenzimas/antagonistas & inhibidores , Neoplasias Mamarias Animales/patología , Metaloproteinasa 9 de la Matriz/metabolismo , Ratones , Ratones Endogámicos BALB C , FN-kappa B/metabolismo , Fosfotirosina/metabolismo , Regiones Promotoras Genéticas/genética , Unión Proteica/efectos de los fármacos , Proteína Quinasa C/antagonistas & inhibidores , Estabilidad del ARN/efectos de los fármacos , ARN Mensajero/genética , ARN Mensajero/metabolismo , Transducción de Señal/efectos de los fármacos , Linfocitos T/efectos de los fármacos
9.
Vaccine ; 36(1): 155-164, 2018 01 02.
Artículo en Inglés | MEDLINE | ID: mdl-29180028

RESUMEN

Clostridium botulinum readily persists in the soil and secretes life-threatening botulinum neurotoxins (BoNTs) that are categorized into serotypes A to H, of which, serotype A (BoNT/A) is the most commonly occurring in nature. An efficacious vaccine with high longevity against BoNT intoxication is urgent. Herein, we developed a dual-route vaccine administered over four consecutive weeks by mucosal and parenteral routes, consisting of the heavy chain (Hc) of BoNT/A targeting dendritic cell peptide (DCpep) expressed by Lactobacillus acidophilus as a secretory immunogenic protein. The administered dual-route vaccine elicited robust and long-lasting memory B cell responses comprising germinal center (GC) B cells and follicular T cells (Tfh) that fully protected mice from lethal oral BoNT/A fatal intoxication. Additionally, passively transferring neutralizing antibodies against BoNT/A into naïve mice induced robust protection against BoNT/A lethal intoxication. Together, a targeted vaccine employing local and systemic administrative routes may represent a novel formulation eliciting protective B cell responses with remarkable longevity against threatening biologic agents such as BoNTs.


Asunto(s)
Anticuerpos Neutralizantes/inmunología , Vacunas Bacterianas/inmunología , Toxinas Botulínicas Tipo A/inmunología , Neurotoxinas/inmunología , Vacunación/métodos , Administración a través de la Mucosa , Animales , Anticuerpos Antibacterianos/inmunología , Anticuerpos Neutralizantes/administración & dosificación , Linfocitos B/inmunología , Vacunas Bacterianas/administración & dosificación , Botulismo/prevención & control , Clostridium botulinum/inmunología , Células Dendríticas/química , Células Dendríticas/inmunología , Vías de Administración de Medicamentos , Inmunización Pasiva , Memoria Inmunológica , Lactobacillus acidophilus/química , Ratones , Péptidos/administración & dosificación , Péptidos/genética , Péptidos/inmunología , Péptidos/metabolismo , Serogrupo
11.
Int J Mol Med ; 20(1): 129-36, 2007 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-17549399

RESUMEN

MCP-1/CCL2 (monocyte chemoattractant protein-1/CC chemokine ligand 2) is a beta or CC chemokine that is expressed by a variety of cell types, including fibroblasts, endothelial, smooth muscle, and glial cells. In addition, cells involved in immunity, such as monocytes/macrophages, neutrophils, and eosinophils have also been shown to express this chemoattractant. Using a murine model of the D1-DMBA-3 mammary adenocarcinoma, we demonstrated the unique production of CCL2 by splenic T lymphocytes from tumor-bearing animals. Because this tumor produces GM-CSF, and this factor is also up-regulated in the B lymphocytes of tumor-bearing mice, we looked at the ability of GM-CSF to induce CCL2 production by T cells. Treatment of normal and tumor bearers' T cells with GM-CSF resulted in an increased secretion of this chemokine. This up-regulation was seen with or without stimulation by Concanavalin A, although these treatments were additive in their effects. The induction of CCL2 was studied at the molecular level by analyzing the effect(s) of a variety of physiological and pharmacological agents on cultured T cells. These results suggest that the tumor-derived factor GM-CSF activates various signaling pathways within splenic T cells to up-regulate CCL2 expression.


Asunto(s)
Quimiocina CCL2/metabolismo , Regulación Neoplásica de la Expresión Génica , Factor Estimulante de Colonias de Granulocitos y Macrófagos/farmacología , Neoplasias Mamarias Experimentales/metabolismo , Linfocitos T/metabolismo , Animales , Células Cultivadas , Factor Estimulante de Colonias de Granulocitos y Macrófagos/genética , Neoplasias Mamarias Experimentales/inducido químicamente , Ratones , Ratones Endogámicos BALB C , ARN Mensajero/análisis , Proteínas Recombinantes , Bazo/citología , Linfocitos T/efectos de los fármacos , Regulación hacia Arriba/efectos de los fármacos
12.
Cancer Res ; 65(22): 10578-84, 2005 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-16288051

RESUMEN

Interactions between malignant tumors and the host immune system shape the course of cancer progression. The molecular basis of such interactions is the subject of immense interest. Proinflammatory cytokines produced by macrophages are critical mediators of immune responses that contribute to the control of the advancement of neoplasia. We have shown that the expressions of interleukin 12 (IL-12) and inducible nitric oxide synthase (iNOS) are decreased in macrophages from mammary tumor-bearing mice. In this study, we investigated the causes of IL-12 dysregulation and found deficient nuclear factor kappaB (NFkappaB) and CCAAT/enhancer binding protein (C/EBP) expression and function in tumor bearers' peritoneal macrophages. The constitutive expressions of NFkappaB p50, c-rel, p65, and C/EBPalpha and beta, as well as the lipopolysaccharide-induced nuclear translocation and DNA binding of NFkappaB components and C/EBPalpha and beta, are profoundly impaired in macrophages from mice bearing D1-DMBA-3 tumors. Because similar findings occur with the iNOS gene, it seems that it represents a novel mechanism by which tumor-derived factors interfere with the host immune defenses.


Asunto(s)
Proteínas Potenciadoras de Unión a CCAAT/inmunología , Macrófagos Peritoneales/inmunología , Neoplasias Mamarias Experimentales/inmunología , FN-kappa B/inmunología , Animales , Proteínas Potenciadoras de Unión a CCAAT/biosíntesis , Proteínas Potenciadoras de Unión a CCAAT/deficiencia , Proteínas Potenciadoras de Unión a CCAAT/genética , Núcleo Celular/metabolismo , Femenino , Proteínas I-kappa B/metabolismo , Interleucina-12/biosíntesis , Macrófagos Peritoneales/metabolismo , Masculino , Neoplasias Mamarias Experimentales/genética , Ratones , Ratones Endogámicos BALB C , Inhibidor NF-kappaB alfa , FN-kappa B/biosíntesis , FN-kappa B/deficiencia , FN-kappa B/genética , Fosforilación , Regiones Promotoras Genéticas , ARN Mensajero/biosíntesis , ARN Mensajero/genética
13.
J Clin Invest ; 127(11): 3970-3986, 2017 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-28945202

RESUMEN

Consumption of human breast milk (HBM) attenuates the incidence of necrotizing enterocolitis (NEC), which remains a leading and intractable cause of mortality in preterm infants. Here, we report that this diminution correlates with alterations in the gut microbiota, particularly enrichment of Propionibacterium species. Transfaunation of microbiota from HBM-fed preterm infants or a newly identified and cultured Propionibacterium strain, P. UF1, to germfree mice conferred protection against pathogen infection and correlated with profound increases in intestinal Th17 cells. The induction of Th17 cells was dependent on bacterial dihydrolipoamide acetyltransferase (DlaT), a major protein expressed on the P. UF1 surface layer (S-layer). Binding of P. UF1 to its cognate receptor, SIGNR1, on dendritic cells resulted in the regulation of intestinal phagocytes. Importantly, transfer of P. UF1 profoundly mitigated induced NEC-like injury in neonatal mice. Together, these results mechanistically elucidate the protective effects of HBM and P. UF1-induced immunoregulation, which safeguard against proinflammatory diseases, including NEC.


Asunto(s)
Propionibacterium/inmunología , Células Th17/fisiología , Animales , Proteínas Bacterianas/fisiología , Diferenciación Celular , Colon/inmunología , Colon/microbiología , Acetiltransferasa de Residuos Dihidrolipoil-Lisina/fisiología , Femenino , Microbioma Gastrointestinal , Genoma Bacteriano , Humanos , Inmunomodulación , Recién Nacido , Recien Nacido Prematuro , Ratones de la Cepa 129 , Ratones Endogámicos BALB C , Ratones Endogámicos C57BL , Anotación de Secuencia Molecular , Propionibacterium/enzimología , Propionibacterium/genética , Análisis de Secuencia de ADN
14.
Front Physiol ; 8: 220, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28446880

RESUMEN

The brain-gut axis plays a critical role in the regulation of different diseases, many of which are characterized by sympathetic dysregulation. However, a direct link between sympathetic dysregulation and gut dysbiosis remains to be illustrated. Bone marrow (BM)-derived immune cells continuously interact with the gut microbiota to maintain homeostasis in the host. Their function is largely dependent upon the sympathetic nervous system acting via adrenergic receptors present on the BM immune cells. In this study, we utilized a novel chimera mouse that lacks the expression of BM beta1/2 adrenergic receptors (b1/2-ARs) to investigate the role of the sympathetic drive to the BM in gut and microbiota homeostasis. Fecal analyses demonstrated a shift from a dominance of Firmicutes to Bacteroidetes phylum in the b1/2-ARs KO chimera, resulting in a reduction in Firmicutes/Bacteroidetes ratio. Meanwhile, a significant reduction in Proteobacteria phylum was determined. No changes in the abundance of acetate-, butyrate-, and lactate-producing bacteria, and colon pathology were observed in the b1/2-ARs KO chimera. Transcriptomic profiling in colon identified Killer Cell Lectin-Like Receptor Subfamily D, Member 1 (Klrd1), Membrane-Spanning 4-Domains Subfamily A Member 4A (Ms4a4b), and Casein Kinase 2 Alpha Prime Polypeptide (Csnk2a2) as main transcripts associated with the microbiota shifts in the b1/2-ARs KO chimera. Suppression of leukocyte-related transcriptome networks (i.e., function, differentiation, migration), classical compliment pathway, and networks associated with intestinal function, barrier integrity, and excretion was also observed in the colon of the KO chimera. Moreover, reduced expression of transcriptional networks related to intestinal diseases (i.e., ileitis, enteritis, inflammatory lesions, and stress) was noted. The observed suppressed transcriptome networks were associated with a reduction in NK cells, macrophages, and CD4+ T cells in the b1/2-ARs KO chimera colon. Thus, sympathetic regulation of BM-derived immune cells plays a significant role in modifying inflammatory networks in the colon and the gut microbiota composition. To our knowledge, this study is the first to suggest a key role of BM b1/2-ARs signaling in host-microbiota interactions, and reveals specific molecular mechanisms that may lead to generation of novel anti-inflammatory treatments for many immune and autonomic diseases as well as gut dysbiosis across the board.

15.
Vaccine ; 34(12): 1480-8, 2016 Mar 14.
Artículo en Inglés | MEDLINE | ID: mdl-26802606

RESUMEN

The importance of vaccine-induced T-cell immunity in conferring protection with prototype and commercial FIV vaccines is still unclear. Current studies performed adoptive transfer of T cells from prototype FIV-vaccinated cats to partial-to-complete feline leukocyte antigen (FLA)-matched cats a day before either homologous FIVPet or heterologous-subtype pathogenic FIVFC1 challenge. Adoptive-transfer (A-T) conferred a protection rate of 87% (13 of 15, p < 0.001) against FIVPet using the FLA-matched T cells, whereas all 12 control cats were unprotected. Furthermore, A-T conferred protection rate of 50% (6 of 12, p<0.023) against FIVFC1 using FLA-matched T cells, whereas all 8 control cats were unprotected. Transfer of FLA-matched T and B cells demonstrated that T cells are needed to confer A-T protection. In addition, complete FLA-matching and addition of T-cell numbers > 13 × 10(6) cells were required for A-T protection against FIVFC1 strain, reported to be a highly pathogenic virus resistant to vaccine-induced neutralizing-antibodies. The addition of FLA-matched B cells alone was not protective. The poor quality of the anti-FIV T-cell immunity induced by the vaccine likely contributed to the lack of protection in an FLA-matched recipient against FIVFC1. The quality of the immune response was determined by the presence of high mRNA levels of cytolysin (perforin) and cytotoxins (granzymes A, B, and H) and T helper-1 cytokines (interferon-γ [IFNγ] and IL2). Increased cytokine, cytolysin and cytotoxin production was detected in the donors which conferred protection in A-T studies. In addition, the CD4(+) and CD8(+) T-cell proliferation and/or IFNγ responses to FIV p24 and reverse transcriptase increased with each year in cats receiving 1X-3X vaccine boosts over 4 years. These studies demonstrate that anti-FIV T-cell immunity induced by vaccination with a dual-subtype FIV vaccine is essential for prophylactic protection against AIDS lentiviruses such as FIV and potentially HIV-1.


Asunto(s)
Traslado Adoptivo , Síndrome de Inmunodeficiencia Adquirida del Felino/inmunología , Inmunidad Celular , Linfocitos T/inmunología , Vacunación/veterinaria , Vacunas Virales/inmunología , Animales , Anticuerpos Neutralizantes/sangre , Anticuerpos Antivirales/sangre , Linfocitos B/inmunología , Gatos , Síndrome de Inmunodeficiencia Adquirida del Felino/prevención & control , Antígenos de Histocompatibilidad Clase I/inmunología , Virus de la Inmunodeficiencia Felina , Interferón gamma/inmunología , Interleucina-2/inmunología
16.
Trends Mol Med ; 21(3): 154-63, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-25577136

RESUMEN

Bacterial infections are the primary cause of gastrointestinal (GI) disorders in both developing and developed countries, and are particularly dangerous for infants and children. Bacillus anthracis is the 'archetype zoonotic' pathogen; no other infectious disease affects such a broad range of species, including humans. Importantly, there are more case reports of GI anthrax infection in children than inhalational disease. Early diagnosis is difficult and widespread systemic disease develops rapidly. This review highlights new findings concerning the roles of the gut epithelia, commensal microbiota, and innate lymphoid cells (ILCs) in initiation of disease and systemic dissemination in animal models of GI anthrax, the understanding of which is crucial to designing alternative therapies that target the establishment of infection.


Asunto(s)
Carbunco/microbiología , Carbunco/patología , Bacillus anthracis/fisiología , Enfermedades Gastrointestinales/microbiología , Enfermedades Gastrointestinales/patología , Animales , Carbunco/inmunología , Linfocitos B/inmunología , Modelos Animales de Enfermedad , Epitelio/patología , Enfermedades Gastrointestinales/inmunología , Microbioma Gastrointestinal , Humanos
17.
Toxins (Basel) ; 7(9): 3805-17, 2015 Sep 22.
Artículo en Inglés | MEDLINE | ID: mdl-26402706

RESUMEN

Ingestion of Bacillus anthracis results in rapid gastrointestinal (GI) infection, known as GI anthrax. We previously showed that during GI anthrax, there is swift deterioration of intestinal barrier function leading to translocation of gut-associated bacteria into systemic circulation. Additionally, we described dysfunction in colonic B cells. In concordance with our previous studies, here, we report early migration of the Sterne strain of B. anthracis along with other gut-resident bacteria into the infected murine liver. Additionally, despite a global decrease in the B cell population, we observed an increase in both B-1a and marginal zone (MZ)-like B cells. Both of these cell types are capable of producing immunoglobulins against common pathogens and commensals, which act as a general antibody barrier before an antigen-specific antibody response. Accumulation of these cells in the liver was associated with an increase in chemokine expression. These data suggest that the presence of Sterne and other commensals in the liver trigger migration of MZ-like B cells from the spleen to the liver to neutralize systemic spread. Further research is required to evaluate the possible cause of their failure to clear the infection within the liver, including the potential role of dysfunctional mitogen-activated protein kinase (MAPK) signaling.


Asunto(s)
Carbunco/microbiología , Linfocitos B/microbiología , Bacillus anthracis/metabolismo , Enfermedades Gastrointestinales/microbiología , Tracto Gastrointestinal/microbiología , Animales , Carbunco/patología , Linfocitos B/metabolismo , Colon/microbiología , Modelos Animales de Enfermedad , Enfermedades Gastrointestinales/patología , Tracto Gastrointestinal/patología , Hígado/microbiología , Ratones , Bazo/microbiología , Esporas Bacterianas/metabolismo
18.
Gut Microbes ; 6(6): 392-7, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26647142

RESUMEN

Intestinal immunity is subject to complex and fine-tuned regulation dictated by interactions of the resident microbial community and their gene products with host innate cells. Deterioration of this delicate process may result in devastating autoinflammatory diseases, including inflammatory bowel disease (IBD), which primarily comprises Crohn's disease (CD) and ulcerative colitis (UC). Efficacious interventions to regulate proinflammatory signals, which play critical roles in IBD, require further scientific investigation. We recently demonstrated that rebalancing intestinal immunity via the surface layer protein A (SlpA) from Lactobacillus acidophilus NCFM potentially represents a feasible therapeutic approach to restore intestinal homeostasis. To expand on these findings, we established a new method of purifying bacterial SlpA, a new SlpA-specific monoclonal antibody, and found no SlpA-associated toxicity in mice. Thus, these data may assist in our efforts to determine the immune regulatory efficacy of SlpA in humans.


Asunto(s)
Proteínas Bacterianas/uso terapéutico , Terapia Biológica , Enfermedades Intestinales/terapia , Lactobacillus acidophilus , Secuencia de Aminoácidos , Animales , Anticuerpos Antibacterianos/inmunología , Anticuerpos Monoclonales/inmunología , Proteínas Bacterianas/inmunología , Proteínas Bacterianas/aislamiento & purificación , Proteínas Bacterianas/toxicidad , Microbioma Gastrointestinal , Homeostasis , Intestinos/microbiología , Lactobacillus acidophilus/química , Lactobacillus acidophilus/inmunología , Ratones , Ratones Endogámicos C57BL , Datos de Secuencia Molecular
19.
Breast Dis ; 20: 145-53, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15687715

RESUMEN

It has been reported that in epithelial cancer invasion, most matrix metalloproteinases (MMPs) are made by stromal cells of the host, and not the neoplasm itself. Findings from several laboratories indicate that immune cell-derived MMPs may be advantageous to developing tumors by promoting angiogenesis, neoplastic cell proliferation, and progression to malignancy. We have found a dramatic up-regulation of MMP-9 secretion by splenic and tumor-infiltrating T lymphocytes from D1-DMBA-3 mammary tumor-bearing mice compared to T cells from normal animals. Furthermore, tumor-derived vascular endothelial growth factor induced the up-regulation of MMP-9 in T cells, corroborating the suggestion that tumor cells may "conscript" inflammatory cells to make contributions to the tumor phenotype. Some investigators propose that the resulting degradation of the extracellular matrix by lymphocyte-derived proteases might be used by tumor cells to establish a blood supply and to metastasize. The outcome of MMP activity in the tumor microenvironment may be dependent on a variety of factors including tumor phenotype; the presence of other proteases and cytokines; and the time, level, and site of MMP production. In light of recent findings that MMPs are also capable of generating anti-angiogenic molecules, further investigation will bear out whether inflammatory cell-derived MMPs are friend or foe to developing tumors.


Asunto(s)
Neoplasias de la Mama/inmunología , Neoplasias de la Mama/metabolismo , Metaloproteinasa 9 de la Matriz/metabolismo , Linfocitos T/inmunología , Animales , Humanos
20.
PLoS One ; 9(6): e100532, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24945934

RESUMEN

Gastrointestinal (GI) anthrax results from the ingestion of Bacillus anthracis. Herein, we investigated the pathogenesis of GI anthrax in animals orally infected with toxigenic non-encapsulated B. anthracis Sterne strain (pXO1+ pXO2-) spores that resulted in rapid animal death. B. anthracis Sterne induced significant breakdown of intestinal barrier function and led to gut dysbiosis, resulting in systemic dissemination of not only B. anthracis, but also of commensals. Disease progression significantly correlated with the deterioration of innate and T cell functions. Our studies provide critical immunologic and physiologic insights into the pathogenesis of GI anthrax infection, whereupon cleavage of mitogen-activated protein kinases (MAPKs) in immune cells may play a central role in promoting dysfunctional immune responses against this deadly pathogen.


Asunto(s)
Carbunco/inmunología , Carbunco/microbiología , Bacillus anthracis/inmunología , Colon/inmunología , Disbiosis/inmunología , Disbiosis/microbiología , Enfermedades Gastrointestinales/inmunología , Enfermedades Gastrointestinales/microbiología , Tolerancia Inmunológica , Animales , Carbunco/enzimología , Carbunco/patología , Colon/microbiología , Colon/patología , Disbiosis/patología , Epitelio/inmunología , Epitelio/microbiología , Epitelio/patología , Enfermedades Gastrointestinales/enzimología , Enfermedades Gastrointestinales/patología , Inmunidad Innata , Ratones , Proteínas Quinasas Activadas por Mitógenos/metabolismo , Linfocitos T/inmunología
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