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1.
Front Pharmacol ; 9: 179, 2018.
Article in English | MEDLINE | ID: mdl-29559912

ABSTRACT

Inflammatory bowel disease (IBD) is a group of chronic inflammatory conditions of the gastrointestinal tract characterized by an exacerbated mucosal immune response. Macrophages play pivotal roles in the maintenance of gut homeostasis but they are also implicated in the pathogenesis of IBD. They are highly plastic cells and their activation state depends on the local environment. In the healthy intestine, resident macrophages display an M2 phenotype characterized by inflammatory energy, while inflammatory M1 macrophages dominate in the inflamed intestinal mucosa. In this regard, modifying the balance of macrophage populations into an M2 phenotype has emerged as a new therapeutic approach in IBD. Multipotent mesenchymal stromal cells (MSCs) have been proposed as a promising cell-therapy for the treatment of IBD, considering their immunomodulatory and tissue regenerative potential. Numerous preclinical studies have shown that MSCs can induce immunomodulatory macrophages and have demonstrated that their therapeutic efficacy in experimental colitis is mediated by macrophages with an M2-like phenotype. However, some issues have not been clarified yet, including the importance of MSC homing to the inflamed colon and/or lymphoid organs, their optimal route of administration or whether they are effective as living or dead cells. In contrast, the mechanisms behind the effect of MSCs in human IBD are not known and more data are needed regarding the effect of MSCs on macrophage polarization that would support the observation reported in the experimental models. Nevertheless, MSCs have emerged as a novel method to treat IBD that has already been proven safe and with clinical benefits that could be administered in combination with the currently used pharmacological treatments.

2.
Eur J Immunol ; 36(6): 1374-85, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16708405

ABSTRACT

Repetitive antigen stimulation induces peripheral T cell tolerance in vivo. It is not known, however, whether multiple stimulations merely suppress T cell activation or, alternatively, change the transcriptional program to a distinct, tolerant state. In this study, we have discovered that STAT3 and STAT5 were activated in response to antigen stimulation in vivo, in marked contrast to the suppression of AP-1, NF-kappaB and NFAT. In addition, a number of transcription factors were induced in tolerant T cells following antigen challenge in vivo, including T-bet, Irf-1 and Egr-2. The altered transcription program in tolerant cells associates closely with the suppression of cell cycle progression and IL-2 production, as well as with the induction of IL-10. Studies of T-bet and Egr-2 show that the function of T-bet in peptide treatment-induced regulatory T cells is not associated with Th1 differentiation, but correlates with the suppression of IL-2, whereas expression of Egr-2 led to an up-regulation of the cell cycle inhibitors p21(cip1) and p27(kip). Our results demonstrate a balanced transcription program regulated by different transcription factors for T cell activation and/or tolerance during antigen-induced T cell responses. Persistent antigen stimulation can induce T cell tolerance by changing the balance of transcription factors.


Subject(s)
Epitopes, T-Lymphocyte/immunology , T-Lymphocytes, Regulatory/immunology , Transcription, Genetic/immunology , Animals , Cell Cycle/immunology , Cell Nucleus/immunology , Cell Nucleus/metabolism , Cyclin-Dependent Kinase Inhibitor p21/biosynthesis , Cyclin-Dependent Kinase Inhibitor p21/genetics , Cyclin-Dependent Kinase Inhibitor p21/immunology , Cyclin-Dependent Kinase Inhibitor p27/biosynthesis , Cyclin-Dependent Kinase Inhibitor p27/genetics , Cyclin-Dependent Kinase Inhibitor p27/immunology , Early Growth Response Protein 2/biosynthesis , Early Growth Response Protein 2/genetics , Early Growth Response Protein 2/immunology , Gene Expression Profiling , Gene Expression Regulation/immunology , Immune Tolerance/immunology , Interleukin-2/biosynthesis , Interleukin-2/immunology , Lymphocyte Activation/immunology , Mice , Mice, Transgenic , Oligonucleotide Array Sequence Analysis , RNA/chemistry , RNA/genetics , Reverse Transcriptase Polymerase Chain Reaction , Signal Transduction/immunology , T-Box Domain Proteins , Transcription Factors/genetics , Transcription Factors/immunology , Transcription Factors/metabolism , Transfection
3.
J Immunol ; 174(1): 310-9, 2005 Jan 01.
Article in English | MEDLINE | ID: mdl-15611254

ABSTRACT

Intranasal administration of peptide Ac1-9[4Y], based on the N-terminal epitope of myelin basic protein, can induce CD4(+) T cell tolerance, and suppress experimental autoimmune encephalomyelitis induction. The peptide-induced regulatory T (PI-T(Reg)) cells failed to produce IL-2, but expressed IL-10 in response to Ag and could suppress naive T cell responses in vitro. Analysis of Jak-STAT signaling pathways revealed that the activation of Jak1, STAT3, and STAT5 were induced in tolerant T cells after Ag stimulation in vivo. In addition, the expression of suppressor of cytokine signaling 3 was induced in tolerant T cells, suggesting that cytokines regulate the tolerant state of the PI-T(Reg) cells. Stimulation of PI-T(Reg) cells in vitro with IL-10 induced Jak1 and STAT3 activation, but not STAT5, suggesting that IL-10 is important, but not the only cytokine involved in the development of T cell tolerance. Although IL-2 expression was deficient, stimulation with IL-2 in vitro induced Jak1 and STAT5 activation in PI-T(Reg) cells, restored their proliferative response to antigenic stimulation, and abrogated PI-T(Reg)-mediated suppression in vitro. However, the addition of IL-2 could not suppress IL-10 expression, and the IL-2 gene remained inactive. After withdrawal of IL-2, the PI-T(Reg) cells regained their nonproliferative state and suppressive ability. These results underline the ability of the immune system to maintain tolerance to autoantigens, but at the same time having the ability to overcome the suppressive phenotype of tolerant T cells by cytokines, such as IL-2, during the protective immune response to infection.


Subject(s)
Immune Tolerance , Interleukin-10/immunology , Interleukin-2/immunology , Signal Transduction/immunology , T-Lymphocytes/immunology , Animals , Autoantigens/immunology , Blotting, Western , Cells, Cultured , Cytokines/biosynthesis , Cytokines/immunology , DNA-Binding Proteins/immunology , Electrophoresis, Polyacrylamide Gel , Janus Kinase 1 , Mice , Myelin Basic Protein/administration & dosage , Myelin Basic Protein/immunology , Peptides/administration & dosage , Peptides/immunology , Protein-Tyrosine Kinases/immunology , RNA, Messenger/analysis , Reverse Transcriptase Polymerase Chain Reaction , STAT1 Transcription Factor , Trans-Activators/immunology , Transcription Factors/biosynthesis , Transcription Factors/immunology , Transforming Growth Factor beta/immunology
4.
J Biol Chem ; 279(33): 34107-14, 2004 Aug 13.
Article in English | MEDLINE | ID: mdl-15123678

ABSTRACT

The suppressors of cytokine signaling (SOCS) family is thought to act largely as a negative regulator of signaling by cytokines and some growth factors. Surprisingly, the SOCS-6 transgenics had no significant defects in the cytokine signaling and hematopoietic system but displayed significant improvements in glucose metabolism. Insulin stimulation of Akt/protein kinase B was also potentiated. Biochemical analysis showed that, after insulin stimulation, SOCS-6 interacted with the monomeric p85 subunit of class-Ia phosphoinositide (PI) 3-kinase but not with p85/p110 dimers. Furthermore, SOCS-6 expression is transiently increased by serum and insulin in normal fibroblasts. However, both the mRNA and protein of SOCS-6 were rapidly degraded after induction by insulin. The degradation of the SOCS-6 protein was partially inhibited by a proteasome inhibitor, suggesting a proteasome-mediated degradation mechanism. In contrast, SOCS-6-associated p85 was not degraded and could be recruited to the newly synthesized SOCS-6 molecules in the presence of insulin, suggesting that SOCS-6 expression and its interaction with p85, but not the degradation, is regulated by insulin. The phenotype of SOCS-6 transgenic mice bears a striking resemblance to p85 knock-out mouse models in which glucose metabolism stimulated by insulin is significantly improved despite reduced activation of PI 3-kinase. This suggests that monomeric p85 might play a physiologically important role in attenuating signaling through PI 3-kinase-dependent pathways in unstimulated cells. Therefore, our results indicate that SOCS-6 may provide a dynamically regulated mechanism by which insulin can transiently overcome the negative effects that p85 monomers have on signaling via PI 3-kinase-dependent signaling pathways.


Subject(s)
Gene Expression Regulation, Enzymologic , Glucose/metabolism , Insulin/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Protein Biosynthesis , Proteins , Animals , Blood Glucose/metabolism , Blotting, Northern , CHO Cells , Cell Division , Cells, Cultured , Cricetinae , Cysteine Endopeptidases/metabolism , Electrophoresis, Polyacrylamide Gel , Fibroblasts/metabolism , Mice , Mice, Inbred C57BL , Mice, Transgenic , Multienzyme Complexes/metabolism , Myocytes, Cardiac/metabolism , Nuclear Proteins/metabolism , Phenotype , Proteasome Endopeptidase Complex , Protein Serine-Threonine Kinases/metabolism , Protein Structure, Tertiary , Proto-Oncogene Proteins/metabolism , Proto-Oncogene Proteins c-akt , Signal Transduction , Suppressor of Cytokine Signaling Proteins , Time Factors , Transfection , Transgenes
5.
Int Immunol ; 15(3): 403-9, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12618484

ABSTRACT

TCR signaling is mediated by intracellular signaling molecules and nuclear transcription factors, which are tightly regulated by interaction with regulatory proteins such as Grb2 and SLAP. We reported recently that TCR stimulation induces the expression of cytokine-induced SH2 protein (CIS). The expression of CIS promotes TCR-mediated activation. We have now found specific interactions between CIS and activated protein kinase C (PKC) alpha, beta and theta in TCR-stimulated T cells. CIS was shown by in vitro kinase assay to associate with activated PKC. In CIS-expressing T cells isolated from CIS-transgenic mice, the amount of activated PKC associated with CIS was found to increase following TCR stimulation. By immunohistochemical analysis, CIS was also found to co-localize with PKCtheta at the plasma membrane of activated T cells. In addition to the interaction and intracellular co-localization of the CIS and PKC, an increase in the activation of AP-1 and NF-kappaB was noted in CIS-expressing T cells, after stimulation by either anti-CD3/CD28 or phorbol myristate acetate + ionomycin. These results suggest that CIS regulates PKC activation, and that this may be important for the activation of both the AP-1 and NF-kappaB pathways in TCR signaling.


Subject(s)
Immediate-Early Proteins/physiology , Protein Kinase C/physiology , T-Lymphocytes/physiology , Animals , CD28 Antigens/immunology , CD3 Complex/immunology , Cytokines/physiology , Mice , NF-kappa B/metabolism , Receptors, Antigen, T-Cell/physiology , Suppressor of Cytokine Signaling Proteins , T-Lymphocytes/immunology , Transcription Factor AP-1/metabolism , src Homology Domains/physiology
6.
J Biol Chem ; 277(21): 18266-71, 2002 May 24.
Article in English | MEDLINE | ID: mdl-11884415

ABSTRACT

Tapasin is a subunit of the transporter associated with antigen processing (TAP). It associates with the major histocompatibility complex (MHC) class I. We show that tapasin interacts with beta- and gamma-subunits of COPI coatomer. COPI retrieves membrane proteins from the Golgi network back to the endoplasmic reticulum (ER). The COPI subunit-associated tapasin also interacts with MHC class I molecules suggesting that tapasin acts as the cargo receptor for packing MHC class I molecules as cargo proteins into COPI-coated vesicles. In tapasin mutant cells, neither TAP nor MHC class I are detected in association with the COPI coatomer. Interestingly, tapasin-associated MHC class I molecules are antigenic peptide-receptive and detected in both the ER and the Golgi. Our data suggest that tapasin is required for the COPI vesicle-mediated retrograde transport of immature MHC class I molecules from the Golgi network to the ER.


Subject(s)
Antiporters/metabolism , Coat Protein Complex I/metabolism , Endoplasmic Reticulum/metabolism , Golgi Apparatus/metabolism , Histocompatibility Antigens Class I/metabolism , Immunoglobulins/metabolism , Biological Transport , Cell Line , Membrane Transport Proteins , Subcellular Fractions/metabolism
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