Role of leptin as an immunomodulator of blood mononuclear cells: mechanisms of action

SUMMARY Leptin is a an adipocyte‐secreted hormone that regulates weight centrally. However, the leptin receptor is expressed not only in the central nervous system, but also in peripheral tissues, such as haematopoietic and immune systems. Therefore, the physiological role of leptin should not be li...

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Veröffentlicht in:Clinical and experimental immunology 2003-07, Vol.133 (1), p.11-19
Hauptverfasser: SÁNCHEZ‐MARGALET, V., MARTÍN‐ROMERO, C., SANTOS‐ALVAREZ, J., GOBERNA, R., NAJIB, S., GONZALEZ‐YANES, C.
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container_title Clinical and experimental immunology
container_volume 133
creator SÁNCHEZ‐MARGALET, V.
MARTÍN‐ROMERO, C.
SANTOS‐ALVAREZ, J.
GOBERNA, R.
NAJIB, S.
GONZALEZ‐YANES, C.
description SUMMARY Leptin is a an adipocyte‐secreted hormone that regulates weight centrally. However, the leptin receptor is expressed not only in the central nervous system, but also in peripheral tissues, such as haematopoietic and immune systems. Therefore, the physiological role of leptin should not be limited to the regulation of food intake and energy expenditure. Moreover, the leptin receptor bears homology to members of the class I cytokine family, and recent data have demonstrated that leptin is able to modulate the immune response. Thus, the leptin receptor is expressed in human peripheral blood mononuclear cells, mediating the leptin effect on proliferation and activation. In vitro activation and HIV infection in vivo induce the expression of the long isoform of the leptin receptor in mononuclear cells. Also, leptin stimulates the production of proinflammatory cytokines from cultured monocytes and enhances the production of Th1 type cytokines from stimulated lymphocytes. Moreover, leptin has a trophic effect on monocytes, preventing apoptosis induced by serum deprivation. Leptin stimulation activates JAK–STAT, IRS‐1‐PI3K and MAPK signalling pathways. Leptin also stimulates Tyr‐phosphorylation of the RNA‐binding protein Sam68 mediating the dissociation from RNA. In this way, leptin signalling could modulate RNA metabolism. These signal transduction pathways provide possible mechanisms whereby leptin may modulate activation of peripheral blood mononuclear cells. Therefore, these data support the hypothesis regarding leptin as a proinflammatory cytokine with a possible role as a link between the nutritional status and the immune response. Moreover, these immunoregulatory functions of leptin could have some relevance in the pathophysiology of obesity.
doi_str_mv 10.1046/j.1365-2249.2003.02190.x
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However, the leptin receptor is expressed not only in the central nervous system, but also in peripheral tissues, such as haematopoietic and immune systems. Therefore, the physiological role of leptin should not be limited to the regulation of food intake and energy expenditure. Moreover, the leptin receptor bears homology to members of the class I cytokine family, and recent data have demonstrated that leptin is able to modulate the immune response. Thus, the leptin receptor is expressed in human peripheral blood mononuclear cells, mediating the leptin effect on proliferation and activation. In vitro activation and HIV infection in vivo induce the expression of the long isoform of the leptin receptor in mononuclear cells. Also, leptin stimulates the production of proinflammatory cytokines from cultured monocytes and enhances the production of Th1 type cytokines from stimulated lymphocytes. Moreover, leptin has a trophic effect on monocytes, preventing apoptosis induced by serum deprivation. Leptin stimulation activates JAK–STAT, IRS‐1‐PI3K and MAPK signalling pathways. Leptin also stimulates Tyr‐phosphorylation of the RNA‐binding protein Sam68 mediating the dissociation from RNA. In this way, leptin signalling could modulate RNA metabolism. These signal transduction pathways provide possible mechanisms whereby leptin may modulate activation of peripheral blood mononuclear cells. Therefore, these data support the hypothesis regarding leptin as a proinflammatory cytokine with a possible role as a link between the nutritional status and the immune response. 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Psychology ; Fundamental immunology ; Humans ; Immunobiology ; Janus Kinase 1 ; leptin ; Leptin - immunology ; Leptin - pharmacology ; leptin receptor ; Leukocytes, Mononuclear - drug effects ; Leukocytes, Mononuclear - immunology ; Lymphocyte Activation ; lymphocytes ; MAP Kinase Signaling System ; Medical sciences ; Metabolic diseases ; Modulation of the immune response (stimulation, suppression) ; Nutritional Status ; Obesity ; Obesity - immunology ; PBMC ; Phosphatidylinositol 3-Kinases - metabolism ; Protein Isoforms - metabolism ; Protein-Tyrosine Kinases - metabolism ; Receptors, Cell Surface - metabolism ; Receptors, Leptin ; Reviews ; Signal Transduction - physiology ; Th1 Cells - metabolism ; Th1 response</subject><ispartof>Clinical and experimental immunology, 2003-07, Vol.133 (1), p.11-19</ispartof><rights>2003 INIST-CNRS</rights><rights>Copyright Blackwell Scientific Publications Ltd. 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However, the leptin receptor is expressed not only in the central nervous system, but also in peripheral tissues, such as haematopoietic and immune systems. Therefore, the physiological role of leptin should not be limited to the regulation of food intake and energy expenditure. Moreover, the leptin receptor bears homology to members of the class I cytokine family, and recent data have demonstrated that leptin is able to modulate the immune response. Thus, the leptin receptor is expressed in human peripheral blood mononuclear cells, mediating the leptin effect on proliferation and activation. In vitro activation and HIV infection in vivo induce the expression of the long isoform of the leptin receptor in mononuclear cells. Also, leptin stimulates the production of proinflammatory cytokines from cultured monocytes and enhances the production of Th1 type cytokines from stimulated lymphocytes. Moreover, leptin has a trophic effect on monocytes, preventing apoptosis induced by serum deprivation. Leptin stimulation activates JAK–STAT, IRS‐1‐PI3K and MAPK signalling pathways. Leptin also stimulates Tyr‐phosphorylation of the RNA‐binding protein Sam68 mediating the dissociation from RNA. In this way, leptin signalling could modulate RNA metabolism. These signal transduction pathways provide possible mechanisms whereby leptin may modulate activation of peripheral blood mononuclear cells. Therefore, these data support the hypothesis regarding leptin as a proinflammatory cytokine with a possible role as a link between the nutritional status and the immune response. 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Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Immunobiology</subject><subject>Janus Kinase 1</subject><subject>leptin</subject><subject>Leptin - immunology</subject><subject>Leptin - pharmacology</subject><subject>leptin receptor</subject><subject>Leukocytes, Mononuclear - drug effects</subject><subject>Leukocytes, Mononuclear - immunology</subject><subject>Lymphocyte Activation</subject><subject>lymphocytes</subject><subject>MAP Kinase Signaling System</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Modulation of the immune response (stimulation, suppression)</subject><subject>Nutritional Status</subject><subject>Obesity</subject><subject>Obesity - immunology</subject><subject>PBMC</subject><subject>Phosphatidylinositol 3-Kinases - metabolism</subject><subject>Protein Isoforms - metabolism</subject><subject>Protein-Tyrosine Kinases - metabolism</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Receptors, Leptin</subject><subject>Reviews</subject><subject>Signal Transduction - physiology</subject><subject>Th1 Cells - metabolism</subject><subject>Th1 response</subject><issn>0009-9104</issn><issn>1365-2249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV1rFDEYhYModq3-BQmC3s2Yr5kkggVZqhYKgtjrkMlkbJZMsiYz2v57E3dp1Ru9SsJ53sN7cgCAGLUYsf71rsW07xpCmGwJQrRFBEvU3jwAmzvhIdgghGQjy8QJeJLzrjz7viePwQkmglDCyQZcfY7ewjhBb_eLC1BnqAN087yGOMdx9XqJqeqDj3GEcwwxrMZbnaCx3uc3cLbmWgeX51wxbRYXw1PwaNI-22fH8xRcvT__sv3YXH76cLF9d9mYnjDUiEGbsWNcUkk7Mg7M6I6TQXJCMLV2xD3XkvSIC8oYn_AgSk4ukJ24poaO9BScHXz36zDb0diwJO3VPrlZp1sVtVN_KsFdq6_xu8ICCc66YvDqaJDit9XmRc0u12A62LhmxSnDghP5T7BQsmSqji_-AndxTaH8gsKyFxITigskDpBJMedkp7uVMVK1YbVTtUhVi1S1YfWrYXVTRp__Hvl-8FhpAV4eAZ2N9lPSwbh8zzEhO9ahwr09cD-ct7f_vYDanl_UG_0JpEPBFQ</recordid><startdate>200307</startdate><enddate>200307</enddate><creator>SÁNCHEZ‐MARGALET, V.</creator><creator>MARTÍN‐ROMERO, C.</creator><creator>SANTOS‐ALVAREZ, J.</creator><creator>GOBERNA, R.</creator><creator>NAJIB, S.</creator><creator>GONZALEZ‐YANES, C.</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Oxford University Press</general><general>Blackwell Publishing Inc</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>M7N</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200307</creationdate><title>Role of leptin as an immunomodulator of blood mononuclear cells: mechanisms of action</title><author>SÁNCHEZ‐MARGALET, V. ; MARTÍN‐ROMERO, C. ; SANTOS‐ALVAREZ, J. ; GOBERNA, R. ; NAJIB, S. ; GONZALEZ‐YANES, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6240-8bacd547939352db4ca572b972213eed167a9260783447f1b8021780ef7a3c3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adipocytes - metabolism</topic><topic>Apoptosis</topic><topic>Autoimmune Diseases - immunology</topic><topic>Biological and medical sciences</topic><topic>cell activation</topic><topic>Cells, Cultured</topic><topic>cytokine</topic><topic>Cytokines - immunology</topic><topic>Fundamental and applied biological sciences. 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Moreover, leptin has a trophic effect on monocytes, preventing apoptosis induced by serum deprivation. Leptin stimulation activates JAK–STAT, IRS‐1‐PI3K and MAPK signalling pathways. Leptin also stimulates Tyr‐phosphorylation of the RNA‐binding protein Sam68 mediating the dissociation from RNA. In this way, leptin signalling could modulate RNA metabolism. These signal transduction pathways provide possible mechanisms whereby leptin may modulate activation of peripheral blood mononuclear cells. Therefore, these data support the hypothesis regarding leptin as a proinflammatory cytokine with a possible role as a link between the nutritional status and the immune response. Moreover, these immunoregulatory functions of leptin could have some relevance in the pathophysiology of obesity.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>12823272</pmid><doi>10.1046/j.1365-2249.2003.02190.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adipocytes - metabolism
Apoptosis
Autoimmune Diseases - immunology
Biological and medical sciences
cell activation
Cells, Cultured
cytokine
Cytokines - immunology
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Immunobiology
Janus Kinase 1
leptin
Leptin - immunology
Leptin - pharmacology
leptin receptor
Leukocytes, Mononuclear - drug effects
Leukocytes, Mononuclear - immunology
Lymphocyte Activation
lymphocytes
MAP Kinase Signaling System
Medical sciences
Metabolic diseases
Modulation of the immune response (stimulation, suppression)
Nutritional Status
Obesity
Obesity - immunology
PBMC
Phosphatidylinositol 3-Kinases - metabolism
Protein Isoforms - metabolism
Protein-Tyrosine Kinases - metabolism
Receptors, Cell Surface - metabolism
Receptors, Leptin
Reviews
Signal Transduction - physiology
Th1 Cells - metabolism
Th1 response
title Role of leptin as an immunomodulator of blood mononuclear cells: mechanisms of action
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