Generation of Leptin Receptor Bone Marrow Chimeras: Recovery From Irradiation, Immune Cellularity, Cytokine Expression, and Metabolic Parameters
Leptin regulates appetite and metabolism but also immunity and inflammation. Although functional leptin receptors (LepR) are expressed on hematopoietic cells, the role of these receptors in regulating immune function in vivo remains controversial. To clarify this issue, we performed bone marrow (BM)...
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Veröffentlicht in: | Obesity (Silver Spring, Md.) Md.), 2010-12, Vol.18 (12), p.2274-2281 |
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description | Leptin regulates appetite and metabolism but also immunity and inflammation. Although functional leptin receptors (LepR) are expressed on hematopoietic cells, the role of these receptors in regulating immune function in vivo remains controversial. To clarify this issue, we performed bone marrow (BM) transplantation between obese db/db mice, lacking LepR, and wild‐type (WT) mice. Results indicate that expression of LepR on BM‐derived cells directly, though partially, regulates spleen and thymus cellularity, although the environment of db mice contributes to maintaining reduced cellularity of these organs. Selective expression of LepR on BM‐derived cells also modulates leptin and adiponectin levels, with induction of a more favorable adipokine environment in the WT→db/db group. However, LepR signaling in BM‐derived cells is not involved in regulation of body weight (BW) and composition, glycemia, hepatosteatosis or adipose tissue inflammation, although it modulates expression of interleukin (IL)‐1β in the brain. Finally, data indicate that db mice have an increased susceptibility to irradiation compared to WT mice in terms of BW loss and recovery of leukocyte counts in peripheral blood. Therefore, interpretation of results obtained using BM chimeras between WT and db mice should take into account the difference in radiation sensitivity between the two types of animals. |
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Although functional leptin receptors (LepR) are expressed on hematopoietic cells, the role of these receptors in regulating immune function in vivo remains controversial. To clarify this issue, we performed bone marrow (BM) transplantation between obese db/db mice, lacking LepR, and wild‐type (WT) mice. Results indicate that expression of LepR on BM‐derived cells directly, though partially, regulates spleen and thymus cellularity, although the environment of db mice contributes to maintaining reduced cellularity of these organs. Selective expression of LepR on BM‐derived cells also modulates leptin and adiponectin levels, with induction of a more favorable adipokine environment in the WT→db/db group. However, LepR signaling in BM‐derived cells is not involved in regulation of body weight (BW) and composition, glycemia, hepatosteatosis or adipose tissue inflammation, although it modulates expression of interleukin (IL)‐1β in the brain. Finally, data indicate that db mice have an increased susceptibility to irradiation compared to WT mice in terms of BW loss and recovery of leukocyte counts in peripheral blood. Therefore, interpretation of results obtained using BM chimeras between WT and db mice should take into account the difference in radiation sensitivity between the two types of animals.</description><identifier>ISSN: 1930-7381</identifier><identifier>EISSN: 1930-739X</identifier><identifier>DOI: 10.1038/oby.2010.84</identifier><identifier>PMID: 20395950</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adiponectin - blood ; Animals ; Body Weight - radiation effects ; Bone Marrow - immunology ; Bone Marrow - metabolism ; Bone Marrow - radiation effects ; Bone Marrow Transplantation ; Brain - metabolism ; Chimerism ; Interleukin-1beta - metabolism ; Leptin - blood ; Leukocyte Count ; Leukocytes - radiation effects ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Obese ; Obesity - metabolism ; Receptors, Leptin - deficiency ; Receptors, Leptin - genetics ; Receptors, Leptin - metabolism ; Signal Transduction - physiology ; Spleen - cytology ; Spleen - immunology ; Thymus Gland - cytology ; Thymus Gland - immunology</subject><ispartof>Obesity (Silver Spring, Md.), 2010-12, Vol.18 (12), p.2274-2281</ispartof><rights>2010 North American Association for the Study of Obesity (NAASO)</rights><rights>Copyright Nature Publishing Group Dec 2010</rights><rights>2010 The Obesity Society 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4736-e468d939e2630c649ed50ba7d7379b403cb2e42b430c185466677bc7a2925f0c3</citedby><cites>FETCH-LOGICAL-c4736-e468d939e2630c649ed50ba7d7379b403cb2e42b430c185466677bc7a2925f0c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1038%2Foby.2010.84$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1038%2Foby.2010.84$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20395950$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gove, Melissa E.</creatorcontrib><creatorcontrib>Sherry, Christina L.</creatorcontrib><creatorcontrib>Pini, Maria</creatorcontrib><creatorcontrib>Fantuzzi, Giamila</creatorcontrib><title>Generation of Leptin Receptor Bone Marrow Chimeras: Recovery From Irradiation, Immune Cellularity, Cytokine Expression, and Metabolic Parameters</title><title>Obesity (Silver Spring, Md.)</title><addtitle>Obesity (Silver Spring)</addtitle><description>Leptin regulates appetite and metabolism but also immunity and inflammation. Although functional leptin receptors (LepR) are expressed on hematopoietic cells, the role of these receptors in regulating immune function in vivo remains controversial. To clarify this issue, we performed bone marrow (BM) transplantation between obese db/db mice, lacking LepR, and wild‐type (WT) mice. Results indicate that expression of LepR on BM‐derived cells directly, though partially, regulates spleen and thymus cellularity, although the environment of db mice contributes to maintaining reduced cellularity of these organs. Selective expression of LepR on BM‐derived cells also modulates leptin and adiponectin levels, with induction of a more favorable adipokine environment in the WT→db/db group. However, LepR signaling in BM‐derived cells is not involved in regulation of body weight (BW) and composition, glycemia, hepatosteatosis or adipose tissue inflammation, although it modulates expression of interleukin (IL)‐1β in the brain. Finally, data indicate that db mice have an increased susceptibility to irradiation compared to WT mice in terms of BW loss and recovery of leukocyte counts in peripheral blood. Therefore, interpretation of results obtained using BM chimeras between WT and db mice should take into account the difference in radiation sensitivity between the two types of animals.</description><subject>Adiponectin - blood</subject><subject>Animals</subject><subject>Body Weight - radiation effects</subject><subject>Bone Marrow - immunology</subject><subject>Bone Marrow - metabolism</subject><subject>Bone Marrow - radiation effects</subject><subject>Bone Marrow Transplantation</subject><subject>Brain - metabolism</subject><subject>Chimerism</subject><subject>Interleukin-1beta - metabolism</subject><subject>Leptin - blood</subject><subject>Leukocyte Count</subject><subject>Leukocytes - radiation effects</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Mice, Obese</subject><subject>Obesity - metabolism</subject><subject>Receptors, Leptin - deficiency</subject><subject>Receptors, Leptin - genetics</subject><subject>Receptors, Leptin - metabolism</subject><subject>Signal Transduction - physiology</subject><subject>Spleen - cytology</subject><subject>Spleen - immunology</subject><subject>Thymus Gland - cytology</subject><subject>Thymus Gland - immunology</subject><issn>1930-7381</issn><issn>1930-739X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kk1v1DAQhiMEoqVw4g6WOPRAt9ix4zgckNpVW1baqgiBBCfLcWapS2Iv46Ql_4KfjNMty8eBk8eeZ17P-HWWPWX0kFGuXoV6PMxp2ilxL9tlFaezklef7m9jxXayRzFeUSokLdjDbCenvCqqgu5mP87AA5reBU_Ciixh3TtP3oNNQUByHDyQc4MYbsj80nUJja-ndLgGHMkpho4sEE3jbiUOyKLrhlQyh7YdWoOuHw_IfOzDV5dOT76vEWK8BY1vyDn0pg6ts-SdQdNBDxgfZw9Wpo3w5G7dyz6ennyYv50tL84W86PlzIqSyxkIqZqKV5BLTq0UFTQFrU3ZlLysakG5rXMQeS1SlqlCSCnLsralyau8WFHL97I3G931UHfQWPA9mlav0XUGRx2M039nvLvUX8K15lLQXMkksH8ngOHbALHXnYs2zW08hCFqxXImqOQikS_-Ia_CgD5Np5OBSYyrgiXq5YayGGJEWG17YXTilE5G68lorSbNZ3-2v2V_OZsAugFuXAvj_7T0xfHn9FOmiZ5vSrzpB4Tfb1GPE5pu_Qm5DL-j</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>Gove, Melissa E.</creator><creator>Sherry, Christina L.</creator><creator>Pini, Maria</creator><creator>Fantuzzi, Giamila</creator><general>Blackwell Publishing Ltd</general><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>K9.</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201012</creationdate><title>Generation of Leptin Receptor Bone Marrow Chimeras: Recovery From Irradiation, Immune Cellularity, Cytokine Expression, and Metabolic Parameters</title><author>Gove, Melissa E. ; 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Although functional leptin receptors (LepR) are expressed on hematopoietic cells, the role of these receptors in regulating immune function in vivo remains controversial. To clarify this issue, we performed bone marrow (BM) transplantation between obese db/db mice, lacking LepR, and wild‐type (WT) mice. Results indicate that expression of LepR on BM‐derived cells directly, though partially, regulates spleen and thymus cellularity, although the environment of db mice contributes to maintaining reduced cellularity of these organs. Selective expression of LepR on BM‐derived cells also modulates leptin and adiponectin levels, with induction of a more favorable adipokine environment in the WT→db/db group. However, LepR signaling in BM‐derived cells is not involved in regulation of body weight (BW) and composition, glycemia, hepatosteatosis or adipose tissue inflammation, although it modulates expression of interleukin (IL)‐1β in the brain. Finally, data indicate that db mice have an increased susceptibility to irradiation compared to WT mice in terms of BW loss and recovery of leukocyte counts in peripheral blood. Therefore, interpretation of results obtained using BM chimeras between WT and db mice should take into account the difference in radiation sensitivity between the two types of animals.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20395950</pmid><doi>10.1038/oby.2010.84</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adiponectin - blood Animals Body Weight - radiation effects Bone Marrow - immunology Bone Marrow - metabolism Bone Marrow - radiation effects Bone Marrow Transplantation Brain - metabolism Chimerism Interleukin-1beta - metabolism Leptin - blood Leukocyte Count Leukocytes - radiation effects Male Mice Mice, Inbred C57BL Mice, Knockout Mice, Obese Obesity - metabolism Receptors, Leptin - deficiency Receptors, Leptin - genetics Receptors, Leptin - metabolism Signal Transduction - physiology Spleen - cytology Spleen - immunology Thymus Gland - cytology Thymus Gland - immunology |
title | Generation of Leptin Receptor Bone Marrow Chimeras: Recovery From Irradiation, Immune Cellularity, Cytokine Expression, and Metabolic Parameters |
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