Leptin Is Produced by Parathyroid Glands and Stimulates Parathyroid Hormone Secretion
OBJECTIVE:We asked if leptin and its cognate receptor were present in normal and diseased parathyroid glands, and if so, whether they had any functional effects on parathyroid hormone (PTH) secretion in parathyroid neoplasms. BACKGROUND:The parathyroid glands acting through PTH play a critical role...
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Veröffentlicht in: | Annals of surgery 2017-12, Vol.266 (6), p.1075-1083 |
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creator | Hoang, Don Broer, Niclas Sosa, Julie A Abitbol, Nathalie Yao, Xiaopan Li, Fangyong Rivera-Molina, Felix Toomre, Derek K Roman, Sanziana A Sue, Gloria Kim, Samuel Li, Alexander Y Callender, Glenda G Simpson, Christine Narayan, Deepak |
description | OBJECTIVE:We asked if leptin and its cognate receptor were present in normal and diseased parathyroid glands, and if so, whether they had any functional effects on parathyroid hormone (PTH) secretion in parathyroid neoplasms.
BACKGROUND:The parathyroid glands acting through PTH play a critical role in the regulation of serum calcium. Based on leptinʼs recently discovered role in bone metabolism, we hypothesized these glands were the sites of a functional interaction between these 2 hormones.
METHODS:From July 2010 to July 2011, 96 patients were enrolled in a prospective study of leptin and hyperparathyroidism, all of whom were enrolled based on their diagnosis of hyperparathyroidism, and their candidacy for surgical intervention provided informed consent. Immediately after parathyroidectomy, 100 to 300 mg of adenomatous or hyperplastic diseased parathyroid tissue was prepared and processed according to requirements of the followingin situ hybridization, immunohistochemistry, immunofluorescence by conventional and spinning disc confocal microscopy, electron microscopy, parathyroid culture, whole organ explant, and animal model assays.
RESULTS:Leptin, leptin receptor (long isoform), and PTH mRNA transcripts and protein were detected in an overlapping fashion in parathyroid chief cells in adenoma and hyperplastic glands, and also in normal parathyroid by in situ hybridization, qRT-PCR, and immunohistochemistry. Confocal microscopy confirmed active exogenous leptin uptake in cultured parathyroid cells. PTH secretion in explants increased in response to leptin and decreased with leptin receptor signaling inhibition by AG490, a JAK2/STAT3 inhibitor. Ob/ob mice injected with mouse leptin exhibited increased PTH levels from baseline.
CONCLUSIONS:Taken together, these data suggest that leptin is a functionally active product of the parathyroid glands and stimulates PTH release. |
doi_str_mv | 10.1097/SLA.0000000000002004 |
format | Article |
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BACKGROUND:The parathyroid glands acting through PTH play a critical role in the regulation of serum calcium. Based on leptinʼs recently discovered role in bone metabolism, we hypothesized these glands were the sites of a functional interaction between these 2 hormones.
METHODS:From July 2010 to July 2011, 96 patients were enrolled in a prospective study of leptin and hyperparathyroidism, all of whom were enrolled based on their diagnosis of hyperparathyroidism, and their candidacy for surgical intervention provided informed consent. Immediately after parathyroidectomy, 100 to 300 mg of adenomatous or hyperplastic diseased parathyroid tissue was prepared and processed according to requirements of the followingin situ hybridization, immunohistochemistry, immunofluorescence by conventional and spinning disc confocal microscopy, electron microscopy, parathyroid culture, whole organ explant, and animal model assays.
RESULTS:Leptin, leptin receptor (long isoform), and PTH mRNA transcripts and protein were detected in an overlapping fashion in parathyroid chief cells in adenoma and hyperplastic glands, and also in normal parathyroid by in situ hybridization, qRT-PCR, and immunohistochemistry. Confocal microscopy confirmed active exogenous leptin uptake in cultured parathyroid cells. PTH secretion in explants increased in response to leptin and decreased with leptin receptor signaling inhibition by AG490, a JAK2/STAT3 inhibitor. Ob/ob mice injected with mouse leptin exhibited increased PTH levels from baseline.
CONCLUSIONS:Taken together, these data suggest that leptin is a functionally active product of the parathyroid glands and stimulates PTH release.</description><identifier>ISSN: 0003-4932</identifier><identifier>EISSN: 1528-1140</identifier><identifier>DOI: 10.1097/SLA.0000000000002004</identifier><identifier>PMID: 27611607</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Adenoma - metabolism ; Animals ; Cells, Cultured ; Humans ; Hyperparathyroidism - metabolism ; Hyperplasia - metabolism ; Immunohistochemistry ; Leptin - metabolism ; Mice, Knockout ; Microscopy, Confocal ; Microscopy, Fluorescence ; Microscopy, Immunoelectron ; Parathyroid Glands - metabolism ; Parathyroid Glands - pathology ; Parathyroid Hormone - secretion ; Parathyroid Neoplasms - metabolism ; Prospective Studies ; Receptors, Leptin - antagonists & inhibitors ; Receptors, Leptin - metabolism ; RNA, Messenger - metabolism</subject><ispartof>Annals of surgery, 2017-12, Vol.266 (6), p.1075-1083</ispartof><rights>Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3564-dc455e803790aaf9d97455517cef1a1b0b3ce62d7dd78f3b89d54f18bcedcd913</citedby><cites>FETCH-LOGICAL-c3564-dc455e803790aaf9d97455517cef1a1b0b3ce62d7dd78f3b89d54f18bcedcd913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27611607$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoang, Don</creatorcontrib><creatorcontrib>Broer, Niclas</creatorcontrib><creatorcontrib>Sosa, Julie A</creatorcontrib><creatorcontrib>Abitbol, Nathalie</creatorcontrib><creatorcontrib>Yao, Xiaopan</creatorcontrib><creatorcontrib>Li, Fangyong</creatorcontrib><creatorcontrib>Rivera-Molina, Felix</creatorcontrib><creatorcontrib>Toomre, Derek K</creatorcontrib><creatorcontrib>Roman, Sanziana A</creatorcontrib><creatorcontrib>Sue, Gloria</creatorcontrib><creatorcontrib>Kim, Samuel</creatorcontrib><creatorcontrib>Li, Alexander Y</creatorcontrib><creatorcontrib>Callender, Glenda G</creatorcontrib><creatorcontrib>Simpson, Christine</creatorcontrib><creatorcontrib>Narayan, Deepak</creatorcontrib><title>Leptin Is Produced by Parathyroid Glands and Stimulates Parathyroid Hormone Secretion</title><title>Annals of surgery</title><addtitle>Ann Surg</addtitle><description>OBJECTIVE:We asked if leptin and its cognate receptor were present in normal and diseased parathyroid glands, and if so, whether they had any functional effects on parathyroid hormone (PTH) secretion in parathyroid neoplasms.
BACKGROUND:The parathyroid glands acting through PTH play a critical role in the regulation of serum calcium. Based on leptinʼs recently discovered role in bone metabolism, we hypothesized these glands were the sites of a functional interaction between these 2 hormones.
METHODS:From July 2010 to July 2011, 96 patients were enrolled in a prospective study of leptin and hyperparathyroidism, all of whom were enrolled based on their diagnosis of hyperparathyroidism, and their candidacy for surgical intervention provided informed consent. Immediately after parathyroidectomy, 100 to 300 mg of adenomatous or hyperplastic diseased parathyroid tissue was prepared and processed according to requirements of the followingin situ hybridization, immunohistochemistry, immunofluorescence by conventional and spinning disc confocal microscopy, electron microscopy, parathyroid culture, whole organ explant, and animal model assays.
RESULTS:Leptin, leptin receptor (long isoform), and PTH mRNA transcripts and protein were detected in an overlapping fashion in parathyroid chief cells in adenoma and hyperplastic glands, and also in normal parathyroid by in situ hybridization, qRT-PCR, and immunohistochemistry. Confocal microscopy confirmed active exogenous leptin uptake in cultured parathyroid cells. PTH secretion in explants increased in response to leptin and decreased with leptin receptor signaling inhibition by AG490, a JAK2/STAT3 inhibitor. Ob/ob mice injected with mouse leptin exhibited increased PTH levels from baseline.
CONCLUSIONS:Taken together, these data suggest that leptin is a functionally active product of the parathyroid glands and stimulates PTH release.</description><subject>Adenoma - metabolism</subject><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Humans</subject><subject>Hyperparathyroidism - metabolism</subject><subject>Hyperplasia - metabolism</subject><subject>Immunohistochemistry</subject><subject>Leptin - metabolism</subject><subject>Mice, Knockout</subject><subject>Microscopy, Confocal</subject><subject>Microscopy, Fluorescence</subject><subject>Microscopy, Immunoelectron</subject><subject>Parathyroid Glands - metabolism</subject><subject>Parathyroid Glands - pathology</subject><subject>Parathyroid Hormone - secretion</subject><subject>Parathyroid Neoplasms - metabolism</subject><subject>Prospective Studies</subject><subject>Receptors, Leptin - antagonists & inhibitors</subject><subject>Receptors, Leptin - metabolism</subject><subject>RNA, Messenger - metabolism</subject><issn>0003-4932</issn><issn>1528-1140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE9LAzEQxYMotla_gUiOXrYm-y_JsRRtCwsWas8hm8zS1d2mJruUfnsjraIenMMMDL_3ZngI3VIypkSwh1UxGZMfFROSnqEhzWIeUZqSczQM2yRKRRIP0JX3r4TQlBN2iQYxyynNCRuidQG7rt7ihcdLZ02vweDygJfKqW5zcLY2eNaorfE4NLzq6rZvVAf-FzG3rrVbwCvQDrrabq_RRaUaDzenOULrp8eX6TwqnmeL6aSIdJLlaWR0mmXAScIEUaoSRrCwyCjTUFFFS1ImGvLYMGMYr5KSC5OlFeVl-FIbQZMRuj_67px978F3sq29hiZ8DLb3kvJMsJgyzgKaHlHtrPcOKrlzdavcQVIiPwOVIVD5N9Aguztd6MsWzLfoK8EA8COwt00Hzr81_R6c3IBqus3_3h8cqYJT</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Hoang, Don</creator><creator>Broer, Niclas</creator><creator>Sosa, Julie A</creator><creator>Abitbol, Nathalie</creator><creator>Yao, Xiaopan</creator><creator>Li, Fangyong</creator><creator>Rivera-Molina, Felix</creator><creator>Toomre, Derek K</creator><creator>Roman, Sanziana A</creator><creator>Sue, Gloria</creator><creator>Kim, Samuel</creator><creator>Li, Alexander Y</creator><creator>Callender, Glenda G</creator><creator>Simpson, Christine</creator><creator>Narayan, Deepak</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</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>7X8</scope></search><sort><creationdate>20171201</creationdate><title>Leptin Is Produced by Parathyroid Glands and Stimulates Parathyroid Hormone Secretion</title><author>Hoang, Don ; Broer, Niclas ; Sosa, Julie A ; Abitbol, Nathalie ; Yao, Xiaopan ; Li, Fangyong ; Rivera-Molina, Felix ; Toomre, Derek K ; Roman, Sanziana A ; Sue, Gloria ; Kim, Samuel ; Li, Alexander Y ; Callender, Glenda G ; Simpson, Christine ; Narayan, Deepak</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3564-dc455e803790aaf9d97455517cef1a1b0b3ce62d7dd78f3b89d54f18bcedcd913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adenoma - metabolism</topic><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Humans</topic><topic>Hyperparathyroidism - metabolism</topic><topic>Hyperplasia - metabolism</topic><topic>Immunohistochemistry</topic><topic>Leptin - metabolism</topic><topic>Mice, Knockout</topic><topic>Microscopy, Confocal</topic><topic>Microscopy, Fluorescence</topic><topic>Microscopy, Immunoelectron</topic><topic>Parathyroid Glands - metabolism</topic><topic>Parathyroid Glands - pathology</topic><topic>Parathyroid Hormone - secretion</topic><topic>Parathyroid Neoplasms - metabolism</topic><topic>Prospective Studies</topic><topic>Receptors, Leptin - antagonists & inhibitors</topic><topic>Receptors, Leptin - metabolism</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoang, Don</creatorcontrib><creatorcontrib>Broer, Niclas</creatorcontrib><creatorcontrib>Sosa, Julie A</creatorcontrib><creatorcontrib>Abitbol, Nathalie</creatorcontrib><creatorcontrib>Yao, Xiaopan</creatorcontrib><creatorcontrib>Li, Fangyong</creatorcontrib><creatorcontrib>Rivera-Molina, Felix</creatorcontrib><creatorcontrib>Toomre, Derek K</creatorcontrib><creatorcontrib>Roman, Sanziana A</creatorcontrib><creatorcontrib>Sue, Gloria</creatorcontrib><creatorcontrib>Kim, Samuel</creatorcontrib><creatorcontrib>Li, Alexander Y</creatorcontrib><creatorcontrib>Callender, Glenda G</creatorcontrib><creatorcontrib>Simpson, Christine</creatorcontrib><creatorcontrib>Narayan, Deepak</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoang, Don</au><au>Broer, Niclas</au><au>Sosa, Julie A</au><au>Abitbol, Nathalie</au><au>Yao, Xiaopan</au><au>Li, Fangyong</au><au>Rivera-Molina, Felix</au><au>Toomre, Derek K</au><au>Roman, Sanziana A</au><au>Sue, Gloria</au><au>Kim, Samuel</au><au>Li, Alexander Y</au><au>Callender, Glenda G</au><au>Simpson, Christine</au><au>Narayan, Deepak</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leptin Is Produced by Parathyroid Glands and Stimulates Parathyroid Hormone Secretion</atitle><jtitle>Annals of surgery</jtitle><addtitle>Ann Surg</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>266</volume><issue>6</issue><spage>1075</spage><epage>1083</epage><pages>1075-1083</pages><issn>0003-4932</issn><eissn>1528-1140</eissn><abstract>OBJECTIVE:We asked if leptin and its cognate receptor were present in normal and diseased parathyroid glands, and if so, whether they had any functional effects on parathyroid hormone (PTH) secretion in parathyroid neoplasms.
BACKGROUND:The parathyroid glands acting through PTH play a critical role in the regulation of serum calcium. Based on leptinʼs recently discovered role in bone metabolism, we hypothesized these glands were the sites of a functional interaction between these 2 hormones.
METHODS:From July 2010 to July 2011, 96 patients were enrolled in a prospective study of leptin and hyperparathyroidism, all of whom were enrolled based on their diagnosis of hyperparathyroidism, and their candidacy for surgical intervention provided informed consent. Immediately after parathyroidectomy, 100 to 300 mg of adenomatous or hyperplastic diseased parathyroid tissue was prepared and processed according to requirements of the followingin situ hybridization, immunohistochemistry, immunofluorescence by conventional and spinning disc confocal microscopy, electron microscopy, parathyroid culture, whole organ explant, and animal model assays.
RESULTS:Leptin, leptin receptor (long isoform), and PTH mRNA transcripts and protein were detected in an overlapping fashion in parathyroid chief cells in adenoma and hyperplastic glands, and also in normal parathyroid by in situ hybridization, qRT-PCR, and immunohistochemistry. Confocal microscopy confirmed active exogenous leptin uptake in cultured parathyroid cells. PTH secretion in explants increased in response to leptin and decreased with leptin receptor signaling inhibition by AG490, a JAK2/STAT3 inhibitor. Ob/ob mice injected with mouse leptin exhibited increased PTH levels from baseline.
CONCLUSIONS:Taken together, these data suggest that leptin is a functionally active product of the parathyroid glands and stimulates PTH release.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>27611607</pmid><doi>10.1097/SLA.0000000000002004</doi><tpages>9</tpages></addata></record> |
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subjects | Adenoma - metabolism Animals Cells, Cultured Humans Hyperparathyroidism - metabolism Hyperplasia - metabolism Immunohistochemistry Leptin - metabolism Mice, Knockout Microscopy, Confocal Microscopy, Fluorescence Microscopy, Immunoelectron Parathyroid Glands - metabolism Parathyroid Glands - pathology Parathyroid Hormone - secretion Parathyroid Neoplasms - metabolism Prospective Studies Receptors, Leptin - antagonists & inhibitors Receptors, Leptin - metabolism RNA, Messenger - metabolism |
title | Leptin Is Produced by Parathyroid Glands and Stimulates Parathyroid Hormone Secretion |
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