Regulation of glucose homeostasis by small extracellular vesicles in normal pregnancy and in gestational diabetes
The mechanisms underpinning maternal metabolic adaptations to a healthy pregnancy and in gestational diabetes mellitus (GDM) remain poorly understood. We hypothesized that small extracellular vesicles (sEVs) isolated from healthy pregnant women promote islet glucose‐stimulated insulin secretion (GSI...
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Veröffentlicht in: | The FASEB journal 2020-04, Vol.34 (4), p.5724-5739 |
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creator | James‐Allan, Laura B. Rosario, Frederick J. Barner, Kelsey Lai, Andrew Guanzon, Dominic McIntyre, H. David Lappas, Martha Powell, Theresa L. Salomon, Carlos Jansson, Thomas |
description | The mechanisms underpinning maternal metabolic adaptations to a healthy pregnancy and in gestational diabetes mellitus (GDM) remain poorly understood. We hypothesized that small extracellular vesicles (sEVs) isolated from healthy pregnant women promote islet glucose‐stimulated insulin secretion (GSIS) and peripheral insulin resistance in nonpregnant mice and that sEVs from GDM women fail to stimulate insulin secretion and cause exacerbated insulin resistance. Small EVs were isolated from plasma of nonpregnant, healthy pregnant, and GDM women at 24‐28 weeks of gestation. We developed a novel approach in nonpregnant mice involving a mini‐osmotic pump for continuous 4‐day jugular venous infusion of sEVs and determined their effects on glucose tolerance in vivo and islets and skeletal muscle in vitro. Fasting insulin was elevated in mice infused with pregnant sEVs as compared to sEVs from nonpregnant and GDM women. Mice infused with sEVs from GDM women developed glucose intolerance. GSIS was increased in mice infused with healthy pregnancy sEVs compared to mice receiving nonpregnant sEVs. GSIS and muscle basal insulin signaling, and insulin responsiveness were attenuated in mice infused with GDM sEVs. sEVs represent a novel mechanism regulating maternal glucose homeostasis in pregnancy and we speculate that altered sEV content contributes to the development of GDM. |
doi_str_mv | 10.1096/fj.201902522RR |
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We developed a novel approach in nonpregnant mice involving a mini‐osmotic pump for continuous 4‐day jugular venous infusion of sEVs and determined their effects on glucose tolerance in vivo and islets and skeletal muscle in vitro. Fasting insulin was elevated in mice infused with pregnant sEVs as compared to sEVs from nonpregnant and GDM women. Mice infused with sEVs from GDM women developed glucose intolerance. GSIS was increased in mice infused with healthy pregnancy sEVs compared to mice receiving nonpregnant sEVs. GSIS and muscle basal insulin signaling, and insulin responsiveness were attenuated in mice infused with GDM sEVs. sEVs represent a novel mechanism regulating maternal glucose homeostasis in pregnancy and we speculate that altered sEV content contributes to the development of GDM.</description><identifier>ISSN: 0892-6638</identifier><identifier>EISSN: 1530-6860</identifier><identifier>DOI: 10.1096/fj.201902522RR</identifier><identifier>PMID: 32154621</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Blood Glucose - metabolism ; Diabetes, Gestational - physiopathology ; exosomes ; Extracellular Vesicles - metabolism ; Female ; glucose intolerance ; Glucose Intolerance - physiopathology ; Homeostasis ; Humans ; Insulin Resistance ; Insulin Secretion ; islets of Langerhans ; Mice ; Mice, Inbred C57BL ; Pregnancy ; skeletal muscle</subject><ispartof>The FASEB journal, 2020-04, Vol.34 (4), p.5724-5739</ispartof><rights>2020 Federation of American Societies for Experimental Biology</rights><rights>2020 Federation of American Societies for Experimental Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4719-22fd9ca3b5b2e5a73168be32685d176368317849b32bb1ee6849742d83c047ff3</citedby><cites>FETCH-LOGICAL-c4719-22fd9ca3b5b2e5a73168be32685d176368317849b32bb1ee6849742d83c047ff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1096%2Ffj.201902522RR$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1096%2Ffj.201902522RR$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32154621$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>James‐Allan, Laura B.</creatorcontrib><creatorcontrib>Rosario, Frederick J.</creatorcontrib><creatorcontrib>Barner, Kelsey</creatorcontrib><creatorcontrib>Lai, Andrew</creatorcontrib><creatorcontrib>Guanzon, Dominic</creatorcontrib><creatorcontrib>McIntyre, H. David</creatorcontrib><creatorcontrib>Lappas, Martha</creatorcontrib><creatorcontrib>Powell, Theresa L.</creatorcontrib><creatorcontrib>Salomon, Carlos</creatorcontrib><creatorcontrib>Jansson, Thomas</creatorcontrib><title>Regulation of glucose homeostasis by small extracellular vesicles in normal pregnancy and in gestational diabetes</title><title>The FASEB journal</title><addtitle>FASEB J</addtitle><description>The mechanisms underpinning maternal metabolic adaptations to a healthy pregnancy and in gestational diabetes mellitus (GDM) remain poorly understood. We hypothesized that small extracellular vesicles (sEVs) isolated from healthy pregnant women promote islet glucose‐stimulated insulin secretion (GSIS) and peripheral insulin resistance in nonpregnant mice and that sEVs from GDM women fail to stimulate insulin secretion and cause exacerbated insulin resistance. Small EVs were isolated from plasma of nonpregnant, healthy pregnant, and GDM women at 24‐28 weeks of gestation. We developed a novel approach in nonpregnant mice involving a mini‐osmotic pump for continuous 4‐day jugular venous infusion of sEVs and determined their effects on glucose tolerance in vivo and islets and skeletal muscle in vitro. Fasting insulin was elevated in mice infused with pregnant sEVs as compared to sEVs from nonpregnant and GDM women. Mice infused with sEVs from GDM women developed glucose intolerance. GSIS was increased in mice infused with healthy pregnancy sEVs compared to mice receiving nonpregnant sEVs. GSIS and muscle basal insulin signaling, and insulin responsiveness were attenuated in mice infused with GDM sEVs. sEVs represent a novel mechanism regulating maternal glucose homeostasis in pregnancy and we speculate that altered sEV content contributes to the development of GDM.</description><subject>Animals</subject><subject>Blood Glucose - metabolism</subject><subject>Diabetes, Gestational - physiopathology</subject><subject>exosomes</subject><subject>Extracellular Vesicles - metabolism</subject><subject>Female</subject><subject>glucose intolerance</subject><subject>Glucose Intolerance - physiopathology</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Insulin Resistance</subject><subject>Insulin Secretion</subject><subject>islets of Langerhans</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Pregnancy</subject><subject>skeletal muscle</subject><issn>0892-6638</issn><issn>1530-6860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQhi0EoqWwMiKPLCn-SBxnhIoCUiWkAnNkJ5eQyolbOwH673HVgtiY7nT33KPTi9AlJVNKMnFTraaM0IywhLHl8giNacJJJKQgx2hMZMYiIbgcoTPvV4QQSqg4RSPOaBILRsdos4R6MKpvbIdthWszFNYDfrctWN8r33ist9i3yhgMX71TBRgTDhz-AN8UBjxuOtxZFwi8dlB3qiu2WHXlbl5DcOzcYVk2SkMP_hydVMp4uDjUCXqb37_OHqPF88PT7HYRFXFKs4ixqswKxXWiGSQq5VRIDZwJmZQ0FVxITlMZZ5ozrSmACH0as1LygsRpVfEJut57185uhvBI3jZ-973qwA4-ZzxNZMp5JgI63aOFs947qPK1a1rltjkl-S7mvFrlf2IOB1cH96BbKH_xn1wDkOyBz8bA9h9dPn-5Y4xwmfFvMOCJxg</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>James‐Allan, Laura B.</creator><creator>Rosario, Frederick J.</creator><creator>Barner, Kelsey</creator><creator>Lai, Andrew</creator><creator>Guanzon, Dominic</creator><creator>McIntyre, H. David</creator><creator>Lappas, Martha</creator><creator>Powell, Theresa L.</creator><creator>Salomon, Carlos</creator><creator>Jansson, Thomas</creator><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>202004</creationdate><title>Regulation of glucose homeostasis by small extracellular vesicles in normal pregnancy and in gestational diabetes</title><author>James‐Allan, Laura B. ; Rosario, Frederick J. ; Barner, Kelsey ; Lai, Andrew ; Guanzon, Dominic ; McIntyre, H. David ; Lappas, Martha ; Powell, Theresa L. ; Salomon, Carlos ; Jansson, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4719-22fd9ca3b5b2e5a73168be32685d176368317849b32bb1ee6849742d83c047ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Blood Glucose - metabolism</topic><topic>Diabetes, Gestational - physiopathology</topic><topic>exosomes</topic><topic>Extracellular Vesicles - metabolism</topic><topic>Female</topic><topic>glucose intolerance</topic><topic>Glucose Intolerance - physiopathology</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Insulin Resistance</topic><topic>Insulin Secretion</topic><topic>islets of Langerhans</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Pregnancy</topic><topic>skeletal muscle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>James‐Allan, Laura B.</creatorcontrib><creatorcontrib>Rosario, Frederick J.</creatorcontrib><creatorcontrib>Barner, Kelsey</creatorcontrib><creatorcontrib>Lai, Andrew</creatorcontrib><creatorcontrib>Guanzon, Dominic</creatorcontrib><creatorcontrib>McIntyre, H. David</creatorcontrib><creatorcontrib>Lappas, Martha</creatorcontrib><creatorcontrib>Powell, Theresa L.</creatorcontrib><creatorcontrib>Salomon, Carlos</creatorcontrib><creatorcontrib>Jansson, Thomas</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>The FASEB journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>James‐Allan, Laura B.</au><au>Rosario, Frederick J.</au><au>Barner, Kelsey</au><au>Lai, Andrew</au><au>Guanzon, Dominic</au><au>McIntyre, H. 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We hypothesized that small extracellular vesicles (sEVs) isolated from healthy pregnant women promote islet glucose‐stimulated insulin secretion (GSIS) and peripheral insulin resistance in nonpregnant mice and that sEVs from GDM women fail to stimulate insulin secretion and cause exacerbated insulin resistance. Small EVs were isolated from plasma of nonpregnant, healthy pregnant, and GDM women at 24‐28 weeks of gestation. We developed a novel approach in nonpregnant mice involving a mini‐osmotic pump for continuous 4‐day jugular venous infusion of sEVs and determined their effects on glucose tolerance in vivo and islets and skeletal muscle in vitro. Fasting insulin was elevated in mice infused with pregnant sEVs as compared to sEVs from nonpregnant and GDM women. Mice infused with sEVs from GDM women developed glucose intolerance. GSIS was increased in mice infused with healthy pregnancy sEVs compared to mice receiving nonpregnant sEVs. 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subjects | Animals Blood Glucose - metabolism Diabetes, Gestational - physiopathology exosomes Extracellular Vesicles - metabolism Female glucose intolerance Glucose Intolerance - physiopathology Homeostasis Humans Insulin Resistance Insulin Secretion islets of Langerhans Mice Mice, Inbred C57BL Pregnancy skeletal muscle |
title | Regulation of glucose homeostasis by small extracellular vesicles in normal pregnancy and in gestational diabetes |
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