Adipogenesis in Obesity Requires Close Interplay Between Differentiating Adipocytes, Stromal Cells, and Blood Vessels

Adipogenesis in Obesity Requires Close Interplay Between Differentiating Adipocytes, Stromal Cells, and Blood Vessels Satoshi Nishimura 1 , Ichiro Manabe 1 2 3 , Mika Nagasaki 1 , Yumiko Hosoya 1 , Hiroshi Yamashita 1 , Hideo Fujita 1 , Mitsuru Ohsugi 4 , Kazuyuki Tobe 4 , Takashi Kadowaki 4 , Ryozo...

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Veröffentlicht in:Diabetes (New York, N.Y.) N.Y.), 2007-06, Vol.56 (6), p.1517-1526
Hauptverfasser: NISHIMURA, Satoshi, MANABE, Ichiro, SUGIURA, Seiryo, NAGASAKI, Mika, HOSOYA, Yumiko, YAMASHITA, Hiroshi, FUJITA, Hideo, OHSUGI, Mitsuru, TOBE, Kazuyuki, KADOWAKI, Takashi, NAGAI, Ryozo
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container_issue 6
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container_title Diabetes (New York, N.Y.)
container_volume 56
creator NISHIMURA, Satoshi
MANABE, Ichiro
SUGIURA, Seiryo
NAGASAKI, Mika
HOSOYA, Yumiko
YAMASHITA, Hiroshi
FUJITA, Hideo
OHSUGI, Mitsuru
TOBE, Kazuyuki
KADOWAKI, Takashi
NAGAI, Ryozo
description Adipogenesis in Obesity Requires Close Interplay Between Differentiating Adipocytes, Stromal Cells, and Blood Vessels Satoshi Nishimura 1 , Ichiro Manabe 1 2 3 , Mika Nagasaki 1 , Yumiko Hosoya 1 , Hiroshi Yamashita 1 , Hideo Fujita 1 , Mitsuru Ohsugi 4 , Kazuyuki Tobe 4 , Takashi Kadowaki 4 , Ryozo Nagai 1 and Seiryo Sugiura 5 1 Department of Cardiovascular Medicine, University of Tokyo, Tokyo, Japan 2 Nano-Bioengineering Education Program, Tokyo, Japan 3 PRESTO, Japan Science and Technology Agency, Kawaguchi City, Japan 4 Department of Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo, Japan 5 Department of Human and Engineered Environmental Studies, Graduate School of Frontier Sciences, University of Tokyo, Tokyo, Japan Address correspondence and reprint requests to Seiryo Sugiura, Department of Human and Engineered Environmental Studies, Graduate School of Frontier Sciences, the University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan. E-mail: sugiura{at}k.u-tokyo.ac.jp Abstract OBJECTIVE—The expansion of adipose tissue mass seen in obesity involves both hyperplasia and hypertrophy of adipocytes. However, little is known about how adipocytes, adipocyte precursors, blood vessels, and stromal cells interact with one another to achieve adipogenesis. RESEARCH DESIGN AND METHODS—We have developed a confocal microscopy-based method of three-dimensional visualization of intact living adipose tissue that enabled us to simultaneously evaluate angiogenesis and adipogenesis in db/db mice. RESULTS—We found that adipocyte differentiation takes place within cell clusters (which we designated adipogenic/angiogenic cell clusters) that contain multiple cell types, including endothelial cells and stromal cells that express CD34 and CD68 and bind lectin. There were close spatial and temporal interrelationships between blood vessel formation and adipogenesis, and the sprouting of new blood vessels from preexisting vasculature was coupled to adipocyte differentiation. CD34 + CD68 + lectin-binding cells could clearly be distinguished from CD34 − CD68 + macrophages, which were scattered in the stroma and did not bind lectin. Adipogenic/angiogenic cell clusters can morphologically and immunohistochemically be distinguished from crown-like structures frequently seen in the late stages of adipose tissue obesity. Administration of anti–vascular endothelial growth factor (VEGF) antibodies inhibited not only angiogenesis but also the formation o
doi_str_mv 10.2337/db06-1749
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E-mail: sugiura{at}k.u-tokyo.ac.jp Abstract OBJECTIVE—The expansion of adipose tissue mass seen in obesity involves both hyperplasia and hypertrophy of adipocytes. However, little is known about how adipocytes, adipocyte precursors, blood vessels, and stromal cells interact with one another to achieve adipogenesis. RESEARCH DESIGN AND METHODS—We have developed a confocal microscopy-based method of three-dimensional visualization of intact living adipose tissue that enabled us to simultaneously evaluate angiogenesis and adipogenesis in db/db mice. RESULTS—We found that adipocyte differentiation takes place within cell clusters (which we designated adipogenic/angiogenic cell clusters) that contain multiple cell types, including endothelial cells and stromal cells that express CD34 and CD68 and bind lectin. There were close spatial and temporal interrelationships between blood vessel formation and adipogenesis, and the sprouting of new blood vessels from preexisting vasculature was coupled to adipocyte differentiation. CD34 + CD68 + lectin-binding cells could clearly be distinguished from CD34 − CD68 + macrophages, which were scattered in the stroma and did not bind lectin. Adipogenic/angiogenic cell clusters can morphologically and immunohistochemically be distinguished from crown-like structures frequently seen in the late stages of adipose tissue obesity. Administration of anti–vascular endothelial growth factor (VEGF) antibodies inhibited not only angiogenesis but also the formation of adipogenic/angiogenic cell clusters, indicating that the coupling of adipogenesis and angiogenesis is essential for differentiation of adipocytes in obesity and that VEGF is a key mediator of that process. CONCLUSIONS—Living tissue imaging techniques provide novel evidence of the dynamic interactions between differentiating adipocytes, stromal cells, and angiogenesis in living obese adipose tissue. BrdU, bromodeoxyuridine HIF, hypoxia inducible factor ROS, reactive oxygen species VGEF, vascular endothelial growth factor Footnotes Published ahead of print at http://diabetes.diabetesjournals.org on 9 April 2007. DOI: 10.2337/db06-1749. Additional information for this article can be found in an online appendix at http://dx.doi.org/10.2337/db06-1749 . The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Accepted March 3, 2007. Received November 3, 2006. DIABETES</description><identifier>ISSN: 0012-1797</identifier><identifier>EISSN: 1939-327X</identifier><identifier>DOI: 10.2337/db06-1749</identifier><identifier>PMID: 17389330</identifier><identifier>CODEN: DIAEAZ</identifier><language>eng</language><publisher>Alexandria, VA: American Diabetes Association</publisher><subject>Adipocytes ; Adipocytes - cytology ; Adipocytes - physiology ; Adipose tissue ; Adipose Tissue - anatomy &amp; histology ; Adipose tissues ; Angiogenesis ; Animals ; Biological and medical sciences ; Blood vessels ; Blood Vessels - pathology ; Body fat ; Cell Differentiation ; Cells ; Diabetes. Impaired glucose tolerance ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Endothelium, Vascular - pathology ; Epididymis ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Experiments ; Fat cells ; Health aspects ; Hyperplasia ; Immunohistochemistry ; Lectins ; Male ; Medical sciences ; Metabolic diseases ; Metabolism ; Mice ; Mice, Inbred Strains ; Microscopy ; Microscopy, Confocal ; Models, Animal ; Neovascularization, Physiologic ; Obesity ; Obesity - pathology ; Research design ; Stromal Cells - physiology ; Vascular endothelial growth factor</subject><ispartof>Diabetes (New York, N.Y.), 2007-06, Vol.56 (6), p.1517-1526</ispartof><rights>2007 INIST-CNRS</rights><rights>COPYRIGHT 2007 American Diabetes Association</rights><rights>Copyright American Diabetes Association Jun 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5699-f5ddb690c8011276b06b126302110d9474325f0552dc2d46c0c6bee0cfd124623</citedby><cites>FETCH-LOGICAL-c5699-f5ddb690c8011276b06b126302110d9474325f0552dc2d46c0c6bee0cfd124623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18811656$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17389330$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NISHIMURA, Satoshi</creatorcontrib><creatorcontrib>MANABE, Ichiro</creatorcontrib><creatorcontrib>SUGIURA, Seiryo</creatorcontrib><creatorcontrib>NAGASAKI, Mika</creatorcontrib><creatorcontrib>HOSOYA, Yumiko</creatorcontrib><creatorcontrib>YAMASHITA, Hiroshi</creatorcontrib><creatorcontrib>FUJITA, Hideo</creatorcontrib><creatorcontrib>OHSUGI, Mitsuru</creatorcontrib><creatorcontrib>TOBE, Kazuyuki</creatorcontrib><creatorcontrib>KADOWAKI, Takashi</creatorcontrib><creatorcontrib>NAGAI, Ryozo</creatorcontrib><title>Adipogenesis in Obesity Requires Close Interplay Between Differentiating Adipocytes, Stromal Cells, and Blood Vessels</title><title>Diabetes (New York, N.Y.)</title><addtitle>Diabetes</addtitle><description>Adipogenesis in Obesity Requires Close Interplay Between Differentiating Adipocytes, Stromal Cells, and Blood Vessels Satoshi Nishimura 1 , Ichiro Manabe 1 2 3 , Mika Nagasaki 1 , Yumiko Hosoya 1 , Hiroshi Yamashita 1 , Hideo Fujita 1 , Mitsuru Ohsugi 4 , Kazuyuki Tobe 4 , Takashi Kadowaki 4 , Ryozo Nagai 1 and Seiryo Sugiura 5 1 Department of Cardiovascular Medicine, University of Tokyo, Tokyo, Japan 2 Nano-Bioengineering Education Program, Tokyo, Japan 3 PRESTO, Japan Science and Technology Agency, Kawaguchi City, Japan 4 Department of Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo, Japan 5 Department of Human and Engineered Environmental Studies, Graduate School of Frontier Sciences, University of Tokyo, Tokyo, Japan Address correspondence and reprint requests to Seiryo Sugiura, Department of Human and Engineered Environmental Studies, Graduate School of Frontier Sciences, the University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan. E-mail: sugiura{at}k.u-tokyo.ac.jp Abstract OBJECTIVE—The expansion of adipose tissue mass seen in obesity involves both hyperplasia and hypertrophy of adipocytes. However, little is known about how adipocytes, adipocyte precursors, blood vessels, and stromal cells interact with one another to achieve adipogenesis. RESEARCH DESIGN AND METHODS—We have developed a confocal microscopy-based method of three-dimensional visualization of intact living adipose tissue that enabled us to simultaneously evaluate angiogenesis and adipogenesis in db/db mice. RESULTS—We found that adipocyte differentiation takes place within cell clusters (which we designated adipogenic/angiogenic cell clusters) that contain multiple cell types, including endothelial cells and stromal cells that express CD34 and CD68 and bind lectin. There were close spatial and temporal interrelationships between blood vessel formation and adipogenesis, and the sprouting of new blood vessels from preexisting vasculature was coupled to adipocyte differentiation. CD34 + CD68 + lectin-binding cells could clearly be distinguished from CD34 − CD68 + macrophages, which were scattered in the stroma and did not bind lectin. Adipogenic/angiogenic cell clusters can morphologically and immunohistochemically be distinguished from crown-like structures frequently seen in the late stages of adipose tissue obesity. Administration of anti–vascular endothelial growth factor (VEGF) antibodies inhibited not only angiogenesis but also the formation of adipogenic/angiogenic cell clusters, indicating that the coupling of adipogenesis and angiogenesis is essential for differentiation of adipocytes in obesity and that VEGF is a key mediator of that process. CONCLUSIONS—Living tissue imaging techniques provide novel evidence of the dynamic interactions between differentiating adipocytes, stromal cells, and angiogenesis in living obese adipose tissue. BrdU, bromodeoxyuridine HIF, hypoxia inducible factor ROS, reactive oxygen species VGEF, vascular endothelial growth factor Footnotes Published ahead of print at http://diabetes.diabetesjournals.org on 9 April 2007. DOI: 10.2337/db06-1749. Additional information for this article can be found in an online appendix at http://dx.doi.org/10.2337/db06-1749 . The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Accepted March 3, 2007. Received November 3, 2006. DIABETES</description><subject>Adipocytes</subject><subject>Adipocytes - cytology</subject><subject>Adipocytes - physiology</subject><subject>Adipose tissue</subject><subject>Adipose Tissue - anatomy &amp; histology</subject><subject>Adipose tissues</subject><subject>Angiogenesis</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood vessels</subject><subject>Blood Vessels - pathology</subject><subject>Body fat</subject><subject>Cell Differentiation</subject><subject>Cells</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Endothelium, Vascular - pathology</subject><subject>Epididymis</subject><subject>Etiopathogenesis. Screening. Investigations. 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Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetes (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NISHIMURA, Satoshi</au><au>MANABE, Ichiro</au><au>SUGIURA, Seiryo</au><au>NAGASAKI, Mika</au><au>HOSOYA, Yumiko</au><au>YAMASHITA, Hiroshi</au><au>FUJITA, Hideo</au><au>OHSUGI, Mitsuru</au><au>TOBE, Kazuyuki</au><au>KADOWAKI, Takashi</au><au>NAGAI, Ryozo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adipogenesis in Obesity Requires Close Interplay Between Differentiating Adipocytes, Stromal Cells, and Blood Vessels</atitle><jtitle>Diabetes (New York, N.Y.)</jtitle><addtitle>Diabetes</addtitle><date>2007-06</date><risdate>2007</risdate><volume>56</volume><issue>6</issue><spage>1517</spage><epage>1526</epage><pages>1517-1526</pages><issn>0012-1797</issn><eissn>1939-327X</eissn><coden>DIAEAZ</coden><abstract>Adipogenesis in Obesity Requires Close Interplay Between Differentiating Adipocytes, Stromal Cells, and Blood Vessels Satoshi Nishimura 1 , Ichiro Manabe 1 2 3 , Mika Nagasaki 1 , Yumiko Hosoya 1 , Hiroshi Yamashita 1 , Hideo Fujita 1 , Mitsuru Ohsugi 4 , Kazuyuki Tobe 4 , Takashi Kadowaki 4 , Ryozo Nagai 1 and Seiryo Sugiura 5 1 Department of Cardiovascular Medicine, University of Tokyo, Tokyo, Japan 2 Nano-Bioengineering Education Program, Tokyo, Japan 3 PRESTO, Japan Science and Technology Agency, Kawaguchi City, Japan 4 Department of Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo, Japan 5 Department of Human and Engineered Environmental Studies, Graduate School of Frontier Sciences, University of Tokyo, Tokyo, Japan Address correspondence and reprint requests to Seiryo Sugiura, Department of Human and Engineered Environmental Studies, Graduate School of Frontier Sciences, the University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan. E-mail: sugiura{at}k.u-tokyo.ac.jp Abstract OBJECTIVE—The expansion of adipose tissue mass seen in obesity involves both hyperplasia and hypertrophy of adipocytes. However, little is known about how adipocytes, adipocyte precursors, blood vessels, and stromal cells interact with one another to achieve adipogenesis. RESEARCH DESIGN AND METHODS—We have developed a confocal microscopy-based method of three-dimensional visualization of intact living adipose tissue that enabled us to simultaneously evaluate angiogenesis and adipogenesis in db/db mice. RESULTS—We found that adipocyte differentiation takes place within cell clusters (which we designated adipogenic/angiogenic cell clusters) that contain multiple cell types, including endothelial cells and stromal cells that express CD34 and CD68 and bind lectin. There were close spatial and temporal interrelationships between blood vessel formation and adipogenesis, and the sprouting of new blood vessels from preexisting vasculature was coupled to adipocyte differentiation. CD34 + CD68 + lectin-binding cells could clearly be distinguished from CD34 − CD68 + macrophages, which were scattered in the stroma and did not bind lectin. Adipogenic/angiogenic cell clusters can morphologically and immunohistochemically be distinguished from crown-like structures frequently seen in the late stages of adipose tissue obesity. Administration of anti–vascular endothelial growth factor (VEGF) antibodies inhibited not only angiogenesis but also the formation of adipogenic/angiogenic cell clusters, indicating that the coupling of adipogenesis and angiogenesis is essential for differentiation of adipocytes in obesity and that VEGF is a key mediator of that process. CONCLUSIONS—Living tissue imaging techniques provide novel evidence of the dynamic interactions between differentiating adipocytes, stromal cells, and angiogenesis in living obese adipose tissue. BrdU, bromodeoxyuridine HIF, hypoxia inducible factor ROS, reactive oxygen species VGEF, vascular endothelial growth factor Footnotes Published ahead of print at http://diabetes.diabetesjournals.org on 9 April 2007. DOI: 10.2337/db06-1749. Additional information for this article can be found in an online appendix at http://dx.doi.org/10.2337/db06-1749 . The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Accepted March 3, 2007. Received November 3, 2006. DIABETES</abstract><cop>Alexandria, VA</cop><pub>American Diabetes Association</pub><pmid>17389330</pmid><doi>10.2337/db06-1749</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Adipocytes
Adipocytes - cytology
Adipocytes - physiology
Adipose tissue
Adipose Tissue - anatomy & histology
Adipose tissues
Angiogenesis
Animals
Biological and medical sciences
Blood vessels
Blood Vessels - pathology
Body fat
Cell Differentiation
Cells
Diabetes. Impaired glucose tolerance
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Endothelium, Vascular - pathology
Epididymis
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Experiments
Fat cells
Health aspects
Hyperplasia
Immunohistochemistry
Lectins
Male
Medical sciences
Metabolic diseases
Metabolism
Mice
Mice, Inbred Strains
Microscopy
Microscopy, Confocal
Models, Animal
Neovascularization, Physiologic
Obesity
Obesity - pathology
Research design
Stromal Cells - physiology
Vascular endothelial growth factor
title Adipogenesis in Obesity Requires Close Interplay Between Differentiating Adipocytes, Stromal Cells, and Blood Vessels
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