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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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 |
format | Article |
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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><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 & 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&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 & 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. Target tissue resistance</subject><subject>Experiments</subject><subject>Fat cells</subject><subject>Health aspects</subject><subject>Hyperplasia</subject><subject>Immunohistochemistry</subject><subject>Lectins</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Microscopy</subject><subject>Microscopy, Confocal</subject><subject>Models, Animal</subject><subject>Neovascularization, Physiologic</subject><subject>Obesity</subject><subject>Obesity - pathology</subject><subject>Research design</subject><subject>Stromal Cells - physiology</subject><subject>Vascular endothelial growth factor</subject><issn>0012-1797</issn><issn>1939-327X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9km9rFDEQxhdR7Fl94ReQoFgQ3ZpkN9ndl9er1sLBgf_wXcgms9uUXHJNdqn37c16B0flkHmRZPjNM5PhybKXBJ_Toqg-6hbznFRl8yibkaZo8oJWvx5nM4wJTfmmOsmexXiLMeYpnmYnpCrqpijwLBvn2mx8Dw6iicg4tGrTbdiir3A3mgARLayPgK7dAGFj5RZdwHAP4NCl6ToI4AYjB-N69FdIbQeIH9C3Ifi1tGgB1qandBpdWO81-gkxgo3PsyedtBFe7M_T7MfnT98XX_Ll6up6MV_mivGmyTumdcsbrGpMCK14-mZLKC8wJQTrpqzKgrIOM0a1orrkCiveAmDVaUJLTovT7Gynuwn-boQ4iLWJKg0lHfgxigozTmrGEvj6H_DWj8Gl2QQlvKwrwnGC3uygXloQxnV-CFJNimKeIMZqVvFE5UeoacNBWu-gMyn9gD8_wqfQsDbqaMG7BwWJGeD30MsxRlFfLf83zJ5V3lroQaRlL1ZHtVXwMQboxCaYtQxbQbCYvCYmr4nJa4l9td_Z2K5BH8i9uRLwdg_IqKTtgnTKxANX14RwNjV9v-NuTH9zn0wntJEtJCcdLoyL1JYl7T-S3OXb</recordid><startdate>200706</startdate><enddate>200706</enddate><creator>NISHIMURA, Satoshi</creator><creator>MANABE, Ichiro</creator><creator>SUGIURA, Seiryo</creator><creator>NAGASAKI, Mika</creator><creator>HOSOYA, Yumiko</creator><creator>YAMASHITA, Hiroshi</creator><creator>FUJITA, Hideo</creator><creator>OHSUGI, Mitsuru</creator><creator>TOBE, Kazuyuki</creator><creator>KADOWAKI, Takashi</creator><creator>NAGAI, Ryozo</creator><general>American Diabetes Association</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>8GL</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>200706</creationdate><title>Adipogenesis in Obesity Requires Close Interplay Between Differentiating Adipocytes, Stromal Cells, and Blood Vessels</title><author>NISHIMURA, Satoshi ; MANABE, Ichiro ; SUGIURA, Seiryo ; NAGASAKI, Mika ; HOSOYA, Yumiko ; YAMASHITA, Hiroshi ; FUJITA, Hideo ; OHSUGI, Mitsuru ; TOBE, Kazuyuki ; KADOWAKI, Takashi ; NAGAI, Ryozo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5699-f5ddb690c8011276b06b126302110d9474325f0552dc2d46c0c6bee0cfd124623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adipocytes</topic><topic>Adipocytes - cytology</topic><topic>Adipocytes - physiology</topic><topic>Adipose tissue</topic><topic>Adipose Tissue - anatomy & histology</topic><topic>Adipose tissues</topic><topic>Angiogenesis</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood vessels</topic><topic>Blood Vessels - pathology</topic><topic>Body fat</topic><topic>Cell Differentiation</topic><topic>Cells</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Endothelium, Vascular - pathology</topic><topic>Epididymis</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Experiments</topic><topic>Fat cells</topic><topic>Health aspects</topic><topic>Hyperplasia</topic><topic>Immunohistochemistry</topic><topic>Lectins</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Microscopy</topic><topic>Microscopy, Confocal</topic><topic>Models, Animal</topic><topic>Neovascularization, Physiologic</topic><topic>Obesity</topic><topic>Obesity - pathology</topic><topic>Research design</topic><topic>Stromal Cells - physiology</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: High School</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & 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 & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & 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 & 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.
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fulltext | fulltext |
identifier | ISSN: 0012-1797 |
ispartof | Diabetes (New York, N.Y.), 2007-06, Vol.56 (6), p.1517-1526 |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
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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