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Nitric Oxide Increases Arterial Endotheial Permeability through Mediating VE-Cadherin Expression during Arteriogenesis.
Yang, Baolin; Cai, Baizhen; Deng, Panyue; Wu, Xiaoqiong; Guan, Yinglu; Zhang, Bin; Cai, Weijun; Schaper, Jutta; Schaper, Wolfgang.
Afiliación
  • Yang B; Department of Histology & Embryology, School of Basic Medicine, Central South Univ., Changsha, 410078, Hunan, P.R. China; Department of Anatomy, School of Basic Medicine, Nanchang Univ., Nanchang, 330006, Jiangxi, P.R. China.
  • Cai B; Dept. of Intensive Care Unit, the 3rd Xiangya Hospital, Central South Univ., Changsha, 410013, Hunan, P.R. China.
  • Deng P; Department of Histology & Embryology, School of Basic Medicine, Central South Univ., Changsha, 410078, Hunan, P.R. China.
  • Wu X; Department of Anatomy & Neurobiology, School of Basic Medicine, Central South Univ., Changsha, 410013, Hunan, P.R. China.
  • Guan Y; Department of Histology & Embryology, School of Basic Medicine, Central South Univ., Changsha, 410078, Hunan, P.R. China.
  • Zhang B; Department of Histology & Embryology, School of Basic Medicine, Central South Univ., Changsha, 410078, Hunan, P.R. China.
  • Cai W; Department of Histology & Embryology, School of Basic Medicine, Central South Univ., Changsha, 410078, Hunan, P.R. China.
  • Schaper J; Max-Planck-Institute for Heart and Lung Research, Arteriogenesis Research Group, Bad Nauheim, D-61231, Germany.
  • Schaper W; Max-Planck-Institute for Heart and Lung Research, Arteriogenesis Research Group, Bad Nauheim, D-61231, Germany.
PLoS One ; 10(7): e0127931, 2015.
Article en En | MEDLINE | ID: mdl-26133549
Macrophage invasion is an important event during arteriogenesis, but the underlying mechanism is still only partially understood. The present study tested the hypothesis that nitric oxide (NO) and VE-cadherin, two key mediators for vascular permeability, contribute to this event in a rat ischemic hindlimb model. In addition, the effect of NO on expression of VE-caherin and endothelial permeability was also studied in cultured HUVECs. We found that: 1) in normal arteriolar vessels (NAV), eNOS was moderately expressed in endothelial cells (EC) and iNOS was rarely detected. In contrast, in collateral vessels (CVs) induced by simple femoral artery ligation, both eNOS and iNOS were significantly upregulated (P<0.05). Induced iNOS was found mainly in smooth muscle cells, but also in other vascular cells and macrophages; 2) in NAV VE-cadherin was strongly expressed in EC. In CVs, VE-cadherin was significantly downregulated, with a discontinuous and punctate pattern. Administration of nitric oxide donor DETA NONOate (NONOate) further reduced the amounts of Ve-cadherin in CVs, whereas NO synthase inhibitor L-NAME inhibited downregulation of VE-cadherin in CVs; 3) in normal rats Evans blue extravasation (EBE) was low in the musculus gracilis, FITC-dextron leakage was not detected in the vascular wall and few macrophages were observed in perivascular space. In contrast, EBE was significantly increased in femoral artery ligation rats, FITC-dextron leakage and increased amounts of macrophages were detected in CVs, which were further enhanced by administration of NONOate, but inhibited by L-NAME supplement; 4) in vitro experiments confirmed that an increase in NO production reduced VE-cadherin expression, correlated with increases in the permeability of HUVECs. In conclusion, our data for the first time reveal the expression profile of VE-cadherin and alterations of vascular permeability in CVs, suggesting that NO-mediated VE-cadherin pathway may be one important mechanism responsible, at least in part, for macrophage invasion during arteriogenesis.
Asunto(s)
Antígenos CD/genética; Cadherinas/genética; Isquemia/metabolismo; Neovascularización Patológica/metabolismo; Óxido Nítrico Sintasa de Tipo III/genética; Óxido Nítrico Sintasa de Tipo II/genética; Óxido Nítrico/metabolismo; Animales; Antígenos CD/metabolismo; Cadherinas/metabolismo; Permeabilidad Capilar/efectos de los fármacos; Técnicas de Cultivo de Célula; Inhibidores Enzimáticos/farmacología; Arteria Femoral/efectos de los fármacos; Arteria Femoral/metabolismo; Arteria Femoral/patología; Regulación de la Expresión Génica; Miembro Posterior/irrigación sanguínea; Miembro Posterior/metabolismo; Miembro Posterior/patología; Células Endoteliales de la Vena Umbilical Humana/citología; Células Endoteliales de la Vena Umbilical Humana/efectos de los fármacos; Células Endoteliales de la Vena Umbilical Humana/metabolismo; Humanos; Isquemia/genética; Isquemia/patología; Isquemia/prevención & control; Macrófagos/efectos de los fármacos; Macrófagos/metabolismo; Macrófagos/patología; Miocitos del Músculo Liso/citología; Miocitos del Músculo Liso/efectos de los fármacos; Miocitos del Músculo Liso/metabolismo; NG-Nitroarginina Metil Éster/farmacología; Neovascularización Patológica/genética; Neovascularización Patológica/patología; Donantes de Óxido Nítrico/farmacología; Óxido Nítrico Sintasa de Tipo II/metabolismo; Óxido Nítrico Sintasa de Tipo III/metabolismo; Compuestos Nitrosos/farmacología; Ratas; Ratas Sprague-Dawley; Transducción de Señal

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antígenos CD / Cadherinas / Óxido Nítrico Sintasa de Tipo II / Óxido Nítrico Sintasa de Tipo III / Isquemia / Neovascularización Patológica / Óxido Nítrico Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antígenos CD / Cadherinas / Óxido Nítrico Sintasa de Tipo II / Óxido Nítrico Sintasa de Tipo III / Isquemia / Neovascularización Patológica / Óxido Nítrico Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos