RESUMEN
OBJECTIVE: While shear stress closely regulates vascular remodeling, the mediators of this process have been only partially elucidated. The current study examined the role of the gelatinases in flow-mediated vein graft intimal hyperplasia. We hypothesized that matrix metalloproteinase (MMP)-2 and MMP-9 expression and protein levels, relative to tissue inhibitors of metalloproteinase (TIMP)-1 and TIMP-2, are upregulated in a flow-dependent manner during vein graft arterialization. METHODS: Bilateral common carotid interposition vein grafting was performed in rabbits. Reduction in flow was achieved through unilateral ligation of the internal carotid artery and three of four branches of the external carotid artery. At 28 days grafts were harvested and analyzed for intimal area; MMP-2 and MMP-9, and TIMP-1 and TIMP-2 messenger RNA content, via quantitative reverse transcription polymerase chain reaction; and MMP-2 and MMP-9, and TIMP-1 and TIMP-2 protein concentrations, via both bioactivity assay and zymography. RESULTS: Branch ligation resulted in a 10-fold difference in mean flow rate and accelerated development of intimal hyperplasia in a low-flow environment. Exposure of the vein graft to arterial hemodynamics induced a marked rise in MMP-9 mRNA levels, whereas only a modest increase in MMP-2 mRNA was observed. MMP-2 protein was 50 to 100 times more abundant than MMP-9, and was significantly upregulated in grafts that demonstrated enhanced intimal thickening. Immunohistochemistry demonstrated that MMP-2 was located throughout the myointima, whereas MMP-9 was localized almost exclusively to the region of endothelium. No differences in TIMP-1 and TIMP-2 mRNA or protein levels were detected between high-flow and low-flow grafts. CONCLUSION: MMP-2 is the predominate gelatinase that regulates early vein graft remodeling. Despite a marked increase in MMP-9 gene expression, development of intimal hyperplasia after a reduction in wall shear rate correlates with an increase in MMP-2 protein levels. These data suggest differential regulatory mechanisms for proteases within the remodeling vein graft wall. Modulation of extracellular matrix biologic features may offer therapeutic strategies for the prevention of vein graft failure.
Asunto(s)
Metaloproteinasa 2 de la Matriz/metabolismo , Metaloproteinasa 9 de la Matriz/metabolismo , Túnica Íntima/patología , Animales , Implantación de Prótesis Vascular , Arteria Carótida Común/cirugía , Expresión Génica , Oclusión de Injerto Vascular/patología , Hemorreología , Hiperplasia , Inmunohistoquímica , Venas Yugulares/trasplante , Masculino , Metaloproteinasa 2 de la Matriz/genética , Metaloproteinasa 9 de la Matriz/genética , ARN Mensajero/genética , Conejos , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Inhibidor Tisular de Metaloproteinasa-1/metabolismo , Inhibidor Tisular de Metaloproteinasa-2/metabolismo , Regulación hacia ArribaRESUMEN
Accelerated intimal hyperplasia in response to altered flow environment is critical to the process of vein bypass graft failure. Lack of a reproducible animal model for dissecting the mechanisms of vein graft (VG) remodeling has limited progress toward solving this clinically significant problem. Combining a cuffed anastomotic technique with other surgical manipulations, we developed a well-defined, more robust method for studying hemodynamic factors in VG arterialization. VG with fistula placement, complete occlusion, or partial distal branch ligation (DBL) was performed in the carotid artery of 56 rabbits. Extensive hemodynamic and physiological analyses were performed to define the hemodynamic forces and histological adaptations of the wall at 1-28 days. Anastomotic time averaged 12 min, with 100% patency of bilateral grafts and unilateral grafts plus no adjunct or delayed fistula. Bilateral VG-DBL resulted in an immediate disparity in wall shear (0.8 +/- 0.1 vs. 12.4 +/- 1.1 dyn/cm2, ligated vs. contralateral graft). Grafts exposed to low shear stress responded primarily through enhanced intimal thickening (231 +/- 35 vs. 36 +/- 18 microm, low vs. high shear). High-shear-stress grafts adapted through enhanced outward remodeling, with a 24% increase in lumen diameter at 28 days (3.0 +/- 0.1 vs. 3.7 +/- 0.2 mm, low vs. high shear). We have taken advantage of the cuffed anastomotic technique and combined it with a bilateral VG-DBL model to dissect the impact of hemodynamic forces on VG arterialization. This novel model offers a robust, clinically relevant, statistically powerful small animal model for evaluation of high- and low-shear-regulated VG remodeling.
Asunto(s)
Adaptación Fisiológica , Venas/fisiopatología , Venas/trasplante , Anastomosis Quirúrgica , Animales , Arterias Carótidas/fisiopatología , Arterias Carótidas/cirugía , Adaptabilidad , Hemodinámica , Hiperplasia/patología , Ligadura , Masculino , Conejos , Flujo Sanguíneo Regional , Túnica Íntima/patología , Venas/patologíaRESUMEN
BACKGROUND: Arteriogenesis serves as an efficient mechanism for flow restoration after arterial occlusion. This process is associated with inflammatory mediators such as tumor necrosis factor-alpha (TNF-alpha), although their role in arteriogenesis remains unclear. We hypothesized that arteriogenesis is reduced in mice lacking functional TNF-alpha or p55 receptor. To test this hypothesis, we developed a novel microsphere-based murine model of hindlimb perfusion measurement. METHODS AND RESULTS: Unilateral femoral arteries of nude (n=9), TNF-alpha(-/-) (n=9), TNF-alpha receptor p55(-/-) (n=8), and p75(-/-) (n=8) mice as well as their appropriate genetic background controls were occluded. The nude mice underwent laser Doppler hindlimb flux measurements preoperatively, postoperatively, and after 7 days. Seven days after ligation, all animals underwent tissue perfusion determinations using fluorescent microspheres. Laser Doppler findings confirmed acute decrease in flux with falsely normal values after 1 week. Microsphere results from control mice showed perfusion restoration to values approximately 50% of normal within 7 days. TNF-alpha(-/-) mice demonstrated a significant reduction (45.1%) in collateral artery perfusion compared with controls (TNF-alpha(-/-) 22.4+/-5.1% versus B6x129 49.7+/-9.3%; P<0.01). p55(-/-) mice exhibited an almost identical 45.8% reduction in collateral artery formation (p55(-/-) 28.3+/-4.3% versus C57BL/6J 61.8+/-9.1%; P<0.01), whereas p75(-/-) mice were equivalent to controls (p75(-/-) 54.5+/-5.5%; P=0.13). CONCLUSIONS: Microsphere techniques in mice offer a tool for the molecular dissection of arteriogenesis mechanisms. These results suggest that TNF-alpha positively modulates arteriogenesis probably via signaling through its p55 receptor.
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Antígenos CD/metabolismo , Neovascularización Fisiológica/fisiología , Receptores del Factor de Necrosis Tumoral/metabolismo , Transducción de Señal/fisiología , Factor de Necrosis Tumoral alfa/metabolismo , Animales , Antígenos CD/genética , Velocidad del Flujo Sanguíneo , Arteria Femoral/fisiología , Colorantes Fluorescentes , Miembro Posterior , Flujometría por Láser-Doppler , Ligadura , Ratones , Ratones Endogámicos , Ratones Noqueados , Ratones Desnudos , Microesferas , Modelos Animales , Receptores del Factor de Necrosis Tumoral/deficiencia , Receptores del Factor de Necrosis Tumoral/genética , Receptores Tipo I de Factores de Necrosis Tumoral , Receptores Tipo II del Factor de Necrosis Tumoral , Factor de Necrosis Tumoral alfa/deficiencia , Factor de Necrosis Tumoral alfa/genéticaRESUMEN
The dendritic cell (DC) is the most potent APC of the immune system, capable of stimulating naive T cells to proliferate and differentiate into effector T cells. Recombinant adenovirus (Adv) readily transduces DCs in vitro allowing directed delivery of transgenes that modify DC function and immune responses. In this study we demonstrate that footpad injection of a recombinant Adv readily targets transduction of myeloid and lymphoid DCs in the draining popliteal lymph node, but not in other lymphoid organs. Popliteal DCs transduced with an empty recombinant Adv undergo maturation, as determined by high MHC class II and CD86 expression. However, transduction with vectors expressing human IL-10 limit DC maturation and associated T cell activation in the draining lymph node. The extent of IL-10 expression is dose dependent; transduction with low particle numbers (10(5)) yields only local expression, while transduction with higher particle numbers (10(7) and 10(10)) leads additionally to IL-10 appearance in the circulation. Furthermore, local DC expression of human IL-10 following in vivo transduction with low particle numbers (10(5)) significantly improves survival following cecal ligation and puncture, suggesting that compartmental modulation of DC function profoundly alters the sepsis-induced immune response.
Asunto(s)
Adenovirus Humanos/inmunología , Células Dendríticas/inmunología , Células Dendríticas/metabolismo , Interleucina-10/biosíntesis , Sepsis/inmunología , Sepsis/mortalidad , Adenovirus Humanos/genética , Animales , Caspasa 3 , Inhibidores de Caspasas , Caspasas/metabolismo , Diferenciación Celular/genética , Diferenciación Celular/inmunología , Células Dendríticas/citología , Células Dendríticas/virología , Relación Dosis-Respuesta Inmunológica , Regulación hacia Abajo/genética , Regulación hacia Abajo/inmunología , Femenino , Vectores Genéticos/administración & dosificación , Vectores Genéticos/inmunología , Humanos , Inyecciones Subcutáneas , Interleucina-10/sangre , Interleucina-10/genética , Interleucina-6/antagonistas & inhibidores , Interleucina-6/sangre , Activación de Linfocitos/genética , Ratones , Ratones Endogámicos C57BL , Sepsis/microbiología , Análisis de Supervivencia , Timo/enzimología , Timo/patología , Regulación hacia Arriba/genética , Regulación hacia Arriba/inmunologíaRESUMEN
INTRODUCTION: Overexpression of the anti-inflammatory cytokine interleukin-10 (IL-10) blocks atherosclerotic events in vivo, and IL-10 has been recently hailed as an "immunologic scalpel" for atherosclerosis. Alternatively, mice lacking IL-10 receiving atherogenic diets have increased occlusive lesions. It remains unclear whether such IL-10 modulation broadly applies to other forms of occlusive arterial remodeling. We hypothesized that lack of IL-10 would exacerbate, and exogenous or overexpression of IL-10 would abrogate low shear stress-induced neointimal hyperplasia (NIH). METHODS: Wild-type (WT) and IL-10-deficient (IL-10-/-) mice underwent unilateral common carotid artery (CCA) ligation. Low shear stress in the patent ligated artery results in remodeling and formation of neointima containing BrdU and SMC alpha-actin-positive cells. Additional groups of WT mice underwent CCA ligation and were treated daily with intraperitoneal saline or 1 microg of human IL-10. Chronic delivery gene therapy approaches were also utilized to define the role of IL-10 signaling. WT mice were treated adventitially with 1 x 10(10) adenovirus/green fluorescent protein (Ad/gfp) and an Ad/empty control to confirm the veracity of adventitial delivery. Then, Ad viral IL-10 (vIL-10), Ad/empty, and virus buffer alone were applied directly to the adventitia of the CAA immediately following ligation. In separate experiments, 1 x 10(10) Ad/empty or Ad/vIL-10 was injected intramuscularly. CCAs were perfusion fixed 28 days postligation, the time at which NIH is near maximum. RESULTS: IL-10-/- mice developed identical NIH areas compared to WT controls. Mice receiving IL-10 demonstrated NIH equivalent to saline controls. Mice receiving intramuscular or adventitial Ad/IL-10 developed high serum levels of IL-10 yet formed NIH areas similar to those of controls. Serum IL-10 levels were significantly higher (P = 0.04) with adventitial delivery. Mice treated adventitially with Ad/gfp showed reliable transfection of cells within the adventitia of CAA. No antibody to human IL-10 was found in the sera of intraperitoneal IL-10-treated mice, which failed to attenuate NIH. CONCLUSION: Under the conditions of this experiment, lack of IL-10 does not exacerbate low shear stress-induced NIH, nor does exogenous administration or overexpression of IL-10 attenuate it. Despite high serum levels of vIL-10 in mice treated with ad/vIL-10 adventitially, there appears to be no therapeutic effect despite the confirmed transfection of adventitial cells. Discrepancies between these findings and previous research may be related to IL-10 dosing, inflammation induced by the adenoviral vector, or disparities between the NIH models.