Gene expression changes evoked in a venous segment exposed to arterial flow

被引:38
作者
Abeles, Deborah
Kwei, Stephanie
Stavrakis, George
Zhang, Yuzhi
Wang, Eric T.
Garcia-Cardena, Guillermo
机构
[1] Brigham & Womens Hosp, Ctr Excellence Vasc Biol, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Cambridge, MA 02138 USA
关键词
D O I
10.1016/j.jvs.2006.05.043
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: This study was conducted to characterize the coordinated molecular changes evoked in the structure and composition of the wall of a venous segment when exposed to fistula flow. Methods: An arteriovenous shunt was created in adult C57BL/6J mice. Remodeled veins and contralateral control jugular veins were isolated 7 days after surgery. Total RNA was isolated, linearly amplified, and the transcriptional profiles of this early adaptive response were obtained by microarray analysis. Histologic and immunohistochemical analyses were performed on remodeled veins and control veins isolated on days 1, 3, 5, and 7 after surgery to further examine distinct spatial and temporal aspects of this early process. Results: There were 131 significantly upregulated and 165 downregulated genes in the remodeled vein compared with the control jugular vein. Genes involved in extracellular matrix reorganization were highly upregulated. Movat's pentachrome staining revealed ground substance on day 3 that was not observed on day 5. The appearance of elastin fibers was first observed on day 7. Morphometric analysis demonstrated maximum wall thickness on day 3. Immunohistochemical analysis revealed the presence of tenascin-C, thrombospondin, lysyl oxidase, and osteopontin in different cell types at different time points throughout the first week after surgery. Conclusion: Major changes in the organization of the extracellular matrix occur during the early response of venous remodeling. Elastin, tenascin-C, thrombospondin, lysyl oxidase, and osteopontin are expressed within the wall of the remodeling vein resulting in the de novo formation of an extracellular matrix scaffold that may be part of a critical adaptation program being evoked to allow the vessel to cope with its new biomechanical environment.
引用
收藏
页码:863 / 870
页数:8
相关论文
共 39 条
[11]   Murine model of neointimal formation and stenosis in vein grafts [J].
Cooley, BC .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (07) :1180-1185
[12]   Low-pressure environment and remodelling of the forearm vein in Brescia-Cimino haemodialysis access [J].
Corpataux, JM ;
Haesler, E ;
Silacci, P ;
Ris, HB ;
Hayoz, D .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2002, 17 (06) :1057-1062
[13]   PATHOPHYSIOLOGY OF VEIN GRAFT FAILURE - A REVIEW [J].
DAVIES, MG ;
HAGEN, PO .
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 1995, 9 (01) :7-18
[14]   The role of thrombospondin-1 in human disease [J].
Esemuede, N ;
Lee, T ;
Pierre-Paul, D ;
Sumpio, BE ;
Gahtan, V .
JOURNAL OF SURGICAL RESEARCH, 2004, 122 (01) :135-142
[15]   RELEASE OF PLATELET-DERIVED GROWTH-FACTOR ACTIVITY FROM PIG VENOUS ARTERIAL GRAFTS [J].
FRANCIS, SE ;
HUNTER, S ;
HOLT, CM ;
GADSDON, PA ;
ROGERS, S ;
DUFF, GW ;
NEWBY, AC ;
ANGELINI, GD .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1994, 108 (03) :540-548
[16]   Matrix metalloproteinases in vascular remodeling and atherogenesis - The good, the bad, and the ugly [J].
Galis, ZS ;
Khatri, JJ .
CIRCULATION RESEARCH, 2002, 90 (03) :251-262
[17]   OSTEOPONTIN EXPRESSION IN CARDIOVASCULAR-DISEASES [J].
GIACHELLI, CM ;
LIAW, L ;
MURRY, CE ;
SCHWARTZ, SM ;
ALMEIDA, M .
OSTEOPONTIN: ROLE IN CELL SIGNALLING AND ADHESION, 1995, 760 :109-126
[18]  
GIBBONS GH, 1994, NEW ENGL J MED, V330, P1431
[19]   Lysyl oxidase is required for vascular and diaphragmatic development in mice [J].
Hornstra, IK ;
Birge, S ;
Starcher, B ;
Bailey, AJ ;
Mecham, RP ;
Shapiro, SD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (16) :14387-14393
[20]  
[Institute of Laboratory Animal Resources Commission on Life Science National Research Council], 1996, GUID CAR US LAB AN