Presence of intact endothelium is the best prevention of narrowing or occlusion of the vascular lumen by thrombosis, or by atherosclerotic intimal thickening, or by spasms. To avoid the occurrence of these common pathogeneic mechanisms of the most prevelent cardiovascular diseases (ischemic disease of heart, brain, periphery), endothelium has to be not only morphologically intact (physically present, without """"""""injury"""""""" in the sence of denudation), it also must function properly. In the past grant periods we have learned to analyze quantitatively the interdependent cell movements which restore the morphologic integrity of the endothelium. We now propose to continue these studies, concentrating on the intercellular communications which coordinate individual cell movements into highly organized, efficient maintenance and repair mechanisms. We have also recognized movement of living cells as an extremely sensitive indicator of vital cell functions in the undisturbed endothelium. Thus we have a new tool to explore quantitatively subtle functional alterations of endothelium, and we can test a new hypothesis which claims that certain cellular movements which we have observed at the border between individual cells may be involved in the control of endothelial permeability to molecules as well as to cells.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL023567-07
Application #
3337280
Study Section
Pathology A Study Section (PTHA)
Project Start
1978-12-01
Project End
1988-09-29
Budget Start
1985-09-30
Budget End
1986-09-29
Support Year
7
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Boston Medical Center
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
Larson, D M; Haudenschild, C C; Beyer, E C (1990) Gap junction messenger RNA expression by vascular wall cells. Circ Res 66:1074-80
Larson, D M; Haudenschild, C C (1988) Junctional transfer in wounded cultures of bovine aortic endothelial cells. Lab Invest 59:373-9
Larson, D M; Carson, M P; Haudenschild, C C (1987) Junctional transfer of small molecules in cultured bovine brain microvascular endothelial cells and pericytes. Microvasc Res 34:184-99
Grunwald, J; Chobanian, A V; Haudenschild, C C (1987) Smooth muscle cell migration and proliferation: atherogenic mechanisms in hypertension. Atherosclerosis 67:215-21
Haudenschild, C C; Grunwald, J (1985) Proliferative heterogeneity of vascular smooth muscle cells and its alteration by injury. Exp Cell Res 157:364-70
Haudenschild, C C; Grunwald, J; Chobanian, A V (1985) Effects of hypertension on migration and proliferation of smooth muscle in culture. Hypertension 7:I101-4
Grunwald, J; Haudenschild, C C (1985) The influence of antiplatelet drugs on injury-stimulated migration of cultured smooth muscle cells. Artery 12:324-36