By Wolfgang Schaper, Jutta Schaper
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Our own data show that in growing collateral vessels‚ MMP-2 and MMP-9 are upregulated in the intima and activated‚ compared to the media of the same vessel (Fig. 17). The opposite is true for TIMP-1‚ which is increased‚ however‚ in the intima of mature vessels (Fig. 17‚ 18). This led to the conclusion that vascular remodeling by protein Structural Remodeling during Growth of Collateral Vessels 39 Localization of MMP-2 and TIMP-1 (green‚ nuclei are red) in an actively growing vessel. 17a) The concentration of MMP is high in the neointima and low in the media.
1d) Adhesion of a monocyte to an endothelial cell. and inhibition of smooth muscle cell proliferation4. Confocal microscopy showed that in normal arterioles expression of eNOS is very low‚ but that in growing collateral vessels there is a 6-fold-increase (Fig. 3) that returned to normal levels in mature vessels. These findings and the role of NOS in collateral growth will be discussed more extensively in chapter 5. Recently‚ the possibility has been discussed that endothelial cells may originate from bone marrow-derived progenitor cells circulating in blood (reviewed in 5 ).
Cell. 1996; 87: 1069-78. 54. ICHII T, KOYAMA H, TANAKA S, KIM S, SHIOI A, OKUNO Y, RAINES EW, IWAO H, OTANI S, NISHIZAWA Y. Fibrillar collagen specifically regulates human vascular smooth muscle cell genes involved in cellular responses and the pericellular matrix environment. Circ Res. 2001;88:460-7. 55. BURKE RD, WANG D, JONES VM. Ontogeny of vessell wall components in the outflow tract of the chick. Anat Embryol. 1994;189:447-456. 56. WIBERG C, KLATT AR, WAGENER R, PAULSSON M, BATEMAN JF, HEINEGARD D, MORGELIN M.