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From the Department of Pathology, University of Washington, Seattle, Washington
The hypothesis that wound repair is augmented by delivery of
platelet-derived growth factor (PDGF) from platelets and macrophages is
an attractive extrapolation from the known activities of PDGF in cell
culture and in vivo. To test this hypothesis in
mice, we prepared hematopoietic chimeras, in which the
hematopoietic system of a normal adult mouse was replaced by the
hematopoietic system of a PDGF B-chain -/- or +/+ donor. We initiated
local granulation tissue formation either by implanting small surgical
sponges to elicit a foreign body granulation tissue response,
or by ligating the left common carotid to form an organized thrombus.
We found that the absence of hematopoietic PDGF B-chain did not
decrease the extent of granulation tissue or vascular lesion
formation, and that the vascularization of both lesions
increased by
100%. We conclude that PDGF B-chain from cells of
hematopoietic origin, including platelets and
macrophages, is not important for granulation tissue
formation, and that it reduces vascularization of granulation
issue, probably through disabling of the short-range
chemotactic gradients of PDGF that are important for recruiting
pericytes/smooth muscle cells to the endothelium of new
vessels.
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