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J. Cell Biol.,
Volume 141, Number 3, May 4, 1998 805-814
, and Heterotypic Cell-Cell Interactions
Mediate Endothelial Cell-induced Recruitment of 10T1/2
Cells and Their Differentiation to a Smooth Muscle Fate
Harvard Medical School and Children's Hospital, Boston, Massachusetts 02115
We aimed to determine if and how endothelial cells (EC) recruit precursors of smooth muscle cells
and pericytes and induce their differentiation during
vessel formation. Multipotent embryonic 10T1/2 cells
were used as presumptive mural cell precursors. In an
under-agarose coculture, EC induced migration of
10T1/2 cells via platelet-derived growth factor BB.
10T1/2 cells in coculture with EC changed from polygonal to spindle-shaped, reminiscent of smooth muscle
cells in culture. Immunohistochemical and Western blot analyses were used to examine the expression of
smooth muscle (SM)-specific markers in 10T1/2 cells
cultured in the absence and presence of EC. SM-myosin, SM22
, and calponin proteins were undetectable in
10T1/2 cells cultured alone; however, expression of all
three SM-specific proteins was significantly induced in 10T1/2 cells cocultured with EC. Treatment of 10T1/2
cells with TGF-
induced phenotypic changes and
changes in SM markers similar to those seen in the cocultures. Neutralization of TGF-
in the cocultures
blocked expression of the SM markers and the shape change. To assess the ability of 10T1/2 cells to contribute to the developing vessel wall in vivo, prelabeled
10T1/2 cells were grown in a collagen matrix and implanted subcutaneously into mice. The fluorescently
marked cells became incorporated into the medial layer
of developing vessels where they expressed SM markers. These in vitro and in vivo observations shed light
on the cell-cell interactions that occur during vessel development, as well as in pathologies in which developmental processes are recapitulated.
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