Population
Vascular smooth muscle cells (VSMCs)
Design
Preclinical
Authors
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Supports selective targeting of calcium influx in PDGF-driven proliferation; leaves open clinical translation from animal models.
PDGF and angiotensin II increase cytosolic free calcium in vascular smooth muscle cells through distinct mechanisms, with PDGF requiring calcium influx for mitogenesis.
Roe et al. (1989) studied this question.