In this study, we Investigated whether fibronectin will enhance macrophage uptake of participate complexes of low density llpoprotelns (LDL), heparln, and fibrlllar collagen and whether flbronectln's opsonlc effect could be modulated by the heparln component In these model matrices. We Isolated a heparln fraction (Hep Fn ) based on Its affinity to fibronectin. Hep,= n appeared more charged than unfractionated heparln, as evidenced by enhanced electrophoretlc mobility and ability to effect a cathodlc shift in the electrophoretlc migration of fibronectin.