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Data Supplement for Arteriosclerosis, Thrombosis, and Vascular Biology: Volume 20, Issue 4 -- Page 1013
This item has the following additional materials available:
Data Files
- Figure I. A, Effect of pertussis toxin on LPA0-induced FBHE cell migration. FBHE cells were pretreated overnight with pertussis toxin at the indicated concentrations. Two concentrations on LPA were used to stimulate FBHE cell migration. B, Effect of Mek-1 inhibitor, PD98059, on LPA-induced FBHE cell migration. FBHE cells were pretreated at the indicated concentrations. Three concentrations of LPA were used to stimulate FBHE cell migration. Experimental conditions were as described in print Figure 1. Data are expressed as mean±SD (n=9) and are from a representative experiment that was repeated two times.
- Figure II. Effect of C3 toxin on LPA-induced FBHE cell mingration. Experimental conditions were as described in print Figure 1. FBHE cells were pretreated overnight with C3 toxin at the indicated concentrations. Three concentrations of LPA were used to stimulate FBHA cell migration. Data are expressed as mean±SD (n=9) and are from a representative experiment that was repeated three times.
- Figure III. Effects of PI3-kinase inhibitors, LY294002 and wortmannin, on LPA- and serum-induced FBHE cell migration. Experimental conditions were as described in print Figure 2. FBHE cells were pretreated for 30 to 60 min with LY294002 (A) or wortmannin (B) at the indicated concentrations. LPA (1 µmol/L) or 10% FBS were used to stimulate FBHE cell migration. Data are expressed as mean±SD (n=9) and are from a representative experiment repeated three times.
Prepared by: the Data Supplement Manager
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