Have you referred to the paper attached below? Please refer to Table 1.
Article A system for the direct co-culture of endothelium on smooth ...
Proliferative media (PM) that stimulated SMC growth consisted of DMEM supplemented with 10% fetal bovine serum, 10% porcine serum, 0.05 g/L vitamin C, 3 × 10−6 g/L CuSO4, 0.05 m HEPES, 0.05 g/L proline, 0.05 g/L alanine, 0.02 g/L glycine, 10 × 10−9 g/L basic fibroblast growth factor, 10 × 10−9 g/L platelet-derived growth factor, and 1× antibiotic/antimycotic. To induce quiescence of SMCs, the quiescent media (QM) consisted of DMEM/F12 with 0.05 g/L vitamin C, 3 × 10−6 g/L CuSO4, 0.05 m HEPES, 0.05 g/L proline, 0.05 g/L alanine, 0.02 g/L glycine, 1 × insulin, transferrin, and selenium supplement, and 1 × antibiotic/antimycotic.
Prior to co-culture, ECs were grown in PM similar to SMCs except with lower serum content (5% FBS and 5% PS). Since ECs would not grow in the absence of serum, co-culture media consisted of 1 part of PM and 5 part of QM (3.3% serum).
You could use the ratio of EC to SMC cell densities ranging between 1:1 and 1:2 as per the article.