A Human Pluripotent Stem Cell-Based Screen for Smooth Muscle Cell Differentiation and Maturation Identifies Inhibitors of Intimal Hyperplasia
DOI: 10.1016/j.stemcr.2019.04.013
Authors: Jue Zhang; Brian E. McIntosh; Bowen Wang; Matthew E. Brown; Mitchell D. Probasco; Sarah Webster; Bret Duffin; Ying Zhou; Lian-Wang Guo; William J. Burlingham; Craig Kent; Michael Ferris; James A. Thomson
Step 1: iPSC/ESC maintainance
day 0 ~ 1 (duration missing in database; assumed 1 day)
culture “adherent” human PSC in “E8”. For ECM, use “Matrigel” at “N/A” “N/A”.
Step 2: Primitive streak 1
day 1 ~ 2 (duration missing in database; assumed 1 day)
culture “adherent” human PSC in “E8”. For ECM, use “Matrigel” at “N/A” “N/A”.
Step 3: Primitive streak 2
day 2 ~ 3 (duration missing in database; assumed 1 day)
culture “adherent” human PSC in “E6 medium”. For ECM, use “Matrigel” at “N/A” “N/A”.
Step 4: mesoderm 1
day 3 ~ 4 (duration missing in database; assumed 1 day)
culture “adherent” human PSC in “unspecified medium”. For ECM, use “Matrigel” at “N/A” “N/A”.
Ideally, “mesoderm” should express “MEOX1” at the end of culture.
Step 5: mesoderm 2
day 4 ~ 9
culture “adherent” human PSC in “unspecified medium” for “5” days. For ECM, use “Matrigel” at “N/A” “N/A”. Medium should contain factors shown in the following table, and should be changed once in “5” days.
| concentration | unit | |
|---|---|---|
| TGF-beta | — | — |
| FGF | — | — |
Ideally, “mesoderm” should be obtained at the end of culture.