A single-cell level comparison of human inner ear organoids with the human cochlea and vestibular organs
DOI: 10.1016/j.celrep.2023.112623
Authors: Wouter H. van der Valk; Edward S.A. van Beelen; Matthew R. Steinhart; Carl Nist-Lund; Daniel Osorio; John C.M.J. de Groot; Liang Sun; Peter Paul G. van Benthem; Karl R. Koehler; Heiko Locher
Step 1: iPSC/ESC maintainance
day 0 ~ 1
culture “adherent” human PSC in “E8” for “1” days. For ECM, use “vitronectin” at “5.0e-7” “g/m”. Medium should contain factors shown in the following table, and should be changed once in “1” days.
| concentration | unit | |
|---|---|---|
| Normocin | 0.1 | g/l |
| Y-27623 | 1.0e-5 | mol/l |
| EDTA | 5.0e-4 | mol/l |
Ideally, “PSC” should be obtained at the end of culture.
Step 2: Primitive streak 1
day 1 ~ 2 (duration missing in database; assumed 1 day)
culture “spheroid” human PSC in “unspecified medium”. Medium should contain factors shown in the following table.
| concentration | unit | |
|---|---|---|
| BMP4 | 1.2e-6 | g/l |
Step 3: endothelial 1
day 2 ~ 3 (duration missing in database; assumed 1 day)
culture “spheroid” human PSC in “unspecified medium”.
Ideally, “EC” should express “PECAM1” at the end of culture.