Glucocorticoid and thyroid hormones inhibit proliferation of serum-free mouse embryo (SFME) cells
✍ Scribed by Deryk Loo; Cathleen Rawson; Molly Schmitt; Katherine Lindburg; David Barnes
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 785 KB
- Volume
- 142
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Mouse embryo cells derived in a serum‐free medium formulation (SFME cells) do not exhibit growth crisis or chromosomal abnormalities and are nontumorigenic in vivo; these cells are also reversibly growth inhibited by serum or platelet‐free plasma (Loo et al.; Science, 236:200–202, 1987).A portion of the inhibitory activity of serum could be extracted by charcoal, a procedure that removes steroid and thyroid hormones. Both L‐3,5,3′‐triiodothyronine (T3) and hydrocortisone inhibited growth of SFME cells in a reversible manner. The inhibitory activity of serum also was partially removed by treatment with anion exchange resin in a procedure designed to deplete serum of thyroid hormone. However, the effect of serum on untransformed SFME cells could not be prevented by addition of the antiglucocorticoid RU38486, and ras‐transformed clones of SFME cells, which are capable of growing in serum‐containing medium, retained inhibitory responses to glucocorticoid and, with some clonal variability, to T3. These results suggest that glucocorticoid or thyroid hormones may contribute to the inhibitory activity of serum on SFME cells, but additional factors are also involved.
📜 SIMILAR VOLUMES
Serum-free mouse embryo cells, cultured in basal nutrient medium supplemented with insulin, transferrin, epidermal growth factor, fibronectin, and high-density lipoprotein, do not exhibit growth crisis, lack detectable chromosomal aberrations, are nontuniorigenic in vivo, are dependent on epidermal
The relationship between thyroid hormone (triiodothyronine, T(3)) and breast cancer is unclear. We studied the effect of the c-erbA/TR alpha proto-oncogene encoding a functional T(3) receptor (TR alpha 1), of its ligand T(3), and of its retroviral, mutated counterpart, the v-erbA oncogene, on the pr
## Abstract Serum‐free mouse embryo (SFME) cells derived in a defined serum‐free medium have been cultured for more than 200 generations and display properties of neural progenitor cells. SFME cells express the neuroepithelial stem cell marker nestin in defined serumfree medium. Exposure of SFME ce
The procedure of analyzing hormone and growth factor requirements for the growth of MPC-I I cells and of developing a serum-free medium for this cell line has been described. In this medium, MPC-I I cells grow as fast as in serum-supplemented medium, up to 50 generations. MPC-I I cells grown in ser