Bovine milk may be used as a supplement for the serum-free growth of certain fibroblastic cells in culture. The growth properties of three representative cell types in milk-supplemented medium were examined; fibroblastic cell strains, fibroblastic cell lines, and transformed fibroblasts. Transformed fibroblasts, which included RNA and DNA tumor virus-transformed cells and carcinogen-transformed cells, grew in milk. Instead of growing attached to the culture dishes, as they normally do in serum, transformed fibroblasts grew in milk as large clusters in suspension. In contrast, nontransformed fibroblastic cell strains and cell lines did not grow in milk-supplemented medium. Fibroblasts transformed by a temperature-sensitive transformation mutant of Rous sarcoma virus were temperature-sensitive for growth in milk. The failure of cells to adhere to the substratum in milk-supplemented medium suggested that milk might be deficient in attachment factors for fibroblasts. When the attachment of fibroblastic cells in milk-supplemented medium was facilitated by pretreating culture dishes with fibronectin, (a) transformed cells grew attached rather than in suspension, (b) normal cell lines attached and grew to confluence, and (c) normal cell strains adhered and survived but did not exhibit appreciable cell proliferation.
Skip Nav Destination
Article navigation
1 February 1981
Article|
February 01 1981
Serum-free growth of normal and transformed fibroblasts in milk: differential requirements for fibronectin.
K S Steimer
M Klagsbrun
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1981) 88 (2): 294–300.
Citation
K S Steimer, M Klagsbrun; Serum-free growth of normal and transformed fibroblasts in milk: differential requirements for fibronectin.. J Cell Biol 1 February 1981; 88 (2): 294–300. doi: https://doi.org/10.1083/jcb.88.2.294
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement