Abstract
Human non-autocrine neuroblastoma cells SK-N-SH and LF require serum for proliferation in vitro. We wished to determine the role of serum-borne insulin-like growth factor I (IGF-I) as mitogen for these cells. Introduction of the monoclonal antibody α-IR3 against human IGF-I receptor reduced proliferation in the presence of fetal bovine serum (FBS). IGF-I (5 n M) was as effective as FBS (10%) in stimulating proliferation. Porcine insulin mimicked the effects of IGF-I, but at a 1000-fold higher concentration. The antibody α-IR3 reduced growth stimulated by IGF-I more effectively than growth stimulated by insulin. Thus, proliferation of human non-autocrine neuroblastoma cells can be effectively manipulated by exogenous IGF-I.
Original language | English (US) |
---|---|
Pages (from-to) | 391-394 |
Number of pages | 4 |
Journal | In Vitro Cellular & Developmental Biology - Animal: Journal of the Society for In Vitro Biology |
Volume | 29 |
Issue number | 5 |
DOIs | |
State | Published - May 1993 |
Keywords
- fetal bovine serum
- insulin
- insulin-like growth factor I
- neuroblastoma
- α-IR antibody
ASJC Scopus subject areas
- Developmental Biology
- Cell Biology