## Abstract A new spectrofluorometric method for heme quantitation in cultured fibroblasts is described. The method includes: (1) heme extraction by methanol/sulfuric acid, (2) partial purification of heme by a microchromatographic method, and (3) treatment of the purified heme by oxalic acid follo
Proliferation of chick embryo neuroblasts grown in the presence of horse serum requires exogenous transferrin
✍ Scribed by Dr. I. Barakat-Walter; J. C. Deloulme; Dr. M. Sensenbrenner; G. Labourdette
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 859 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Abstract
We have previously shown that neuroblasts from cerebral hemispheres of 6‐day‐old chick embryos are able to proliferate when grown in the presence of fetal calf serum. We report here that in the presence of horse serum alone the proliferative rate of neuroblasts is strongly reduced. A high proliferative rate is restored upon the addition of bovine transferrin and to a lesser extent with added FeSO~4~ or hemin. These findings suggest that the transferrin of horse serum cannot be used by chick neuroblasts in vitro, while bovine transferrin exogenously added is active in promoting cell proliferation. We propose that the stimulatory activity of the fetal calf serum is due to bovine transferrin, since when this serum is fractionated by gel filtration, the fractions that stimulate the proliferation of neuroblasts grown in the presence of horse serum are located in the molecular weight area of transferrin, and they do contain transferrin as seen by immunoblotting with a specific anti‐transferrin antibody.
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