## Abstract A transient increase in the number of peritoneal colony‐forming cells in agar (PCFC) was noted in the peritoneal cavity of mice given one intraperitoneal injection of thioglycollate medium. This increase of PCFC was not accompanied by a similar degree of increase in the number of either
Peritoneal exudate cells. IV. Characterization of colony forming cells
✍ Scribed by Hsiu-San Lin; Pamela G. Freeman
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 556 KB
- Volume
- 90
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
Abstract
The adherence, phagocytic activity and buoyant density of mouse peritoneal exudate colony forming units (CFU‐PE) were investigated. There was a significant enrichment in the proportion of CFU‐PE in the adherent cells population, defined as cells adhering to a plastic surface within 30 minutes of incubation. The phagocytic activity of CFU‐PE was studied by incubating exudate cells with iron particles for 45 minutes. The cells were then separated into phagocytic and non‐phagocytic cell fractions by passing the incubation mixture through a magnetic field. A significant enrichment of CFU‐PE was seen in the phagocytic cell fraction. When exudate cells were fractionated in a Ficoll discontinuous density gradient, more than 88% of CFU‐PE were recovered at the 16/18% and 18/20% interfaces. It is concluded that CFU‐PE are adherent cells, have strong phagocytic activity and have a buoyant density between 1.0562 and 1.0703. When bone marrow cells were studied by these techniques, the committed stem cells for both granulocytes and macrophages (CFU‐C) were enriched in both non‐adherent cell and non‐phagocytic cells populations. In the Ficoll density gradient, CFU‐C banded at a heavier density region than CFU‐PE.
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## Abstract Mouse peritoneal exudate cells induced by thioglycollate medium can form colonies in soft agar with a plating efficiency of about 5% (0.6%–10%). Cells from an unstimulated peritoneal cavity form no colonies or have a plating efficiency of less than 0.001 %. These colony‐forming cells fr
## Abstract We investigated the effects of age, sex and strain in the induction of peritoneal exudate colony‐forming cells (PE‐CFC) in mice. Sex and age (ranging from 3 weeks to 12 months) had no significant effect on the induction of PE‐CFC. However, we found significant difference between strains
Buoyant density distributions of hemopoietic colony-forming units (CFU) from normal mouse marrow were determined by equilibrium density gradient centrifugation in bovine serum albumin (BSA) gradients. The distributions were compared with those obtained for the total population of nucleated cells fro
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