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Studies on colony formation in vitro by mouse bone marrow cells. II. Action of colony stimulating factor

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TLDR
An analysis was made of some of the processes involved in the stimulation by colony stimulating factor (CSF) of cluster and colony formation by mouse bone marrow cells in agar cultures in vitro, finding that colony formation was shown to be related to the concentration and not the total amount of CSF.
Abstract
An analysis was made of some of the processes involved in the stimulation by colony stimulating factor (CSF) of cluster and colony formation by mouse bone marrow cells in agar cultures in vitro. Colony formation was shown to be related to the concentration and not the total amount of CSF. The concentration of CSF determined the rate of new cluster initiation in cultures and the rate of growth of individual clusters. Colony growth depleted the medium of CSF suggesting that colony cells may utilise CSF during proliferation. Bone marrow cells incubated in agar in the absence of CSF rapidly died or lost their capacity to proliferate and form clusters or colonies. CSF appears (a) to be necessary for survival of cluster-and colony-forming cells or for survival of their proliferative potential, (b) to shorten the lag period before individual cells commence proliferation and (c) to increase the growth rate of individual clusters and colonies.

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Journal ArticleDOI

Design of recombinant stem cell factor-macrophage colony stimulating factor fusion proteins and their biological activity in vitro.

TL;DR: The synergistic effect of SCF and M-CSF moieties in the fusion proteins was demonstrated by the result of clonogenic assay performed with human bone mononuclear, in which both SCF/M-CS fusions induced much higher number of CFU-M than equimolar amount ofSCF or M- CSF or that of two cytokines mixture.
Journal ArticleDOI

Stromal colony-stimulating activity production and myeloid colony- forming cells in human hemopoietic and nonhemopoietic bone marrow

TL;DR: The CSA concentration gradient between PH and DNH bones may contribute to the regulation of granulopoiesis in marrow and to the absence of hemopoiedis distally.
Journal ArticleDOI

Macrophage function in murine allogeneic bone marrow radiation chimeras in the early phase after transplantation.

TL;DR: High frequency of macrophage precursor cells in the spleen and liver and a high natural killer activity in the liver may enable chimeras to survive attacks by opportunistic pathogens.
Journal ArticleDOI

Human lung tissue as a source of colony stimulating activity.

TL;DR: Medium conditioned by human lung tissue was found to contain colony stimulating activity (CSA) and this material was tested against mouse and human bone marrow as target system and gave rise to clonal growth in agar cultures.
References
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Journal ArticleDOI

The growth of mouse bone marrow cells in vitro

TL;DR: A simple in vitro technique for the growth of colonies from single cell suspensions of mouse bone marrow involves the plating of marrow cells in agar on feeder layers of other cells, those from 8-day-old mouse kidney and 17th day mouse embryo being shown to be the most efficient types of feeder layer.
Journal ArticleDOI

Stimulation by normal and leukemic mouse sera of colony formation in vitro by mouse bone marrow cells

TL;DR: Using a modification of the agar gel method for bone marrow culture, serum from various strains of mice has been tested for colony stimulating activity and all colonies were initially mainly granulocytic in nature but later became pure populations of mononuclear cells.
Journal ArticleDOI

Analysis of colonies developing in vitro from mouse bone marrow cells stimulated by kidney feeder layers or leukemic serum

TL;DR: Cell colonies developing in agar cultures from mouse bone marrow cells following stimulation either by neonatal kidney cell feeder layers or AKR lymphoid leukemia serum were mixtures of granulocytic and mononuclear cells.
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