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MOPC 104E plasmacytoma functional heterogeneity and maturational potential in culture
Abstract:
MOPC 104E plasmacytoma secretes an immunoglobulin M (IgM) paraprotein which reacts specifically with dextran B-1355. We separated plasmacytoma cells into subfractions by density gradient centrifugation. The majority of cells isolated from the peritoneal washes 3 days following i.p. transplantation of tumor were in active cell cycle and had a density of 1.055 or 1.065 g/ml. Cells isolated from 9-day-old ascites were confined to the heavy-density fraction (1.085 g/ml). The majority of these cells were not in proliferative phase. Functional analysis of the fractions using rosette formation and plaque formation assays indicated that cells in active cell cycle had less surface IgM and secreted less IgM than did cells not in cell cycle. An attempt was made to establish a cultured cell line of MOPC 104E plasmacytoma. The majority of the cells of the continuously cultured cell line were in active cell cycle, had less surface IgM, and secreted less IgM. Cultured cells acquired more cell surface IgM and actively secreted IgM following their secondary colonization in 0.8% methylcellulose. These studies showed that the new line of MOPC 104E retained the properties of the original ascites tumor. An important feature of these studies is that the density of cells within a colony is a stable property and is probably not related to cell cycle.
Insights
MOPC 104E plasmacytoma cells in active cell cycle show reduced surface and secreted immunoglobulin M (IgM). Cell density is a stable property, independent of the cell cycle, in this mouse myeloma model.
Area of Science:
- Immunology
- Cell Biology
Background:
- MOPC 104E plasmacytoma is a mouse model that secretes immunoglobulin M (IgM) paraprotein.
- This paraprotein specifically reacts with dextran B-1355.
Purpose of the Study:
- To investigate the relationship between cell cycle, cell density, and IgM production in MOPC 104E plasmacytoma.
- To establish and characterize a cultured cell line of MOPC 104E plasmacytoma.
Main Methods:
- Density gradient centrifugation was used to separate plasmacytoma cells.
- Functional assays including rosette formation and plaque formation were employed.
- A continuous cell culture system was established for MOPC 104E plasmacytoma.
Main Results:
- Cells in active cell cycle (lower density fractions) exhibited less surface and secreted IgM compared to non-proliferative cells (higher density fractions).
- The established cell line maintained properties of the original ascites tumor, with actively cycling cells showing lower IgM levels.
- Secondary colonization in methylcellulose led to increased surface IgM and secretion in cultured cells.
Conclusions:
- Cell cycle status influences IgM expression and secretion in MOPC 104E plasmacytoma.
- Cell density is a stable characteristic, not directly linked to the cell cycle phase in this model.
- The cultured MOPC 104E cell line serves as a valuable tool for studying IgM production and regulation.