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Pathways followed by membrane recovered from the surface of plasma cells and myeloma cells
Abstract:
Evidence for recovery of surface membrane and its fusion with Golgi cisternae has been obtained previously in several glandular cells. This study was conducted to determine whether or not membrane is similarly retrieved from the surfaces of plasma cells from lymph nodes (of rats immunized with horseradish peroxidase [HRP]) and mouse myeloma cells (RPC 5.4 and X63 Ag 8 cell lines). Electron-dense tracers (cationic and anionic ferritin, HRP) were used to trace the pathways followed by surface membrane recovered by endocytosis, and immunocytochemistry was used to identify the secretory compartments. When plasma cells or myeloma cells were incubated with cationized ferritin (CF), it bound to the cell surfaces and was taken up in endocytic vesicles, for the most part bound to the vesicle membrane. After 30-60 min, it was found increasingly within lysosomes and in several secretory compartments- notably in multiple stacked Golgi cisternae and secretory vacuoles. By immunocytochemistry the secretory product (immunoglobulins) and CF could be demonstrated in the same Golgi components. When myeloma cells were incubated with native (anionic) ferritin or in HRP, these tracers were taken up in much smaller amounts, primarily within the contents of endocytic vesicles. With continued incubation, they appeared only in lysosomes. When cells were doubly incubated, first in CF and then in HRP, both tracers were taken up (often within the same endocytic vesicle), but they maintained their same destinations as when incubated in a single tracer alone: the content marker, HRP, was localized exclusively within the lysosomal system, whereas the membrane marker, CF, was found within elements along the secretory pathway as well as within lysosomes. The findings demonstrate the existence of considerable membrane traffic between the cell membrane and the Golgi cisternae and lysosomes in both normal plasma cells and myeloma cells. Because myeloma cells behave like the glandular cells studied previously with regard to pathways of retrieved surface membrane, they represent a suitable and promising system for further studies of mechanisms and pathways of membrane retrieval and recycling in secretory cells.
Insights
Plasma cells and myeloma cells retrieve surface membrane via endocytosis, recycling it through the Golgi apparatus and lysosomes. This membrane traffic is crucial for secretory cell function.
Area of Science:
- Cell Biology
- Immunology
- Membrane Biology
Background:
- Surface membrane retrieval and fusion with Golgi cisternae is known in glandular cells.
- The fate of surface membrane in plasma cells and myeloma cells remains less understood.
Purpose of the Study:
- To investigate surface membrane retrieval and recycling pathways in plasma cells and mouse myeloma cells.
- To determine if membrane is retrieved similarly to glandular cells.
Main Methods:
- Utilized electron-dense tracers: cationized ferritin (CF), anionic ferritin, and horseradish peroxidase (HRP).
- Employed immunocytochemistry to identify secretory compartments.
- Observed uptake and localization of tracers in plasma and myeloma cells over time.
Main Results:
- Cationized ferritin (membrane marker) was internalized via endocytosis, localized in Golgi cisternae, secretory vacuoles, and lysosomes.
- Horseradish peroxidase (content marker) was internalized in smaller amounts, localized primarily in lysosomes.
- Doubly labeled cells showed CF in secretory pathway and lysosomes, while HRP remained in lysosomes, confirming distinct membrane and content pathways.
Conclusions:
- Demonstrated significant membrane traffic between the cell membrane, Golgi cisternae, and lysosomes in plasma and myeloma cells.
- Myeloma cells serve as a valuable model for studying membrane retrieval and recycling mechanisms in secretory cells, similar to glandular cells.