Abstract

The bcl-2 oncogene is expressed in lymphoid and myeloid cells as well as in neurons and several types of epithelial cells and inhibits programmed cell death (apoptosis). Deregulation by the t(14;18) translocation in lymphoid malignancies induces inappropriate cell survival and serves as one of the steps toward a fully malignant behavior. Using pre- and postembedding immunoelectron microscopy in normal and neoplastic lymphocytes, we demonstrate bcl-2 immunoreactivity to the mitochondrial outer circumference and the nuclear envelope and to a lesser degree to the cell membrane. Mitochondrial staining was patchy, reminiscent of mitochondrial contact zones. Additionally, there was a suggestion of association with nuclear pores. In these regions, transmembrane transport is mediated. This may suggest that bcl-2 exerts its function in this process.

Keywords

Immunoelectron microscopyBiologyCell biologyMyeloidMitochondrionTransmembrane proteinApoptosisOncogeneCellProgrammed cell deathPathologyLymphopoiesisCancer researchHaematopoiesisImmunohistochemistryImmunologyCell cycleReceptorBiochemistryMedicine

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Publication Info

Year
1994
Type
article
Volume
54
Issue
1
Pages
256-60
Citations
191
Access
Closed

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Daphne de Jong, F. Prins, D Y Mason et al. (1994). Subcellular localization of the bcl-2 protein in malignant and normal lymphoid cells.. PubMed , 54 (1) , 256-60.