Plural immunoglobulin synthesis in a single cell: An ultrastructural studyof two cases with three M-proteins

Citation
N. Saito et al., Plural immunoglobulin synthesis in a single cell: An ultrastructural studyof two cases with three M-proteins, ULTRA PATH, 22(6), 1998, pp. 421-429
Citations number
25
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
ULTRASTRUCTURAL PATHOLOGY
ISSN journal
01913123 → ACNP
Volume
22
Issue
6
Year of publication
1998
Pages
421 - 429
Database
ISI
SICI code
0191-3123(199811/12)22:6<421:PISIAS>2.0.ZU;2-H
Abstract
Electrophoresis revealed two cases of malignant lymphoma that each containe d three M-proteins (IgM lambda.IgG kappa.IgG lambda and IgM lambda.IgM kapp a.IgG kappa) in the sera. To determine cellular origin of each M-protein, a typical lymphoid and plasmacytoid cells of both cases were examined by elec tron microscopy. Atypical lymphoid and plasmacytoid cells possessed rough e ndoplasmic reticula (RERs) in varying degrees, as seen by conventional elec tron microscopy, and showed double-stainability for plural antibodies again st immunoglobulins following double stainings of immunoelectron microscopy using immunogold staining. Rabbit antibodies against human IgM, IgG, free k appa-light chain and free A-light chain were used for the immunoelectron mi croscopic staining. By the double staining method, plural immunoglobulins, IgM/IgG, IgM/free kappa, IgM/free lambda, IgG/free kappa, IgG/free lambda a nd free kappa/free lambda, were simultaneously detected in varying degrees in the Golgi area, RERs, and dense bodies of lymphoid and plasmacytoid cell s. In conclusion, this study directly exhibited, through electron microscopy, that plural immunoglobulins were synthesized at the same time in a single c ell, and that the process of immunoglobulin synthesis in the lymphoid and p lasmacytoid cells was different from that in a normal B-cell.