Absence of detectable IgM in enzymatically or biosynthetically labeled thymus-derived lymphocytes.

Abstract:

:Surface proteins of mouse thymus and spleen cells were radioiodinated with lactoperoxidase. After solubilization, the labeled proteins were precipitated by antibodies directed against mouse immunoglobulin chains; the precipitates were analyzed by radioautography after Na dodecyl sulfate-gel electrophoresis. Radioactive mu and L chains were absent from thymocyte extracts and conspicuous in spleen-cell extracts. The following cells were biosynthetically labeled for 4 hr [(35)S]methionine or 24 hr with [(14)C]leucine: (1) Thymocytes, (2) cortisoneresistant thymocytes [both treated with rabbit antisera cytotoxic to bone marrow-derived (B) lymphocytes and IgM-containing plasma cells, to kill possible contaminating nonthymus-derived cells], (3) "activated thymocytes" (allogeneic cell cultures of cortisone-resistant thymocytes), (4) human Daudi cells (a B lymphoblastic cell line), and (5) purified mouse B spleen lymphocytes devoid of plasma cells. Again no mu and L chains could be detected in thymocyte or thymus-derived cell extracts by immune precipitation and gel electrophoresis, while these chains were conspicuous in B-cell extracts. "Educated thymocytes," obtained from spleens of lethally irradiated mice injected with syngeneic thymocytes and antigen, synthesized mu and L chains under similar conditions; this synthesis resulted from contamination of these cells by IgM-containing plasma cells.

authors

Lisowska-Bernstein B,Rinuy A,Vassalli P

doi

10.1073/pnas.70.10.2879

subject

Has Abstract

pub_date

1973-10-01 00:00:00

pages

2879-83

issue

10

eissn

0027-8424

issn

1091-6490

journal_volume

70

pub_type

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