Home LiteratureArticle Details
PMID: 118450 Published · ppublish English Journal Article

Evidence for hydrophobic region within heavy chains of mouse B lymphocyte membrane-bound IgM.

Vassalli P, Tedghi R, Lisowska-Bernstein B, Tartakoff A, Jaton JC

Abstract

The gel filtration behavior, in the presence of detergents, of membrane-bound IgM from normal mouse spleen B lymphocytes was compared to that of secretory IgM from mouse plasma cells. The proteins were labeled either by surface radioiodination or biosynthetically with radioactive amino acids. Cell lysates were fractionated on calibrated Sepharose 6B columns in the presence of the detergents Nonidet P-40 or deoxycholate. Eluted fractions were immunoprecipitated and the reduced or unreduced precipitates were analyzed by sodium dodecyl sulfate gel electrophoresis followed by radioautography. Surface (125)I-labeled 8S IgM exhibited a gel filtration pattern in Nonidet P-40 corresponding to much higher apparent molecular weight than that of secretory 8S IgM, a difference that almost disappeared when gel filtration was performed in the presence of deoxycholate, which forms much smaller micelles than does Nonidet P-40. Biosynthetically labeled lymphocytes contain two types of IgM molecules differing in their gel filtration behavior and fate: one identical to secretory 8S IgM of plasma cells and secreted in the medium during chase periods, and the other identical to surface (125)I-labeled IgM and remaining cell-associated. Because the surface-bound 8S IgM was not found to be associated with other labeled molecules, it is likely that the detergent-binding behavior of surface IgM is due to a hydrophobic segment carried by these Ig molecules. That lymphocytes synthesize two types of mu chains was also shown by the use of tunicamycin, an inhibitor of glycosylation. In its presence, two unglycosylated mu chains were observed: one identical in size to that made by tunicamycin-treated plasma cells, and the second slightly larger. Gel filtration in Nonidet P-40 of the cell lysates of tunicamycin-treated lymphocytes showed that the nonsecretory 8S IgM contains this second type of mu chains, whereas the IgM molecules of the secretory type contain plasma cell-like mu chains. It is suggested that membrane IgM mu chains contain a hydrophobic segment which is responsible for its association to the membrane.

MeSH Terms
Animals B-Lymphocytes/immunology Chromatography, Gel Detergents Immunoglobulin Heavy Chains Immunoglobulin M Immunoglobulin mu-Chains Membrane Proteins Mice Molecular Weight Receptors, Antigen, B-Cell Solubility Spleen/immunology Tunicamycin/pharmacology
Chemicals
Detergents Immunoglobulin Heavy Chains Immunoglobulin M Immunoglobulin mu-Chains Membrane Proteins Receptors, Antigen, B-Cell Tunicamycin
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Vassalli P
Tedghi R
Lisowska-Bernstein B
Tartakoff A
Jaton J C
References (15)
15 references, click to expand
  1. B lymphocytes contain three species of mu chains.
    Eur J Immunol. 1978 Dec;8(12):876-80 PMID: 103728
  2. Domains and the hinge region of an immunoglobulin heavy chain are encoded in separate DNA segments.
    Nature. 1979 Feb 22;277(5698):627-33 PMID: 106304
  3. Immunoglobulin heavy chain gene organization in mice: analysis of a myeloma genomic clone containing variable and alpha constant regions.
    Proc Natl Acad Sci U S A. 1979 Feb;76(2):857-61 PMID: 106394
  4. Solubilization of membranes by detergents.
    Biochim Biophys Acta. 1975 Mar 25;415(1):29-79 PMID: 1091302
  5. Evidence against a dimeric structure for membrane-bound HLA antigens.
    Nature. 1975 Nov 20;258(5532):240-2 PMID: 1202349
  6. A procedure for removing red cells and dead cells from lymphoid cell suspensions.
    J Immunol Methods. 1975 Jun;7(2-3):291-300 PMID: 167077
  7. Mouse bone marrow lymphocytes and their differentiation.
    J Immunol. 1974 Sep;113(3):719-28 PMID: 4213258
  8. A film detection method for tritium-labelled proteins and nucleic acids in polyacrylamide gels.
    Eur J Biochem. 1974 Jul 1;46(1):83-8 PMID: 4850204
  9. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
    Nature. 1970 Aug 15;227(5259):680-5 PMID: 5432063
  10. Asparaginyl glycopeptides with a low mannose content are hydrolyzed by endo-beta-N-acetylglucosaminidase H.
    J Biol Chem. 1978 Jul 10;253(13):4508-11 PMID: 659430
  11. Detergent solubilization, purification, and separation of specificities of HLA antigens from a cultured human lymphoblastoid line, RPMI 4265.
    J Biol Chem. 1977 Jul 10;252(13):4682-93 PMID: 68955
  12. The role of polyprenol-linked sugars in glycoprotein synthesis.
    Annu Rev Biochem. 1976;45:95-112 PMID: 786163
  13. Cell surface immunoglobulin. XVI. Polypeptide chain structure of mouse IgM and IgD-like molecule.
    J Immunol. 1976 Feb;116(2):409-15 PMID: 814162
  14. Density differences between membrane and secreted immunoglobins of murine splenocytes.
    Biochemistry. 1977 Jan 11;16(1):145-52 PMID: 831775
  15. Evidence for a C-terminal tyrosine residue in human and mouse B-lymphocyte membrane mu chains.
    Nature. 1978 Apr 6;272(5653):555-7 PMID: 99661
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1979-11-00
Pages
5515-9
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC411679
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com