The identification of a nonclassical cadherin expressed during B cell development and its interaction with surrogate light chain

J Biol Chem. 2000 Oct 6;275(40):31134-44. doi: 10.1074/jbc.M005901200.

Abstract

A 130-kDa glycoprotein (p130) has been found to be associated with surrogate light chain on pro- and pre-B I cells. Using peptide sequences obtained from purified p130 we have cloned its gene. The gene encodes a typical cadherin type 1 membrane protein with six extracellular cadherin domains (one pseudo domain) but lacking the catenin-binding site in its cytoplasmic part. Even without this catenin-binding site, p130 mediates Ca(2+)-dependent homotypic adhesion of cells. The interaction of p130 with surrogate light chain is confirmed by co-transfection and co-immunoprecipitation experiments. The expression of p130 is biphasic during the B cell development. Reverse transcriptase-polymerase chain reaction and flow cytometric analyses revealed that it is expressed on B220(+)c-Kit(+) pro-B and pre-B-I cells as well as on B220(+)CD25(-)IgM(+) immature and mature B cells but not on B220(+)CD25(+) pre-B-II cells. It is also expressed in fetal liver, at low levels in myeloid cells, and strongly in intestinal epithelial cells. In the spleen, p130-expressing cells are mainly localized in the marginal zone. We call this B lineage-, intestine-, liver- and leukocyte-expressed gene BILL-cadherin. The possible functions of BILL-cadherin in B cell development are discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antibodies, Monoclonal
  • B-Lymphocytes / chemistry
  • B-Lymphocytes / cytology*
  • B-Lymphocytes / metabolism*
  • Base Sequence
  • Binding Sites
  • Blotting, Northern
  • Cadherins / biosynthesis*
  • Cadherins / chemistry
  • Cadherins / genetics*
  • Calcium / metabolism
  • Cell Adhesion
  • Cell Line
  • Cloning, Molecular
  • DNA, Complementary / metabolism
  • Drosophila
  • Female
  • Flow Cytometry
  • Gene Library
  • Immunoglobulin Light Chains / chemistry
  • Immunoglobulin Light Chains, Surrogate
  • Immunoglobulin M / metabolism
  • Immunoglobulin Variable Region / chemistry
  • Intestinal Mucosa / metabolism
  • Leukocyte Common Antigens / metabolism
  • Leukocytes / metabolism
  • Liver / metabolism
  • Membrane Glycoproteins / chemistry*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Precipitin Tests
  • Protein Structure, Tertiary
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1
  • Proto-Oncogene Proteins c-kit / metabolism
  • Rats
  • Receptors, Interleukin-2 / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Tissue Distribution
  • Transfection

Substances

  • Antibodies, Monoclonal
  • Cadherins
  • Cdh17 protein, mouse
  • DNA, Complementary
  • Immunoglobulin Light Chains
  • Immunoglobulin Light Chains, Surrogate
  • Immunoglobulin M
  • Immunoglobulin Variable Region
  • Membrane Glycoproteins
  • Receptors, Interleukin-2
  • Proto-Oncogene Proteins c-kit
  • Leukocyte Common Antigens
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1
  • Calcium

Associated data

  • GENBANK/D87912