Germline transcripts of the immunoglobulin heavy-chain and T cell receptor genes in a murine hematopoietic stem cell line LyD9 and its derivative cell lines

Immunol Lett. 1991 May;28(2):147-54. doi: 10.1016/0165-2478(91)90113-o.

Abstract

We compared germline transcript levels of immunoglobulin heavy chain and T cell receptor (TcR) genes in a murine hematopoietic stem cell line, LyD9, and its derivative cell lines. LyD9 cells can be induced to differentiate into at least three lineages, namely, B lymphocyte, macrophage, and granulocyte lineages. Although C mu transcripts were found in stem cells to B lymphocytes, other myeloid-committed cells also expressed significant amounts of C mu transcripts. Germline TcR transcripts did not show good correlation with differentiation potential and stages of hematopoietic cells. During this search we identified a novel germline transcript containing the JH-C microliter sequence in LyD9 and some of its derivative cells. Expression of mRNAs for immunoglobulin- and TcR-associated molecules (lambda 5, MB1 and CD3 delta) was widespread except for lambda 5 mRNA. Among three mRNAs encoding putative recombinase proteins, RAG-1 and RAG-2 mRNAs were not expressed in any cell lines tested, while RBP-2 mRNA was expressed ubiquitously.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes
  • Base Sequence
  • Cell Differentiation / drug effects
  • Cell Line
  • DNA Nucleotidyltransferases / genetics
  • Genes, Immunoglobulin*
  • Granulocytes
  • Growth Substances / pharmacology
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / metabolism*
  • Immunoglobulin Heavy Chains / genetics*
  • Integrases*
  • Macrophages
  • Mice
  • Mice, Inbred CBA / genetics
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • RNA, Messenger / genetics*
  • Receptors, Antigen, T-Cell / genetics*
  • Recombinases

Substances

  • Growth Substances
  • Immunoglobulin Heavy Chains
  • RNA, Messenger
  • Receptors, Antigen, T-Cell
  • Recombinases
  • DNA Nucleotidyltransferases
  • Integrases
  • integron integrase IntI1