Expression of CD1D mRNA transcripts in human choriocarcinoma cell lines and placentally derived trophoblast cells

Immunology. 1999 Apr;96(4):649-55. doi: 10.1046/j.1365-2567.1999.00726.x.

Abstract

Human placental trophoblast is critically involved in mediating maternal tolerance of the fetal semiallograft. Genes encoding highly polymorphic major histocompatibility complex (MHC) class I and class II antigens that could provoke maternal immune rejection responses are silenced in trophoblast. However, several MHC class I or class I-related products exhibiting reduced or negligible polymorphism are expressed and assumed to be functionally involved in maintaining pregnancy. The CD1 gene family encodes non-polymorphic MHC class I-like products that have the unusual ability to present non-peptide antigens to T cells. One member, CD1D, is expressed in certain epithelial cells and interacts with a specific T-cell subset that may promote the development of Th2-mediated responses believed to be associated with pregnancy. In this study we examined the expression of CD1D in human trophoblast cell lines and placentally derived trophoblast cells by reverse transcriptase-polymerase chain reaction using CD1D-specific oligonucleotide primers. We have found that CD1D mRNA transcripts are expressed in trophoblast cells and cell lines. We have also identified a novel alternatively spliced CD1D mRNA transcript lacking exon 4. Exon 4-intact and exon 4-deficient CD1D transcripts appear to be differentially expressed in different trophoblast and non-trophoblast cell populations. Our studies suggest that at least one member of the CD1 family is transcribed in human trophoblast.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD1 / genetics*
  • Antigens, CD1 / metabolism
  • Base Sequence
  • Choriocarcinoma / genetics*
  • Choriocarcinoma / metabolism
  • Female
  • Humans
  • Molecular Sequence Data
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism
  • Pregnancy
  • RNA, Messenger / genetics
  • RNA, Neoplasm / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription, Genetic
  • Trophoblasts / metabolism*
  • Tumor Cells, Cultured
  • Uterine Neoplasms / genetics*
  • Uterine Neoplasms / metabolism

Substances

  • Antigens, CD1
  • Neoplasm Proteins
  • RNA, Messenger
  • RNA, Neoplasm