Partial cDNA sequence of a relaxin-like factor (RLF) receptor, LGR8 and possible existence of the RLF ligand-receptor system in goat testes

Anim Sci J. 2010 Dec;81(6):681-6. doi: 10.1111/j.1740-0929.2010.00801.x. Epub 2010 Oct 29.

Abstract

Relaxin-like factor (RLF), also known as insulin-like factor 3 (INSL3), is produced by testicular Leydig cells, but its specific receptor LGR8 (leucine-rich repeat family of G-protein-coupled receptor 8) has not been identified in goats. This study aimed to identify complementary DNA (cDNA) sequences of goat LGR8, and characterize the expression of both RLF and LGR8 in goat testes by RT-PCR and immunohistochemistry. Testes were collected from immature (3-month-old) and mature (24-month-old) Saanen goats, and partial cDNA sequences of the goat homologue of human LGR8 were identified. The sequence encoded a reduced peptide sequence of 167 amino acids, which corresponded to transmembrane regions 2 through 5, followed by the beginning of intracellular loop 3 of human LGR8. Expression of both LGR8 and RLF genes was drastically increased in mature testes compared with immature ones. Although RLF protein was restricted to Leydig cells, LGR8 protein was detected in both Leydig cells and seminiferous epithelial cells (possibly germ cells and Sertoli cells). These results reveal a possible existence of the RLF-LGR8 ligand-receptor system within the goat testis, suggesting that RLF may play a role in testicular function through LGR8 on Leydig cells and seminiferous epithelial cells in an autocrine and/or paracrine manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autocrine Communication
  • Base Sequence
  • Epithelial Cells / physiology
  • Gene Expression
  • Goats / physiology*
  • Humans
  • Immunohistochemistry
  • Insulin / genetics*
  • Insulin / metabolism*
  • Insulin / physiology
  • Leydig Cells / metabolism
  • Leydig Cells / physiology
  • Male
  • Molecular Sequence Data
  • Paracrine Communication
  • Proteins / genetics*
  • Proteins / metabolism*
  • Proteins / physiology
  • Receptors, G-Protein-Coupled / genetics*
  • Receptors, G-Protein-Coupled / metabolism*
  • Receptors, G-Protein-Coupled / physiology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Seminiferous Epithelium / cytology
  • Sequence Analysis, DNA*
  • Testis / cytology
  • Testis / metabolism*
  • Testis / physiology*

Substances

  • Insulin
  • Leydig insulin-like protein
  • Proteins
  • RXFP2 protein, human
  • Receptors, G-Protein-Coupled