Expression of leptin receptor in human endometrium and fluctuation during the menstrual cycle

J Clin Endocrinol Metab. 2000 May;85(5):1946-50. doi: 10.1210/jcem.85.5.6567.

Abstract

Leptin is secreted by adipocytes and regulates appetite through interaction with hypothalamic leptin receptors (OB-R). Accumulated evidence shows that leptin is involved in the stimulation of reproductive functions and that local expression of leptin and OB-R in the ovary, oocyte, embryo, and placenta plays a role in early development. To investigate the role of leptin in implantation, we examined the expression of OB-R and leptin in the human endometrium. Northern and Western blot analyses and RT-PCR showed that the long form of OB-R (OB-R(L)) messenger ribonucleic acid (mRNA) and protein were expressed. In contrast, leptin mRNA or protein was not detected. All of the splice variants of OB-R (OB-R(T)) and OB-R(L) transcripts were expressed in 90% and 84% of the cases, respectively. OB-R mRNA expression peaked in the early secretory phase. Decidual tissue of early gestation also expressed OB-R(T) and OB-R(L). Their incidence and abundance were comparable among endometria with benign uterine diseases and disease-free endometria and were not related to a body mass index within the normal range. The present results indicate that OB-R, but not leptin, is expressed in the human endometrium.

MeSH terms

  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics*
  • Endometriosis / genetics
  • Endometriosis / metabolism
  • Endometrium / metabolism*
  • Female
  • Gene Expression Regulation / physiology*
  • Humans
  • Hypothalamus / physiology
  • Leiomyoma / genetics*
  • Leiomyoma / metabolism
  • Menstrual Cycle / metabolism*
  • RNA, Messenger / genetics
  • Receptors, Cell Surface*
  • Receptors, Leptin
  • Reference Values
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription, Genetic*
  • Uterine Diseases / genetics*
  • Uterine Diseases / metabolism
  • Uterine Neoplasms / genetics*
  • Uterine Neoplasms / metabolism

Substances

  • Carrier Proteins
  • LEPR protein, human
  • RNA, Messenger
  • Receptors, Cell Surface
  • Receptors, Leptin