Telomere shortening in intra uterine growth restriction placentas

Tal Biron-Shental*, Rivka Sukenik-Halevy, Yudith Sharon, Ido Laish, Moshe D. Fejgin, Aliza Amiel

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

Introduction: Placentas from pregnancies complicated with IUGR (intrauterine growth restriction) express altered telomere homeostasis. In the current study, we examined mechanisms of telomere shortening in these placentas. Methods: Placental biopsies from 15 IUGR and 15 healthy control pregnancies were examined. The percentage of trophoblasts with fragmented nuclei: senescence-associated heterochromatin foci (SAHF), was calculated using DAPI staining. The amount of human telomerase reverse transcriptase (hTERT) mRNA was evaluated using RtPCR levels of telomere capture using FISH in those samples were estimated. Results: The percentage of trophoblasts with SAHF was higher in IUGR compared to control samples, (25. ±. 13.4% vs. 1.6. ±. 1.6%, P. <. 0.0001), hTERT mRNA was decreased (0.5. ±. 0.2 vs. 0.9. ±. 0.1, P. <. 0.0001) and telomere capture was increased (13.2. ±. 9.7% vs.1.3. ±. 2.5%, P. <. 0.001). Conclusions: We suggest that IUGR placentas express increased signs of senescence as part of the impaired telomere homeostasis. One factor that mediates telomere shortening in these placentas is decreased hTERT mRNA, leading to decreased protein expression and therefore, reduced telomere elongation. Telomere capture, which is a healing process, is increased in IUGR trophoblasts as a compensatory mechanism.

Original languageEnglish
Pages (from-to)465-469
Number of pages5
JournalEarly Human Development
Volume90
Issue number9
DOIs
StatePublished - Sep 2014

Keywords

  • HTERT
  • IUGR
  • Placenta
  • Senescence
  • Telomere
  • Telomere capture
  • Trophoblasts

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