Chorioamniotic membrane senescence: a signal for parturition?
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26025293
DOI
10.1016/j.ajog.2015.05.041
PII: S0002-9378(15)00517-7
Knihovny.cz E-zdroje
- Klíčová slova
- aging, delivery, fetal signals, labor, pregnancy, premature birth, senescence-associated secretory phenotype, sterile inflammation, β-galactosidase,
- MeSH
- amnion cytologie metabolismus ultrastruktura MeSH
- beta-galaktosidasa metabolismus MeSH
- chemokin CCL11 metabolismus MeSH
- chorion cytologie metabolismus ultrastruktura MeSH
- dospělí MeSH
- faktor stimulující granulocyto-makrofágové kolonie metabolismus MeSH
- interleukin-6 metabolismus MeSH
- interleukin-8 metabolismus MeSH
- lidé MeSH
- ligand Fas metabolismus MeSH
- mezibuněčná adhezivní molekula-1 metabolismus MeSH
- mitochondrie ultrastruktura MeSH
- mladý dospělý MeSH
- osteoprotegerin metabolismus MeSH
- plodová voda cytologie metabolismus MeSH
- porod v termínu metabolismus MeSH
- porodní děj metabolismus MeSH
- průřezové studie MeSH
- stárnutí buněk * MeSH
- studie případů a kontrol MeSH
- těhotenství MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladý dospělý MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- beta-galaktosidasa MeSH
- CCL11 protein, human MeSH Prohlížeč
- chemokin CCL11 MeSH
- CXCL8 protein, human MeSH Prohlížeč
- faktor stimulující granulocyto-makrofágové kolonie MeSH
- IL6 protein, human MeSH Prohlížeč
- interleukin-6 MeSH
- interleukin-8 MeSH
- ligand Fas MeSH
- mezibuněčná adhezivní molekula-1 MeSH
- osteoprotegerin MeSH
- TNFRSF11B protein, human MeSH Prohlížeč
OBJECTIVE: Senescence is an important biological phenomenon involved in both physiologic and pathologic processes. We propose that chorioamniotic membrane senescence is a mechanism associated with human parturition. The present study was conducted to explore the association between senescence and normal term parturition by examining the morphologic and biochemical evidences in chorioamniotic membranes. STUDY DESIGN: Chorioamniotic membranes were collected from normal term deliveries; group 1: term labor and group 2: term, not in labor. Senescence-related morphologic changes were determined by transmission electron microscopy and biochemical changes were studied by senescence-associated (SA) β-galactosidase staining. Amniotic fluid samples collected from both term labor and term not in labor were analyzed for 14 SA secretory phenotype (SASP) markers. RESULTS: Morphologic evidence of cellular senescence (enlarged cells and organelles) and a higher number of SA β-galactosidase-stained amnion and chorion cells were observed in chorioamniotic membranes obtained from women in labor at term, when compared to term not in labor. The concentration of proinflammatory SASP markers (granulocyte macrophage colony-stimulating factor, interleukin-6 and -8) was significantly higher in the amniotic fluid of women in labor at term than women not in labor. In contrast, SASP factors that protect against cell death (eotaxin-1, soluble Fas ligand, osteoprotegerin, and intercellular adhesion molecule-1) were significantly lower in the amniotic fluid samples from term labor. CONCLUSION: Morphologic and biochemical features of senescence were more frequent in chorioamniotic membranes from women who experienced term labor. Senescence of chorioamniotic membranes were also associated with amniotic fluid SASP markers.
Department of Obstetrics and Gynecology Charles University Hradec Kralove Czech Republic
Department of Pathology University of Texas Medical Branch Galveston TX
Electron Microscopy Core Laboratory University of Texas Medical Branch Galveston TX
Citace poskytuje Crossref.org