Abstract
The objective of this study was to compare two of the inflammatory cytokines (IL-1 and IL-6) elevated in both preterm labour and preterm premature rupture of the membranes (pPROM), with respect to their ability to induce fetal membrane apoptosis. Fetal membranes collected from women at term were placed in an organ explant system and stimulated with recombinant human IL-1β and IL-6. The expression patterns of pro-apoptotic genes (Fas, FasL, TRADD, FADD) and caspases 2, 3, 8, 9 were studied using PCR. Caspase activity and DNA fragmentation were studied using substrate assays and TUNEL respectively. Caspase 8 and 9 expressions were induced in IL-1β and IL-6 treated amniochorion. Caspase 2 expression was seen only in IL-1β stimulated tissues. When compared to control, IL-1β increased caspase 2, 3, 8 and 9 activities, whereas IL-6 treated membranes did not exhibit a significant change. DNA fragmentation was seen in greater numbers after IL-1β treatment than after IL-6 treatment. This study demonstrates that IL-1β is a better inducer of apoptosis in normal human fetal membranes than IL-6.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 922-928 |
| Number of pages | 7 |
| Journal | Placenta |
| Volume | 24 |
| Issue number | 10 |
| DOIs | |
| State | Published - Nov 2003 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Obstetrics and Gynecology
Cite this
IL-1β is a better inducer of apoptosis in human fetal membranes than IL-6. / Fortunato, S. J.; Menon, Ramkumar.
In: Placenta, Vol. 24, No. 10, 11.2003, p. 922-928.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - IL-1β is a better inducer of apoptosis in human fetal membranes than IL-6
AU - Fortunato, S. J.
AU - Menon, Ramkumar
PY - 2003/11
Y1 - 2003/11
N2 - The objective of this study was to compare two of the inflammatory cytokines (IL-1 and IL-6) elevated in both preterm labour and preterm premature rupture of the membranes (pPROM), with respect to their ability to induce fetal membrane apoptosis. Fetal membranes collected from women at term were placed in an organ explant system and stimulated with recombinant human IL-1β and IL-6. The expression patterns of pro-apoptotic genes (Fas, FasL, TRADD, FADD) and caspases 2, 3, 8, 9 were studied using PCR. Caspase activity and DNA fragmentation were studied using substrate assays and TUNEL respectively. Caspase 8 and 9 expressions were induced in IL-1β and IL-6 treated amniochorion. Caspase 2 expression was seen only in IL-1β stimulated tissues. When compared to control, IL-1β increased caspase 2, 3, 8 and 9 activities, whereas IL-6 treated membranes did not exhibit a significant change. DNA fragmentation was seen in greater numbers after IL-1β treatment than after IL-6 treatment. This study demonstrates that IL-1β is a better inducer of apoptosis in normal human fetal membranes than IL-6.
AB - The objective of this study was to compare two of the inflammatory cytokines (IL-1 and IL-6) elevated in both preterm labour and preterm premature rupture of the membranes (pPROM), with respect to their ability to induce fetal membrane apoptosis. Fetal membranes collected from women at term were placed in an organ explant system and stimulated with recombinant human IL-1β and IL-6. The expression patterns of pro-apoptotic genes (Fas, FasL, TRADD, FADD) and caspases 2, 3, 8, 9 were studied using PCR. Caspase activity and DNA fragmentation were studied using substrate assays and TUNEL respectively. Caspase 8 and 9 expressions were induced in IL-1β and IL-6 treated amniochorion. Caspase 2 expression was seen only in IL-1β stimulated tissues. When compared to control, IL-1β increased caspase 2, 3, 8 and 9 activities, whereas IL-6 treated membranes did not exhibit a significant change. DNA fragmentation was seen in greater numbers after IL-1β treatment than after IL-6 treatment. This study demonstrates that IL-1β is a better inducer of apoptosis in normal human fetal membranes than IL-6.
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U2 - 10.1016/S0143-4004(03)00160-7
DO - 10.1016/S0143-4004(03)00160-7
M3 - Article
VL - 24
SP - 922
EP - 928
JO - Placenta
JF - Placenta
SN - 0143-4004
IS - 10
ER -