TY - JOUR
T1 - Does leptin exhibit cytokine-like properties in tissues of pregnancy?
AU - Soh, EBE
AU - Mitchell, MD
AU - Keelan, Jeffrey
PY - 2000
Y1 - 2000
N2 - PROBLEM: To determine whether leptin exhibits cytokine-like properties in gestational tissues in light of its homologies with the class I family of cytokines.METHOD OF STUDY: WISH and JEG3 cells, and amnion and choriodecidua explants, were treated inflammatory modulators (interleukin-1 beta [IL-1 beta], tumor necrosis faetor-alpha [TNF-alpha] and bacterial lipupolysaccharide [LPS]) and leptin production was measured by immunoassay. Other agents known to regulate adipocyte leptin production were also tested for comparative purposes. In addition, WISH cells, JAR cells and placental explants were treated with leptin to assess its effects on production of IL-8, IL-6 and prostaglandin E-2 (PGE(2)).RESULTS: Leptin production by all cells and tissues studied was unaffected by treatment with IL-1 beta (2.5 ng/mL), TNF-alpha (25 ng/mL) and LPS (2.5 mu g/mL). Dexamethasone stimulated leptin production over two-fold by WISH and JEG3 cells, whereas insulin also stimulated a two-fold increase in leptin production in JEG3 cells. IL-6 production by JAR cells and placental explants was stimulated (two- to three-fold) by leptin (300 ng/mL). PGE(2) production was unaffected.CONCLUSIONS: Leptin derived from gestational tissues is unlikely to play a role in inflammatory reactions within the placenta, but may regulate placental cytokine production. The physiological significance of amnion-derived leptin remains to be established.
AB - PROBLEM: To determine whether leptin exhibits cytokine-like properties in gestational tissues in light of its homologies with the class I family of cytokines.METHOD OF STUDY: WISH and JEG3 cells, and amnion and choriodecidua explants, were treated inflammatory modulators (interleukin-1 beta [IL-1 beta], tumor necrosis faetor-alpha [TNF-alpha] and bacterial lipupolysaccharide [LPS]) and leptin production was measured by immunoassay. Other agents known to regulate adipocyte leptin production were also tested for comparative purposes. In addition, WISH cells, JAR cells and placental explants were treated with leptin to assess its effects on production of IL-8, IL-6 and prostaglandin E-2 (PGE(2)).RESULTS: Leptin production by all cells and tissues studied was unaffected by treatment with IL-1 beta (2.5 ng/mL), TNF-alpha (25 ng/mL) and LPS (2.5 mu g/mL). Dexamethasone stimulated leptin production over two-fold by WISH and JEG3 cells, whereas insulin also stimulated a two-fold increase in leptin production in JEG3 cells. IL-6 production by JAR cells and placental explants was stimulated (two- to three-fold) by leptin (300 ng/mL). PGE(2) production was unaffected.CONCLUSIONS: Leptin derived from gestational tissues is unlikely to play a role in inflammatory reactions within the placenta, but may regulate placental cytokine production. The physiological significance of amnion-derived leptin remains to be established.
UR - https://www.scopus.com/pages/publications/0034065540
U2 - 10.1111/j.8755-8920.2000.430508.x
DO - 10.1111/j.8755-8920.2000.430508.x
M3 - Article
SN - 1046-7408
VL - 43
SP - 292
EP - 298
JO - American Journal of Reproductive Immunology
JF - American Journal of Reproductive Immunology
ER -