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. Author manuscript; available in PMC: 2010 Oct 20.
Published in final edited form as: Calcif Tissue Int. 2003 Sep 10;73(6):565–574. doi: 10.1007/s00223-002-0023-z

Table 1.

Effects of vehicle or 17 β-estradiol (E2) pretreatment on hOB cell conversion of 1-[14C]arachidonic acid into prostaglandinsa

Treatment PGE2, %b 6-keto-PGFb1α, %
Control 2.8 ± 0.3 1.9 ± 0.2
Control + E2 2.4 ± 0.4 1.5 ± 0.3
TGFβ 10.3 ± 2.3 2.8 ± 0.2
TGFβ + E2 9.1 ± 1.6 2.6 ± 0.3
TNF 10.9 ± 2.3 2.7 ± 0.4
TNF + E 2 9.6 ± 1.5 2.5 ± 0.4
TGFβ + TNF 27.6 ± 2.4 2.7 ± 0.4
TGFβ + TNF + E2 28.6 ± 2.9 2.7 ± 0.4
a

hOB cells were incubated for 48 hours with vehicle (0.1% ethanol) or with 17 β-estradiol (E2 ), and then stimulated with the cytokines, as indicated, for 24 hours. The conditioned media were collected and individual prostaglandins were separated by TLC.

b

Data are calculated as the % cpm of individual prostaglandin bands vs. the total cpm of the scraped and scintillation-counted TLC lane. Each of the cytokine treatments stimulated product (PGE2, 6-keto-PGF1α) formation, irrespective of 17 β-E2 pretreatment (p ≤ 0.05)