s of the protocol were described previously. The initial protocol was aimed at studying the interaction of H. pylori infection and low dose aspirin. Briefly, human healthy volunteers were stratified accord ing to the H. pylori status leading to the H. pylori posi tive and negative group. After Regorafenib cost successful eradication therapy, 9 out of 10 H. pylori infected individuals agreed to participate in this study after 3 months again composing the H. pylori eradicated group. In order to investigate the potential interaction between Progranulin and SLPI, mucosal and serum levels as well as gene expression levels of Progranulin were analyzed retro spectively in existing samples and tissue specimens in relation to H. pylori status and SLPI expression levels published previously.

The analysis of Progranulin expression was performed in the pre treatment sam ples, which correspond to day 0 before low dose aspirin was taken by the individuals. The study includes a correlation analysis of mucosal Progranulin levels with those of SLPI studied in the same cohorts previously, details concerning the analysis of SLPI were reported recently. Determination of Progranulin expression quantitative RT PCR and ELISA Progranulin levels were quantified in the total protein extract from mucosal biopsies at sera stored at 80 C in previous study. Progranulin levels were quantified using the Progranulin ELISA kit as described by the manufacturer. Protein levels were normalized to ng ug total protein content of extracted mucosal samples or ng ml for sera.

Corresponding Progranulin m RNA levels were deter mined Drug_discovery by quantitative RT PCR using existing cDNA samples stored at 80 C. Quantitative RT PCR was per formed using an iCycler and HotStarTaq Master Mix as described. Initial activation of Taq polymerase at 95 C for 15 min was followed by 40 cycles with dena turation at 94 C for 30 s, annealing at 60 C for 30 s and elongation at 72 C for 30 s. The fluorescence intensity of the double strand specific SYBR Green I, reflecting the amount of actually formed PCR product, was read real time at the end of each elongation step. Then spe cific initial template mRNA amounts were calculated by determining the time point at which the linear increase of sample PCR product started, relative to the corre sponding points of a standard curve, these are given as arbitrary units.

Both PCR products were cloned into the pDIRECT, and subsequent dilutions of the corresponding plasmid DNA were used to create a standard curve for the RT PCR. The correlation coefficients of both Progranulin and b actin standards were 0. 95. b actin mRNA amounts were used to normalize the cDNA contents of the different samples. Final data despite reflect the ratio in a. u. between Progranulin transcript and b actin transcript levels. The following primers were used for the RT PCR analysis, ? actin, and Progranulin. Both cDNA fragments included intron spanning regions resulting in the generation of a larger PCR product from genomic DNA o