02.10.2015 Views

studies

2015SupplementFULLTEXT

2015SupplementFULLTEXT

SHOW MORE
SHOW LESS
  • No tags were found...

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

364A AASLD ABSTRACTS HEPATOLOGY, October, 2015<br />

minimal and discordant, the aims of our study were to: 1)<br />

investigate HPSE expression in HSCs during their activation;<br />

2) evaluate HPSE activity in the plasma of patients with liver<br />

fibrosis. Methods. HSCs were isolated from rat liver and cultured<br />

on plastic to induce activation. HPSE expression, together<br />

with markers of HSCs transdifferentiation, were evaluated by<br />

real-time PCR at different days after isolation. HPSE protein<br />

amount was evaluated by immunofluorescence (IF). Utilizing<br />

an ELISA method, HPSE activity was measured in the plasma<br />

from 15 healthy subjects and 45 patients diagnosed with autoimmune<br />

chronic liver diseases (15 AIH, 17 PBC, 13 PSC);<br />

HPSE activity was correlated with fibrosis staging assessed by<br />

elastography. Results. After 15 days on plastic, HSCs resulted<br />

activated with the increase of alpha-SMA, fibronectin and TGFbeta<br />

expression with respect to 7 days cultured cells. Upon activation,<br />

HPSE mRNA was significantly 1.94-fold overexpressed<br />

in 15 days vs 7 days cultured cells. HPSE increase was confirmed<br />

by IF. HPSE plasma activity was significantly higher in<br />

patients with mild, significant and severe fibrosis compared<br />

to the control group (0.32±0.04, 0.25±0.03, 0.21±0.03<br />

respectively vs 0.06±0.01, p

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!