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Articles in PresS, published online ahead of print October 16, 2002
Am J Physiol Gastrointest Liver Physiol, 10.1152/ajpgi.00175.2002
Submitted on May 14, 2002
Accepted on October 7, 2002
knockout mice following partial hepatectomy
1 Department of Pharmacology, University of North Carolina, Chapel Hill, North Carolina, USA; Curriculum in Toxicology, University of North Carolina, Chapel Hill, North Carolina, USA
2 Department of Pharmacology, University of North Carolina, Chapel Hill, North Carolina, USA
* To whom correspondence should be addressed. E-mail: wheelmi{at}med.unc.edu.
Liver regeneration following partial hepatectomy (PH)) involves several signaling mechanisms including activation of the small GTPases Ras and RhoA in response to mitogens, leading to DNA synthesis and cell proliferation. Peroxisome proliferator activated receptor alpha (PPAR
) regulates the expression of several key enzymes in isoprenoid synthesis, key events for membrane association of Ras and RhoA. Thus, the role of PPAR in cell proliferation following PH was tested. Following PH, an increase in PPAR DNA binding was observed in wild-type mice, correlating with an increase the PPAR-regulated enzyme acyl CoA oxidase. In addition, the PPAR regulated genes farnesyl pyrophosphate synthase and HMG-CoA synthase were significantly increased in wild-type mice. However these increases were not observed in PPAR knockout mice. The peak in DNA synthesis observed 42 hours after PH was reduced by ~ 60% in PPAR deficient mice, despite increases in TNF and IL-1. Also, under these conditions, membrane association of Ras was high in wild-type mice after PH but was impaired in PPAR-/- mice. Accordingly, Ras was significantly elevated in the cytosol in
PPAR-/- mice. This observation correlated with lower levels of active GTP-bound Ras after PH in PPAR -/- mice compared to wild-type mice. Similar observations were made for RhoA. Moreover, deletion of PPAR blunted the activation of cdk2/cyclinE and cdk4/cyclinD complexes. Collectively, these results support the hypothesis that PPAR is necessary for cell cycle progression in regenerating mouse liver via mechanisms involving prenylation of small GTPases Ras and RhoA.
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