Publications by authors named "M Pieraggi"

Graft vascular disease (GVD) remains the major limitation to long-term survival after solid organ transplantation. Aortic or carotid allografts in rats have been shown to be useful models because similar changes to those observed in man develop within weeks. Both immunological and non-immunological factors influence the process of GVD and a method that could permit rapid multiple arterial allotransplantation in the rat would be of great value.

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Article Synopsis
  • Recent studies indicate that nuclear polyphosphoinositide metabolism is linked to cell growth and differentiation, but there's limited knowledge about how these processes are regulated by PI3K in the nucleus.
  • The research shows that GTP-binding proteins can directly enhance the production of phosphatidylinositol 3,4,5-trisphosphate (PtdIns(3,4,5)P(3)) in the nucleus of pig aorta smooth muscle cells, particularly through the action of GTPgammaS.
  • Findings also suggest that a G protein-activated PI3K exists in the nucleus, which might play a crucial role in regulating smooth muscle cell proliferation and could be significant in diseases related to vascular proliferation.
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In addition to their actions on reproductive function, estrogens have important effects on endothelial cells. The present study was designed to evaluate the mechanism(s) by which 17beta-estradiol (E2) promotes endothelial cell proliferation. The potential involvement of vascular endothelial growth factor (VEGF) was investigated by the coadministration of polyclonal anti-VEGF antibody.

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The microscopic, electron microscopic and immunohistochemical observation of biopsy specimens taken at an early stage, at close and regular intervals (every 4 hours), from open skin wounds created in the pig and the monkey, together with quantitative analysis of the various cell types in the granulation tissue, supports the conception that the activated fibrocyte (fibroblast) originates from the fibrocyte of the wound edges and thus completes some earlier experimental studies. We describe here the various stages of the differentiation of the wound edge fibrocyte into an activated fibrocyte and its proliferation and migration from the edges to the site of the wound. This does not exclude the possibility that local mesenchymal cells take part in the formation of activated fibrocytes.

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