Publication Date:
2015
Short description:
PKCε is a negative regulator of PVAT-derived vessel formation / Galli, D., Carubbi, C., Masselli, E., Corradi, D., DEI CAS, A., Nouvenne, A., Bucci, G., Arcari, M.L., Mirandola, P., Vitale, M., Gobbi, G.. - In: EXPERIMENTAL CELL RESEARCH. - ISSN 0014-4827. - 330:2(2015), pp. 277-286. [10.1016/j.yexcr.2014.11.011]
abstract:
Rationale: Vessel formation is a crucial event in tissue repair after injury. Thus, one assumption of innovative therapeutic approaches is the understanding of its molecular mechanisms. Notwithstanding our knowledge of the role of Protein Kinase C epsilon (PKC epsilon) in cardio-protection and vascular restenosis, its role in vessel progenitor differentiation remains elusive.
Objective: Given the availability of PKC epsilon pharmacological modulators already tested in clinical trials, the specific aim of this study is to unravel the role of PKC epsilon in vessel progenitor differentiation, with implications in vascular pathology and vasculogenesis.
Methods and results: Mouse Pen-Vascular Adipose Tissue (PVAT) was used as source of mesenchymal vessel progenitors. VEGF-induced differentiation of PVAT cells down-regulates both PKC epsilon and p-PAK1 protein expression levels. PKC epsilon overexpression and activation: i) reduced the expression levels of SMA and PECAM in endothelial differentiation of PVAT cells; ii) completely abrogated tubules formation in collagen gel assays; iii) increased the expression of p-PAK1.
Conclusion: PKC epsilon negatively interferes with vessel progenitor differentiation via interaction with PAK-1.
Objective: Given the availability of PKC epsilon pharmacological modulators already tested in clinical trials, the specific aim of this study is to unravel the role of PKC epsilon in vessel progenitor differentiation, with implications in vascular pathology and vasculogenesis.
Methods and results: Mouse Pen-Vascular Adipose Tissue (PVAT) was used as source of mesenchymal vessel progenitors. VEGF-induced differentiation of PVAT cells down-regulates both PKC epsilon and p-PAK1 protein expression levels. PKC epsilon overexpression and activation: i) reduced the expression levels of SMA and PECAM in endothelial differentiation of PVAT cells; ii) completely abrogated tubules formation in collagen gel assays; iii) increased the expression of p-PAK1.
Conclusion: PKC epsilon negatively interferes with vessel progenitor differentiation via interaction with PAK-1.
Iris type:
1.1 Articolo in rivista
Keywords:
Differentiation; Peri-Vascular Adipose Tissue; PKCε; Vascular progenitor; Actins; Adipose Tissue; Adventitia; Animals; Antigens; CD31; Calcium-Binding Proteins; Cell Differentiation; Cells; Cultured; Coronary Restenosis; Down-Regulation; Endothelial Cells; Enzyme Activation; Mice; Microfilament Proteins; Myocytes; Cardiac; Neovascularization; Physiologic; Protein Kinase C-epsilon; Smad Proteins; Vascular Endothelial Growth Factor A; p21-Activated Kinases; Cell Biology; Medicine (all)
List of contributors:
Galli, Daniela; Carubbi, Cecilia; Masselli, Elena; Corradi, Domenico; DEI CAS, Alessandra; Nouvenne, Antonio; Bucci, Giovanna; Arcari, Maria Luisa; Mirandola, Prisco; Vitale, Marco; Gobbi, Giuliana
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