“…It is clearly demonstrated and previously described that VEGF, as well as many other growth factors, utilize are able to activate neoangiogenesis utilizing Ca2+ signaling toolkit which regulates EPCs biological properties like differentiation, proliferative rate, migration and vessel tube formation. Intracellular Ca2+ signals toolkit could be manipulate to repair damaged tissue using genetically transformed cells or represent the target site of cell based therapy through the impairment of EPC-dependent vasculogenesis and adverse tumour neovascularization [ 178 , 179 , 180 , 181 , 182 , 183 , 184 , 185 , 186 , 187 , 188 , 189 , 190 , 191 , 192 ]. Also MSC are useful to reduce a lesion because they could be able to stop the process of fibrosis, apoptosis, and could be responsible to induce mitosis in intrinsic cellular progenitors [ 193 ].…”