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We have determined that the brain angiotensin and HGF/c-Met systems interact in such a way that angiotensin IV (AngIV)-based analogs including Nle1-AngIV, Norleual-AngIV, Dihexa, and others influence HGF dimerization which is a prerequisite to binding at the Met receptor

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Although useful for studies of protein-mediated transport, for helping describe the contributions of specific proteins toward transcellular and paracellular solute and ion transport, and for high-throughput drug screening, [77, 78] extrapolation of data supporting the transport of microorganisms or large lipophilic molecules from cultured cells to the intact epithelium is at best hazardous