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Being the proximal tubule a major target for many nephrotoxicants, it is logical that cell-based in vitro models that seek to resemble this segment of the nephron should be characterized by the expression of important markers, including SLC22A6 (OAT1), SLC22A8 (OAT3), SLC22A2 (OCT2) on the basolateral membrane and ABCB1 (P-gp), SLC47A1 (MATE1), SLC47A2 (MATE2), ABCC2 (MRP2), ABCC4 (MRP4), ABCG2 (BCRP), and the endocytosis receptors megalin and cubilin on the apical membrane (Bajaj et al

L-NAME/L-arginine/L-NAME + L-arginine, NO-system inhibition, NO-system over-stimulation, and NO-system immobilization were simultaneously tested, and thereby, interrelated [97]

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Methods 16 , 12891296 (2019)

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