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. Author manuscript; available in PMC: 2020 Mar 2.
Published in final edited form as: RSC Adv. 2019 Oct 17;9(57):33257–33267. doi: 10.1039/c9ra05289e

Fig. 9.

Fig. 9

Reversible inhibition of respiration in the MfR. (A) Trace of reversible respiratory inhibition by KCN in adherent ARPE-19 cells cultured on MfR. Arrows – buffer flow, arrowheads – static buffer, black – RBC, gray – IBc, white arrowhead – buffer exchange artifact. (B) RO2 quantitation of the results shown in (A). Black circles – respiration buffer, gray circles – inhibition buffer. (C) Classical states of whole cell RO2 in the adherent compared to suspension MfR configuration. Respiration was in glucose, lactate, pyruvate (10, 10, 1 mM), leak was by addition of oligomycin (2.5 μM), and uncoupled RO2 was by addition of CCCP (5 μM). Squares – adherent cells, gray faded circles – suspension (from Fig. 5). RO2 were normalized to uncoupled respiration and expressed as mean ± SD (N = 3).