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. 2018 Jan 31;9:84–97. doi: 10.1016/j.molmet.2018.01.016

Figure 7.

Figure 7

TALK-1 KO α-cells exhibit altered Ca2+dynamics only in intact islets. (A) Recordings of intracellular Ca2+ responses in WT α-cells, in islets expressing the genetically encoded Ca2+ indicator GCaMP3 specifically in α-cells (representative of islet α-cells from N = 3 mice). (B) Recordings of intracellular Ca2+ responses in TALK-1 KO α-cells, in islets expressing the genetically encoded Ca2+ indicator GCaMP3 specifically in α-cells (representative of islet α-cells from N = 3 mice). (C) Recordings of intracellular Ca2+ responses in single WT α-cells expressing the genetically encoded Ca2+ indicator GCaMP3 (representative of α-cells from N = 3 mice). (D) Recordings of intracellular Ca2+ responses in single TALK-1 KO α-cells expressing the genetically encoded Ca2+ indicator GCaMP3 (representative of α-cells from N = 3 mice). (E and F) Comparison of percent oscillating α-cells and Ca2+ AUC determined from WT and TALK-1 KO α-cells under the indicated conditions (N = 3 mice per genotype). (G) Islets were incubated for 1 h with the indicated treatments (SSTR2 antagonist: 500 nM CYN154806); N = 10 mice per genotype (glucose only); 3 mice per genotype (+CYN154806); *P < 0.05.