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. 2019 Feb 20;24(5):453–464. doi: 10.1007/s10495-019-01528-w

Fig. 1.

Fig. 1

Schematic of immunophenotyping of RCD. Live (including early apoptotic) and dead (including late apoptotic) cells were gated from a Zombie NIR vs. Caspase-3-BV650 dot-plot (a). Live and dead necroptotic cells were defined as Caspase-3− ve/RIP3high + ve, early or late apoptotic (Caspase-3+ ve/RIP3− ve), RIP1-dependent apoptotic (RIP1-APO, Caspase-3+ ve/RIP3+ ve) and Double Negative (DN, Caspase-3− ve/RIP3− ve) (b, c). Then each of these live and dead cell populations were then gated on a H2AX vs. PARP dot-plots to show the incidence of DDR (H2AX+ ve/PARP− ve), hyper-activation of PARP (H2AX+ ve/PARP+ ve), parthanatos (H2AX− ve/PARP+ ve) and QN (H2AX− ve/PARP− ve), (d, e)