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Fig. 3 | Journal of Translational Medicine

Fig. 3

From: The effect of IL-2 stimulation and treatment of TRPM3 on channel co-localisation with PIP2 and NK cell function in myalgic encephalomyelitis/chronic fatigue syndrome patients

Fig. 3

Co-localisation and immunofluorescent images of TRPM3 with PIP2 in NK cells of HC. A Example of immunostaining of PIP2 (red), nucleus (DAPI, blue), TRPM3 (green)) in an NK cell under control IL-2 conditions. Images taken using Nikon A1R + confocal microscopy. B Bar graphs represent correlation between target antigens using Pearson’s correlation coefficient and the degree of overlap between target antigens using Mander’s overlap coefficient. Co-localisation coefficients K1 (TRPM3) and K2 (PIP2) were used to determine contribution to co-localisation. Number of cells analysed are included within bar graphs: Control n = 287; PregS n = 292; and PregS + Ono n = 237. Data presented as mean ± SEM and *p < 0.05; **p < 0.01. TRPM3, transient receptor potential Melastatin; PIP2, phosphatidylinositol 4,5-bisphosphate; PregS, pregnenolone sulfate; Ono, ononetin; IL-2, interleukin 2

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