Fig. 6.
Fig. 6. Distribution of WASPbright and WASPdim cells of the patient examined by flow cytometry. / (A) Isolated PBMCs were surface stained with marker antibodies to CD3 and CD45RA or CD19 prior to intracellular staining with 5A5 mAb. Note that the CD3+ cells consist of both WASPbrightand WASPdim cells. All WASPdim cells are within the CD3+CD45RA+ (naive) populations, whereas CD3+CD45RA− cells are only WASPbright. B cells (CD19+) are largely WASPdim. Open histograms indicate isotype control; closed histograms, WASP staining. (B) PBMCs were activated with OKT3 mAb, anti-CD28 mAb, and rIL-2 for 3 days, expanded with rIL-2 for 9 days, and stained as in panel A. Note that only WASPbrightCD3+CD45RA− were present after activation. (C) X chromosome inactivation of freshly isolated PBMCs (left) and T cells after activation in vitro (right). Note that in vitro activated T cells have paternal (wild-type) X chromosome as active. H indicatesHpaII + RsaI digest; R, RsaI digest.

Distribution of WASPbright and WASPdim cells of the patient examined by flow cytometry.

(A) Isolated PBMCs were surface stained with marker antibodies to CD3 and CD45RA or CD19 prior to intracellular staining with 5A5 mAb. Note that the CD3+ cells consist of both WASPbrightand WASPdim cells. All WASPdim cells are within the CD3+CD45RA+ (naive) populations, whereas CD3+CD45RA cells are only WASPbright. B cells (CD19+) are largely WASPdim. Open histograms indicate isotype control; closed histograms, WASP staining. (B) PBMCs were activated with OKT3 mAb, anti-CD28 mAb, and rIL-2 for 3 days, expanded with rIL-2 for 9 days, and stained as in panel A. Note that only WASPbrightCD3+CD45RA were present after activation. (C) X chromosome inactivation of freshly isolated PBMCs (left) and T cells after activation in vitro (right). Note that in vitro activated T cells have paternal (wild-type) X chromosome as active. H indicatesHpaII + RsaI digest; R, RsaI digest.

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