Figure 4
Figure 4. The proximal region and tyrosine residue 338 of IL-2Rβ A region are crucial for lineage conversion. (A) Illustration of deletion chimeric receptors. IL-2Rβ A region was divided into 2 sub-regions (a.a. 313-353 [proximal] and a.a. 354-382 [distal]). (B) The chimeric receptors shown in panel A were retrovirally introduced into CLPs. The lineage conversion ability of each chimeric receptor was examined by myeloid colony forming ability in methylcellulose culture in the presence of IL-3 and GM-CSF. (C) Diagram of tyrosine-to-phenylalanine mutants. The individual tyrosine (Y) residues within IL-2Rβ A region were mutated into phenylalanine (F). (D) Lineage conversion ability was assessed with the methylcellulose culture as described for panel B. (B,D) Error bars represent standard deviation from triplicate samples.

The proximal region and tyrosine residue 338 of IL-2Rβ A region are crucial for lineage conversion. (A) Illustration of deletion chimeric receptors. IL-2Rβ A region was divided into 2 sub-regions (a.a. 313-353 [proximal] and a.a. 354-382 [distal]). (B) The chimeric receptors shown in panel A were retrovirally introduced into CLPs. The lineage conversion ability of each chimeric receptor was examined by myeloid colony forming ability in methylcellulose culture in the presence of IL-3 and GM-CSF. (C) Diagram of tyrosine-to-phenylalanine mutants. The individual tyrosine (Y) residues within IL-2Rβ A region were mutated into phenylalanine (F). (D) Lineage conversion ability was assessed with the methylcellulose culture as described for panel B. (B,D) Error bars represent standard deviation from triplicate samples.

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