Sequential control of myeloid cell proliferation and differentiation by cytokine receptor-based chimeric antigen receptors.
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ABSTRACT: As chimeric antigen receptor (CAR)-T cell therapy has been recently applied in clinics, controlling the fate of blood cells is increasingly important for curing blood disorders. In this study, we aim to construct proliferation-inducing and differentiation-inducing CARs (piCAR and diCAR) with two different antigen specificities and express them simultaneously on the cell surface. Since the two antigens are non-cross-reactive and exclusively activate piCAR or diCAR, sequential induction from cell proliferation to differentiation could be controlled by switching the antigens added in the culture medium. To demonstrate this notion, a murine myeloid progenitor cell line 32Dcl3, which proliferates in an IL-3-dependent manner and differentiates into granulocytes when cultured in the presence of G
SUBMITTER: Nakajima K
PROVIDER: S-EPMC9794043 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature
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