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The metabolism of Thy‐1 and H‐2 alloantigens was studied in murine thymocytes radiolabeled with 3 H precursors or surface radioidinated. It was found that 125 I‐labeled Thy‐1 is rapidly shed from cultured thymocytes, whereas H‐2 alloantigens are not. [ 3 H]galactose‐labeled Thy‐1 is also released from cultured thymocytes, whereas [ 3 H]leucine‐labeled H‐2 alloantigens are not. These results support the concept that H‐2 alloantigens are integral macromolecules of the plasma membrane and suggest further that Thy‐1 is a peripheral one. Possible mechanisms underlying shedding are discussed.
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Vitetta et al. (1974) studied this question.
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