Abstract
Summary
Parallel studies of 3H-TdR and 125I-UdR incorporation into regenerating liver following repeated injection into female Swiss albino mice yielded the following results: (i) both 3H-TdR and 125I-UdR are reutilized, although 3H-TdR to a considerably greater extent; (ii) in addition to local reutilization, the data are explained by labeled precursors entering the regenerating liver from the intestine via the portal circulation. Precursor supply from immigrated leukocytes also occurs; and (iii) since a bypass of the thymidine kinase salvage pathway is unlikely, the incorporation of tracer into the regenerating liver must occur from the nucleoside level.
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