Journal article
Hepatocyte DNA replication in growing liver requires either glutathione or a single allele of txnrd1
Free radical biology & medicine, Vol.52(4), pp.803-810
02/15/2012
Handle:
https://hdl.handle.net/2376/108711
PMCID: PMC3267845
PMID: 22198266
Abstract
Ribonucleotide reductase (RNR) activity requires an electron donor, which in bacteria, yeast, and plants is usually either reduced thioredoxin (Trx) or reduced glutaredoxin. Mice lacking glutathione reductase are viable and, although mice lacking thioredoxin reductase 1 (TrxR1) are embryonic-lethal, several studies have shown that mouse cells lacking the txnrd1 gene, encoding TrxR1, can proliferate normally. To better understand the in vivo electron donor requirements for mammalian RNR, we here investigated whether replication of TrxR1-deficient hepatocytes in mouse livers either employed an alternative source of Trx-reducing activity or, instead, solely relied upon the glutathione (GSH) pathway. Neither normal nor genetically TrxR1-deficient livers expressed substantial levels of mRNA splice forms encoding cytosolic variants of TrxR2, and the TrxR1-deficient livers showed severely diminished total TrxR activity, making it unlikely that any alternative TrxR enzyme activities complemented the genetic TrxR1 deficiency. To test whether the GSH pathway was required for replication, GSH levels were depleted by administration of buthionine sulfoximine (BSO) to juvenile mice. In controls not receiving BSO, replicative indexes were similar in hepatocytes having two, one, or no functional alleles of txnrd1. After BSO treatment, hepatocytes containing either two or one copies of this gene were also normal. However, hepatocytes completely lacking a functional txnrd1 gene exhibited severely reduced replicative indexes after GSH depletion. We conclude that hepatocyte proliferation in vivo requires either GSH or at least one functional allele of txnrd1, demonstrating that either the GSH- or the TrxR1-dependent redox pathway can independently support hepatocyte proliferation during liver growth.
► Mouse hepatocytes genetically lacking TrxR1 exhibit normal proliferation rates. ► Cytosolic variants of TrxR2 do not functionally replace TrxR1 in txnrd1-null livers. ► Wild-type hepatocytes lacking GSH proliferate normally. ► Hepatocytes lacking both TrxR1 and GSH exhibit severely reduced replication. ► S-phase DNA replication in hepatocytes requires either TrxR1 or GSH.
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Details
- Title
- Hepatocyte DNA replication in growing liver requires either glutathione or a single allele of txnrd1
- Creators
- Justin R Prigge - Department of Immunology and Infectious Disease, Montana State University, Bozeman, MT 59718, USASofi Eriksson - Division of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, SwedenSonya V Iverson - Department of Immunology and Infectious Disease, Montana State University, Bozeman, MT 59718, USATesia A Meade - Biomedical Engineering Program, Case Western Reserve University, Cleveland, OH 44106, USAMario R Capecchi - Howard Hughes Medical Institute, University of Utah, Salt Lake City, UT 84112, USAElias S.J Arnér - Division of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, SwedenEdward E Schmidt - Department of Immunology and Infectious Disease, Montana State University, Bozeman, MT 59718, USA
- Publication Details
- Free radical biology & medicine, Vol.52(4), pp.803-810
- Academic Unit
- UNKNOWN
- Publisher
- Elsevier Inc
- Identifiers
- 99900547239901842
- Language
- English
- Resource Type
- Journal article