2004
DOI: 10.1016/j.jhep.2004.04.020
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Colonization of albumin-producing hepatocytes derived from transplanted F344 rat bone marrow cells in the liver of congenic Nagase's analbuminemic rats

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Cited by 18 publications
(28 citation statements)
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References 31 publications
(23 reference statements)
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“…Arikura and his colleagues [25] immediately injected normal BM-MSCs through the portal vein after 70% partial hepatectomy of albumin-deficient rats. Four weeks after the injections, the expression of albumin mRNA and protein was seen in the liver of the albumin-deficient rats.…”
Section: Discussionmentioning
confidence: 99%
“…Arikura and his colleagues [25] immediately injected normal BM-MSCs through the portal vein after 70% partial hepatectomy of albumin-deficient rats. Four weeks after the injections, the expression of albumin mRNA and protein was seen in the liver of the albumin-deficient rats.…”
Section: Discussionmentioning
confidence: 99%
“…FAH (−/−) mouse is an animal model of fatal hereditary tyrosinemia type I, when this model was irradiated followed by transplantation with unfractionated BMSCs or purified HSCs, both of which can give rise to hepatocytes, tyrosinemia can be improved [37]. Nagase analbuminemic rats (F344alb) is an inherited model for albumin production deficiency, when BMSCs from wild-type rats were infused via the portal vein into the F344alb model pretreated with 70% hepatectomy, clusters of alb+ hepatocytes and albumin mRNA were detected in recipient liver, with elevated serum albumin level [69]. These two independent experiments indicate the BMSCs can be applied in the correction of inherited liver diseases.…”
Section: Gene Therapymentioning
confidence: 99%
“…Clusters of albumin positive Fig. 2 Potential delivery approaches of bone marrow stem cells for liver diseases hepatocytes were detected in livers of the recipients, indicating that BMSCs infusion via portal vein can increase clusters of albumin-producing hepatocytes within the liver of analbuminemic rats [69].…”
Section: Portal Vein Injectionmentioning
confidence: 99%
“…Our previous studies have demonstrated that the transplantation model using Fischer 344 rats (F344) and F344 congenic Nagase's analbuminemic rats (F344alb) to be useful for the efficiency of repopulation of the hepatocytes after HT-Tx and BM-Tx in the liver [4,25,26]. F344alb have the genetic background of F344 and are otherwise normal except for a seven base pair deletion downstream of the exon H splice site within the ninth intron of albumin gene, which leads to the inability of hepatocytes to produce albumin [27].…”
Section: Introductionmentioning
confidence: 99%