Evidence map›Paper›PMID 18535290›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2008

Optimized adeno-associated virus 8 produces hepatocyte-specific Cre-mediated recombination without toxicity or affecting liver regeneration.

Karen J Ho, Caroline E Bass, Alexander H K Kroemer, Chunyan Ma, Ernest Terwilliger, Seth J Karp

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Hepatocyte Specific gp130 Signalling Underlies APAP Induced Liver Injury.International journal of molecular sciences · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Alcoholic Hepatitis: Lost in Translation.Journal of clinical and translational hepatology · 2018
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. BMP4 is a novel paracrine inhibitor of liver regeneration.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Karen J HoDept. of Surgery, Beth Israel Deaconess Medical Ctr., 110 Francis St., 7th floor, Boston, MA 02215, USA.
Caroline E Bass
Alexander H K Kroemer
Chunyan Ma
Ernest Terwilliger
Seth J Karp
Harvard University Press · US

Funding

HARVARD-LONGWOOD RESEARCH TRAINING IN VASCULAR SURGERYT32HL007734 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI FERRAN, CHRISTIANE, LOGERFO, FRANK W · 1993 to 2023
$10.5M
Activin Signaling in Liver Size and RegenerationK08DK064648 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI KARP, SETH J · 2003 to 2007
$650k
RNA Interference to MAPK Events in delta9-THC ToleranceF32DA017543 · NIDA · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BASS, CAROLINE · 2003 to 2005
$143k
NHLBI NIH HHS HL007734NIDA NIH HHS F32 DA017543NIDDK NIH HHS DK064648
6 · The paper itself

Abstract

unlabelledEngineering viral vectors to produce liver-specific protein expression may help advance understanding of hepatic regeneration and disease states. In addition to introducing genes of interest to the liver, these vectors can be adapted for gene deletion when designed to express Cre recombinase. The ability to use this system requires high, liver-restricted expression, low toxicity, and no effect on the process of interest. We developed an adeno-associated virus 8 (AAV8) with a codon-optimized Cre recombinase under a hepatocyte-specific major urinary protein (MUP) promoter (MUP-iCre-AAV8) that fulfills these requirements. A single intravenous injection of ROSA26R reporter mice, which express lacZ after Cre-mediated recombination, demonstrated homogeneous beta-galactosidase expression limited to hepatocytes after only 7 days. Cre protein expression remained strong for at least 31 days. Serum liver function tests and histology demonstrated minimal liver toxicity. The presence of MUP-iCre-AAV8 did not affect hepatocyte proliferation after partial hepatectomy as measured by Ki67 staining.

conclusionAAV8 with the MUP promoter, by virtue of its lack of hepatic toxicity or effect on liver regeneration, may be an efficient alternative to complex transgenic methodologies for studies of the mouse liver.

Indexed as

Gene Transfer TechniquesRecombination, GeneticAnimalsbeta-GalactosidaseCell ProliferationDependovirusGenetic VectorsHepatocytesIntegrasesLiver RegenerationMaleMiceMice, Transgenicbeta-GalactosidaseCre recombinaseIntegrases

Identifiers

PMID18535290
PMCPMC2519860
OpenAlexW2122864343

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.