Evidence map›Paper›PMID 7597042›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1995

Integration of transplanted hepatocytes into host liver plates demonstrated with dipeptidyl peptidase IV-deficient rats.

S Gupta, P Rajvanshi, C D Lee

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 139 citations in OpenAlex.

  1. Article
  2. Article
  3. InGene expression · 2018
    Article
  4. Article
  5. Review
  6. Cell and tissue engineering for liver disease.Science translational medicine · 2014
    Review
  7. Cell therapy to remove excess copper in Wilson's disease.Annals of the New York Academy of Sciences · 2014
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. A growth-constrained environment drives tumor progression invivo.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  14. Article
  15. Article
  16. Differentiation of pancreatic epithelial progenitor cells into hepatocytes following transplantation into rat liver.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  17. 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

3 authors at 1 institution in 1 country.

S GuptaMarion Bessin Liver Research Center, Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461-1602, USA.
P Rajvanshi
C D Lee
Yeshiva University · US

Funding

LIVER REPOPULATION FOR LIVER INJURY AND GENE THERAPYR01DK046952 · NIDDK · YESHIVA UNIVERSITY · PI GUPTA, SANJEEV · 1994 to 2007
$3.5M
GROWTH FACTORS AND LIVER REGENERATIONK08DK001909 · NIDDK · YESHIVA UNIVERSITY · PI GUPTA, SANJEEV · 1989 to 1993
–
NIDDK NIH HHS DK-K08-01909NIDDK NIH HHS R01 DK46952PHS HHS P30-41296
6 · The paper itself

Abstract

To analyze mechanisms of liver repopulation, we transplanted normal hepatocytes into syngeneic rats deficient in dipeptidyl peptidase IV activity. When isolated hepatocytes were injected into splenic pulp, cells promptly migrated into hepatic sinusoids. To examine whether transplanted hepatocytes entered liver plates and integrated with host hepatocytes, we analyzed sharing of hepatocyte-specific gap junctions and bile canaliculi. Colocalization studies showed gap junctions uniting adjacent transplanted and host hepatocytes in liver plates. Visualization of bile canalicular domains in transplanted and host hepatocytes with dipeptidyl peptidase IV and ATPase activities, respectively, demonstrated hybrid bile canaliculi, which excreted a fluorescent conjugated bile acid analogue. These results indicate that transplanted hepatocytes swiftly overcome mechanical barriers in hepatic sinusoids to enter liver plates and join host cells. Integration into liver parenchyma should physiologically regulate the function or disposition of transplanted hepatocytes and benefit applications such as gene therapy.

Indexed as

Adenosine TriphosphatasesAnimalsBile CanaliculiCell TransplantationDipeptidyl Peptidase 4Gap JunctionsImmunohistochemistryLiverMicroscopy, FluorescenceRatsRats, Inbred F344Reference ValuesTransplantation, IsogeneicAdenosine TriphosphatasesDipeptidyl Peptidase 4

Identifiers

PMID7597042
PMCPMC41601
OpenAlexW1992201379

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.