Evidence map›Paper›PMID 16007252›Full record

ArticleThe Journal of clinical investigation2005

Intrarenal cells, not bone marrow-derived cells, are the major source for regeneration in postischemic kidney.

Fangming Lin, Ashley Moran, Peter Igarashi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed
13.9field-weighted citation impact, top 1% 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

142 citing papers in PubMed, 424 citations in OpenAlex.

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  13. Magnetic FeCell proliferation · 2021
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Cell Cycle Dysregulation and Renal Fibrosis.Frontiers in cell and developmental biology · 2021
    Review
  19. Kidney regeneration approaches for translation.World journal of urology · 2020
    Review
  20. The Effect of Shen Qi Wan Medicated Serum on NRK-52E Cells Proliferation and Migration by Targeting Aquaporin 1 (AQP1).Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article

82 more citing papers are in PubMed but not listed here.

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.

Fangming LinDepartment of Pediatrics and Department of Internal Medicine and Division of Basic Sciences, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 5390-9063, USA. Fangming.lin@utsouthwestern.edu
Ashley Moran
Peter Igarashi
Southwestern Medical Center · US

Funding

Epithelial Cell Linage in the Kidney and GU TractR01DK066535 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI IGARASHI, PETER · 2004 to 2007
$1.1M
STEM CELL THERAPY IN ACUTE RENAL FAILUREK08DK062839 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI LIN, FANGMING · 2003 to 2007
$621k
NIDDK NIH HHS DK062839NIDDK NIH HHS DK066535NIDDK NIH HHS K08 DK062839NIDDK NIH HHS R01 DK066535
6 · The paper itself

Abstract

Ischemic injury to the kidney produces acute tubular necrosis and apoptosis followed by tubular regeneration and recovery of renal function. Although mitotic cells are present in the tubules of postischemic kidneys, the origins of the proliferating cells are not known. Bone marrow cells (BMCs) can differentiate across lineages to repair injured organs, including the kidney. However, the relative contribution of intrarenal cells and extrarenal cells to kidney regeneration is not clear. We produced transgenic mice that expressed enhanced GFP (EGFP) specifically and permanently in mature renal tubular epithelial cells. Following ischemia/reperfusion injury (IRI), EGFP-positive cells showed incorporation of BrdU and expression of vimentin, which provides direct evidence that the cells composing regenerating tubules are derived from renal tubular epithelial cells. In BMC-transplanted mice, 89% of proliferating epithelial cells originated from host cells, and 11% originated from donor BMCs. Twenty-eight days after IRI, the kidneys contained 8% donor-derived cells, of which 8.4% were epithelial cells, 10.6% were glomerular cells, and 81% were interstitial cells. No renal functional improvement was observed in mice that were transplanted with exogenous BMCs. These results show that intrarenal cells are the main source of renal repair, and a single injection of BMCs does not make a significant contribution to renal functional or structural recovery.

Indexed as

RegenerationAnimalsBone Marrow CellsBone Marrow TransplantationCell DifferentiationEpithelial CellsFemaleGreen Fluorescent ProteinsIn Situ Hybridization, FluorescenceKidneyKidney TubulesMaleMiceMice, Inbred C57BLMice, TransgenicRecombinant Proteinsenhanced green fluorescent proteinGreen Fluorescent ProteinsRecombinant Proteins

Identifiers

PMID16007252
PMCPMC1159127
OpenAlexW2166234655

What OpenQuestion holds

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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.