Evidence map›Paper›PMID 35100814›Full record

ReviewAmerican journal of physiology. Renal physiology2022

Potential renal stem/progenitor cells identified by in vivo lineage tracing.

Wenzheng Zhang, Chao Gao, Akaki Tsilosani, Rohan Samarakoon, Robert Plews, Paul J Higgins

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Renal physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Formation of the glomerular microvasculature is regulated by VEGFR-3.American journal of physiology. Renal physiology · 2023
    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.

Wenzheng ZhangDepartment of Regenerative and Cancer Cell Biology, Albany Medical College, Albany, New York.
Chao GaoDepartment of Regenerative and Cancer Cell Biology, Albany Medical College, Albany, New York.
Akaki TsilosaniDepartment of Regenerative and Cancer Cell Biology, Albany Medical College, Albany, New York.
Rohan SamarakoonDepartment of Regenerative and Cancer Cell Biology, Albany Medical College, Albany, New York.
Robert PlewsDepartment of General Surgery, Albany Medical College, Albany, New York.
Paul J HigginsDepartment of Regenerative and Cancer Cell Biology, Albany Medical College, Albany, New York.ORCID 0000-0001-5208-1197
Albany Medical Center Hospital · US

Funding

Epigenic Control of ENaC Transcription and Sodium TransportR01DK080236 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ZHANG, WENZHENG · 2009 to 2016
$2.2M
NIDDK NIH HHS R01 DK080236
6 · The paper itself

Abstract

Mammalian kidneys consist of more than 30 different types of cells. A challenging task is to identify and characterize the stem/progenitor subpopulations that establish the lineage relationships among these cellular elements during nephrogenesis in the embryonic and neonate kidneys and during tissue homeostasis and/or injury repair in the mature kidney. Moreover, the potential clinical utility of stem/progenitor cells holds promise for the development of new regenerative medicine approaches for the treatment of renal diseases. Stem cells are defined by unlimited self-renewal capacity and pluripotentiality. Progenitor cells have pluripotentiality but no or limited self-renewal potential. Cre-LoxP-based in vivo genetic lineage tracing is a powerful tool to identify stem/progenitor cells in their native environment. Hypothetically, this technique enables investigators to accurately track the progeny of a single cell or a group of cells. The Cre/LoxP system has been widely used to uncover the function of genes in various mammalian tissues and to identify stem/progenitor cells through in vivo lineage tracing analyses. In this review, we summarize the recent advances in the development and characterization of various Cre drivers and their use in identifying potential renal stem/progenitor cells in both developing and mature mouse kidneys.

Indexed as

KidneyStem CellsAnimalsCell DifferentiationCell LineageHomeostasisMammalsMiceOrganogenesisCre-LoxP systemdevelopmentin vivo lineage tracingregenerationrenal stem/progenitor cells

Identifiers

PMID35100814
PMCPMC8934668
OpenAlexW4210264308

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.