Evidence map›Paper›PMID 31267702›Full record

ArticleJournal of tissue engineering and regenerative medicine2019

Kidney-in-a-lymph node: A novel organogenesis assay to model human renal development and test nephron progenitor cell fates.

Maria Giovanna Francipane, Bing Han, Leif Oxburgh, Sunder Sims-Lucas, Zhongwei Li, Eric Lagasse

Open access · greenAbstract read
In one paragraph

Article in Journal of tissue engineering and regenerative medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  5. FromLab on a chip · 2024
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  11. Molecular therapy. Methods & clinical development · 2020
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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 4 institutions in 2 countries.

Maria Giovanna FrancipaneMcGowan Institute for Regenerative Medicine and Pathology Department, University of Pittsburgh, Pittsburgh, Pennsylvania.ORCID 0000-0002-7194-7918
Bing HanMcGowan Institute for Regenerative Medicine and Pathology Department, University of Pittsburgh, Pittsburgh, Pennsylvania.
Leif OxburghCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine.ORCID 0000-0002-2825-7663
Sunder Sims-LucasRangos Research Center, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.
Zhongwei LiDepartment of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine of USC, Los Angeles, California, USA.
Eric LagasseMcGowan Institute for Regenerative Medicine and Pathology Department, University of Pittsburgh, Pittsburgh, Pennsylvania.
University of Pittsburgh · USCalifornia Institute for Regenerative Medicine · USChildren's Hospital of Pittsburgh · USMaine Medical Center Research Institute · US

Funding

Engineering erythropoietin-producing cellsR24DK106743 · NIDDK · ROGOSIN INSTITUTE · PI CARROLL, THOMAS JOSEPH, CLEAVER, ONDINE B · 2015 to 2019
$7.0M
Organogenesis of Ectopic Tissue in Lymph NodeR01DK085711 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAGASSE, ERIC · 2009 to 2013
$3.6M
A New Molecular Mechanism to Bioengineering a LiverR01DK114282 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAGASSE, ERIC · 2018 to 2022
$2.1M
NIDDK NIH HHS R01 DK085711NIDDK NIH HHS R01 DK114282NIDDK NIH HHS R24 DK106743
6 · The paper itself

Abstract

Stem cell-derived organoids are emerging as sophisticated models for studying development and disease and as potential sources for developing organ substitutes. Unfortunately, although organoids containing renal structures have been generated from mouse and human pluripotent stem cells, there are still critical unanswered questions that are difficult to attain via in vitro systems, including whether these nonvascularized organoids have a stable and physiologically relevant phenotype or whether a suitable transplantation site for long-term in vivo studies can be identified. Even orthotopic engraftment of organoid cultures in the adult does not provide an environment conducive to vascularization and functional differentiation. Previously, we showed that the lymph node offers an alternative transplantation site where mouse metanephroi can differentiate into mature renal structures with excretory, homeostatic, and endocrine functions. Here, we show that the lymph node lends itself well as a niche to also grow human primary kidney rudiments and can additionally be viewed as a platform to interrogate emerging renal organoid cultures. Our study has a wide-ranging impact for tissue engineering approaches to rebuild functional tissues in vivo including-but not limited to-the kidney.

Indexed as

Models, BiologicalOrganogenesisAnimalsHumansLymph NodesMice, Inbred BALB CMice, NudeNephronsStem Cellsbioreactorfunctional maturationkidney engineeringkidney organogenesislymph nodenephron progenitors

Identifiers

PMID31267702
PMCPMC7099580
OpenAlexW2954251825

What OpenQuestion holds

Textmetadata
LicenceTDM
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.