Evidence map›Paper›PMID 29928673›Full record

ArticleCellular and molecular gastroenterology and hepatology2018

Monoclonal Antibodies Reveal Dynamic Plasticity Between Lgr5- and Bmi1-Expressing Intestinal Cell Populations.

Nicholas R Smith, John R Swain, Paige S Davies, Alexandra C Gallagher, Michael S Parappilly, Catherine Z Beach, Philip R Streeter, Ian A Williamson, Scott T Magness, Melissa H Wong

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2018. 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
0.9field-weighted citation impact, top 22% 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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  9. P16Frontiers in cell and developmental biology · 2021
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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

10 authors at 2 institutions in 1 country.

Nicholas R SmithDepartment of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, Oregon.
John R SwainDepartment of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Paige S DaviesDepartment of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Alexandra C GallagherDepartment of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Michael S ParappillyDepartment of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Catherine Z BeachDepartment of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Philip R StreeterDepartment of Pediatrics, Oregon Health & Science University, Portland, Oregon.
Ian A WilliamsonDepartment of Biomedical Engineering, Department of Medicine, Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, North Carolina.
Scott T MagnessDepartment of Biomedical Engineering, Department of Medicine, Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, North Carolina.
Melissa H WongDepartment of Cell, Developmental and Cancer Biology, Oregon Health & Science University, Portland, Oregon.
Oregon Health & Science University · USUniversity of North Carolina at Chapel Hill · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI XIWEI WU · 1985 to 2026
$86.3M
Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Grace B Gill · 1997 to 2026
$60.5M
PILOT AND FEASIBILITY STUDIESP30DK034987 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Temitope O. Keku · 1985 to 2026
$30.5M
Intestinal Stem Cell Consortium Coordinating CenterU01DK085532 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI NILAND, JOYCE CAROL · 2009 to 2018
$6.5M
Training in the Molecular Basis of Skin/Mucosa PathobiologyT32CA106195 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI KULESZ-MARTIN, MOLLY F. · 2004 to 2018
$3.8M
Limited Competition for the Continuation of the Intestinal Stem Cell Consortium Coordinating CenterU24DK085532 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI NILAND, JOYCE CAROL · 2019 to 2023
$2.3M
Characterization of intestinal stem cells (research project)U01DK085525 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI WONG, MELISSA H. · 2009 to 2014
$2.0M
Genetic Control of Intestinal Epithelial Stem Cell Maintenance & DifferentiationR01DK091427 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MAGNESS, SCOTT T · 2011 to 2015
$1.6M
Beta-catenin's role in establishing the gut stem cell nicheR01DK068326 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI WONG, MELISSA H. · 2005 to 2009
$1.6M
NCI NIH HHS P30 CA033572NCI NIH HHS P30 CA069533NCI NIH HHS T32 CA106195NIDDK NIH HHS P30 DK034987NIDDK NIH HHS R01 DK091427NIDDK NIH HHS U01 DK085525NIDDK NIH HHS U01 DK085532NIDDK NIH HHS U24 DK085532
6 · The paper itself

Abstract

BACKGROUND &

aimsContinual renewal of the intestinal epithelium is dependent on active- and slow-cycling stem cells that are confined to the crypt base. Tight regulation of these stem cell populations maintains homeostasis by balancing proliferation and differentiation to support critical intestinal functions. The hierarchical relation of discrete stem cell populations in homeostasis or during regenerative epithelial repair remains controversial. Although recent studies have supported a model for the active-cycling leucine-rich repeat-containing G-protein-coupled receptor 5 (Lgr5)

methodsWe used novel monoclonal antibodies (mAbs) raised against murine intestinal epithelial cells in conjunction with ISC-green fluorescent protein (GFP) reporter mice to analyze relations between ISC populations by microscopy. Ex vivo 3-dimensional cultures, flow cytometry, and quantitative reverse-transcription polymerase chain reaction analyses were performed.

resultsTwo novel mAbs recognized distinct subpopulations of the intestinal epithelium and when used in combination permitted isolation of discrete Lgr5

conclusionsThese data showed the functional utility of murine mAbs in the isolation and investigation of Lgr5

Indexed as

3D, 3-dimensional4-OHT, 4-hydroxytamoxifenAPC, allophycocyaninBmi1Bmi1, B lymphoma Mo-MLV insertion region 1 homologcDNA, complementary DNAEgf, epidermal growth factorFACS, fluorescence-activated cell sortingGFP, green fluorescent proteinHBSS, Hank’s balanced salt solutionHierarchyIntestinal Stem CellsISC, intestinal stem cellLgr5Lgr5, leucine-rich repeat-containing G-protein–coupled receptor 5Lyz, lysozymemAb, monoclonal antibodymRNA, messenger RNAOHSU, Oregon Health and Science UniversityPBS, phosphate-buffered salinePE, PhycoerythrinPlasticityqRT-PCR, quantitative reverse-transcription polymerase chain reactionRspo1, R-spondin1TdT, tdTomatoWnt, wingless-type MMTV (mouse mammary tumor virus) integration site

Identifiers

PMID29928673
PMCPMC6008251
OpenAlexW2791242307

What OpenQuestion holds

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Registered trials

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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.