Evidence map›Paper›PMID 26691820›Full record

ArticleStem cell research2016

Cells with surface expression of CD133highCD71low are enriched for tripotent colony-forming progenitor cells in the adult murine pancreas.

Liang Jin, Dan Gao, Tao Feng, Jacob R Tremblay, Nadiah Ghazalli, Angela Luo, Jeffrey Rawson, Janine C Quijano, Jing Chai, Lena Wedeken and 8 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  8. Towards organoid culture without Matrigel.Communications biology · 2021
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  15. Single-cell resolution analysis of the human pancreatic ductal progenitor cell niche.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. Review
  17. Review
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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

18 authors at 3 institutions in 2 countries.

Liang JinDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States; State Key Laboratory of Natural Medicines, Biopharmaceutical College, China Pharmaceutical University, Tongjia Xiang 24, Nanjing, 210009, People's Republic of China.
Dan GaoDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Tao FengDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Jacob R TremblayDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Irell & Manella Graduate School of Biological Sciences, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Nadiah GhazalliDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Irell & Manella Graduate School of Biological Sciences, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Angela LuoDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Jeffrey RawsonDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Janine C QuijanoDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Jing ChaiDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Lena WedekenDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Jasper HsuDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Jeanne LeBonDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Stephanie WalkerDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Hung-Ping ShihDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Irell & Manella Graduate School of Biological Sciences, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
Alborz MahdaviDepartment of Bioengineering, California Institute of Technology, Pasadena, CA 91125, United States.
David A TirrellDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, United States.
Arthur D RiggsDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Irell & Manella Graduate School of Biological Sciences, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States.
H Teresa KuDepartment of Translational Research and Cellular Therapeutics, Diabetes and Metabolism Research Institute, Duarte, CA 91010, United States; Irell & Manella Graduate School of Biological Sciences, Duarte, CA 91010, United States; Beckman Research Institute of City of Hope, Duarte, CA 91010, United States. Electronic address: hku@coh.org.
Beckman Research InstituteCity of Hope · USCalifornia Institute of Technology · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI XIWEI WU · 1985 to 2026
$86.3M
EX VIVO DIFFERENTIATION AND EXPANSION OF ADULT PANCREATIC COLONY-FORMING UNITSR01DK099734 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI KU, HSUN TERESA · 2014 to 2018
$1.9M
Insulin-Expressing Colony Forming ProgenitorsR01DK081587 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI KU, HSUN TERESA · 2008 to 2012
$1.7M
Epitenetic regulation and enhancement of beta cell differentiationU01DK089533 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI RIGGS, ARTHUR D · 2010 to 2011
$1.0M
Fractionation, Purification and Characterization of Adult Pancreatic Colony-Forming Progenitor CellsR56DK099734 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI KU, HSUN TERESA · 2019 to 2019
$132k
NCI NIH HHS P30CA33572NIDDK NIH HHS R01 DK081587NIDDK NIH HHS R01DK081587NIDDK NIH HHS R01 DK099734NIDDK NIH HHS R01DK099734NIDDK NIH HHS R56 DK099734NIDDK NIH HHS U01 DK089533NIDDK NIH HHS U01DK089533
6 · The paper itself

Abstract

Progenitor cells in the adult pancreas are potential sources of endocrine beta cells for treating type 1 diabetes. Previously, we identified tri-potent progenitor cells in the adult (2-4month-old) murine pancreas that were capable of self-renewal and differentiation into duct, acinar, and endocrine cells in vitro. These progenitor cells were named pancreatic colony-forming units (PCFUs). However, because PCFUs are a minor population in the pancreas (~1%) they are difficult to study. To enrich PCFUs, strategies using cell-surface marker analyses and fluorescence-activated cell sorting were developed. We found that CD133(high)CD71(low) cells, but not other cell populations, enriched PCFUs by up to 30 fold compared to the unsorted cells. CD133(high)CD71(low) cells generated primary, secondary, and subsequent colonies when serially re-plated in Matrigel-containing cultures, suggesting self-renewal abilities. In the presence of a laminin hydrogel, CD133(high)CD71(low) cells gave rise to colonies that contained duct, acinar, and Insulin(+)Glucagon(+) double-hormonal endocrine cells. Colonies from the laminin hydrogel culture were implanted into diabetic mice, and five weeks later duct, acinar, and Insulin(+)Glucagon(-) cells were detected in the grafts, demonstrating tri-lineage differentiation potential of CD133(high)CD71(low) cells. These CD133(high)CD71(low) cells will enable future studies of putative adult pancreas stem cells in vivo.

Indexed as

AC133 AntigenColony-Forming Units AssayAcinar CellsAgingAnimalsAntigens, CDCell MembraneCell Self RenewalGlucagonImmunohistochemistryInsulinMice, Inbred C57BLMultipotent Stem CellsPancreasPancreatic DuctsParaffin EmbeddingAC133 AntigenAntigens, CDCD71 antigenGlucagonInsulinReceptors, TransferrinDifferentiationFluorescence-activated cell sorting (FACS)Heterogeneity of ductal cellsPancreatic colony-forming unitsSelf-renewal

Identifiers

PMID26691820
PMCPMC4762724
OpenAlexW2186222783

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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.