Evidence map›Paper›PMID 21081061›Full record

ArticleBiophysical journal2010

Spatial dynamics of multistage cell lineages in tissue stratification.

Ching-Shan Chou, Wing-Cheong Lo, Kimberly K Gokoffski, Yong-Tao Zhang, Frederic Y M Wan, Arthur D Lander, Anne L Calof, Qing Nie

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

26 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  10. STOCHASTIC DYNAMICS OF CELL LINEAGE IN TISSUE HOMEOSTASIS.Discrete and continuous dynamical systems. Series B · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Deciphering principles of morphogenesis from temporal and spatial patterns on the integument.Developmental dynamics : an official publication of the American Association of Anatomists · 2015
    Article
  15. Article
  16. Mathematical model of adult stem cell regeneration with cross-talk between genetic and epigenetic regulation.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  17. Article
  18. Article
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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

8 authors at 3 institutions in 1 country.

Ching-Shan ChouDepartment of Mathematics, The Ohio State University, Columbus, OH, USA. chou@math.ohio-state.edu
Wing-Cheong Lo
Kimberly K Gokoffski
Yong-Tao Zhang
Frederic Y M Wan
Arthur D Lander
Anne L Calof
Qing Nie
University of California, Irvine · USThe Ohio State University · USUniversity of Notre Dame · US

Funding

University of Iowa Clinical and Translational Science Program (TL1)UL1RR025755 · NCRR · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2008 to 2011
$26.3M
Uncover Strategies Used By Biological SystemsP50GM076516 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D · 2007 to 2016
$25.1M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM008620 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GOLDIN, ALAN L · 1999 to 2023
$8.1M
Principles of Robust Developmental PatterningR01GM067247 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D, NIE, QING · 2002 to 2014
$4.7M
TRAINING PROGRAM IN CELLULAR AND MOLECULAR NEUROSCIENCET32NS007444 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D · 1997 to 2007
$903k
NCRR NIH HHS UL1 RR025755NIDCD NIH HHS DC03580NIGMS NIH HHS GM08620NIGMS NIH HHS GM76516NIGMS NIH HHS P50 GM076516NIGMS NIH HHS R01 GM067247NIGMS NIH HHS T32 GM008620NINDS NIH HHS NS07444NINDS NIH HHS T32 NS007444
6 · The paper itself

Abstract

In developing and self-renewing tissues, terminally differentiated (TD) cell types are typically specified through the actions of multistage cell lineages. Such lineages commonly include a stem cell and multiple progenitor (transit-amplifying) cell stages, which ultimately give rise to TD cells. As the tissue reaches a tightly controlled steady-state size, cells at different lineage stages assume distinct spatial locations within the tissue. Although tissue stratification appears to be genetically specified, the underlying mechanisms that direct tissue lamination are not yet completely understood. Herein, we use modeling and simulations to explore several potential mechanisms that can be utilized to create stratification during developmental or regenerative growth in general systems and in the model system, the olfactory epithelium of mouse. Our results show that tissue stratification can be generated and maintained through controlling spatial distribution of diffusive signaling molecules that regulate the proliferation of each cell type within the lineage. The ability of feedback molecules to stratify a tissue is dependent on a low TD death rate: high death rates decrease tissue lamination. Regulation of the cell cycle lengths of stem cells by feedback signals can lead to transient accumulation of stem cells near the base and apex of tissue.

Indexed as

Models, BiologicalOrgan SpecificityAnimalsCell CountCell CycleCell DeathCell DifferentiationCell LineageCell Membrane PermeabilityCell PolarityDiffusionEpitheliumMiceStem Cell NicheStem CellsStromal Cells

Identifiers

PMID21081061
PMCPMC2980753
OpenAlexW2114351911

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.