Evidence map›Paper›PMID 37419106›Full record

ArticleCell stem cell2023

Organ function is preserved despite reorganization of niche architecture in the hair follicle.

Haoyang Wei, Shuangshuang Du, Jeeun Parksong, H Amalia Pasolli, Catherine Matte-Martone, Sergi Regot, Lauren E Gonzalez, Tianchi Xin, Valentina Greco

Open access · greenAbstract read
In one paragraph

Article in Cell stem cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Matricellular Proteins in the Homeostasis, Regeneration, and Aging of Skin.International journal of molecular sciences · 2023
    Review
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

9 authors at 4 institutions in 1 country.

Haoyang WeiDepartment of Genetics, Yale School of Medicine, New Haven, CT 06510, USA.
Shuangshuang DuDepartment of Genetics, Yale School of Medicine, New Haven, CT 06510, USA.
Jeeun ParksongDepartments of Cell Biology and Pathology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
H Amalia PasolliElectron Microscopy Resource Center, The Rockefeller University, New York, NY 10065, USA.
Catherine Matte-MartoneDepartment of Genetics, Yale School of Medicine, New Haven, CT 06510, USA.
Sergi RegotDepartment of Molecular Biology and Genetics, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Lauren E GonzalezDepartment of Genetics, Yale School of Medicine, New Haven, CT 06510, USA.
Tianchi XinDepartment of Genetics, Yale School of Medicine, New Haven, CT 06510, USA. Electronic address: tianchi.xin@yale.edu.
Valentina GrecoDepartment of Genetics, Yale School of Medicine, New Haven, CT 06510, USA; Departments of Cell Biology and Dermatology, Yale Stem Cell Center, Yale Cancer Center, Yale School of Medicine, New Haven, CT 06510, USA. Electronic address: valentina.greco@yale.edu.
Yale University · USJohns Hopkins Medicine · USRockefeller University · USYale Cancer Center · US

Funding

Live Imaging of Skin RegenerationR01AR063663 · NIAMS · YALE UNIVERSITY · PI Valentina Greco · 2012 to 2026
$7.7M
Understanding Skin Tissue Repair in Live MammalsR01AR072668 · NIAMS · YALE UNIVERSITY · PI Valentina Greco · 2018 to 2026
$6.2M
Defining the role of mutational burden in sustaining normal homeostasis during agingDP1AG066590 · NIA · YALE UNIVERSITY · PI GRECO, VALENTINA · 2019 to 2023
$5.9M
Single Cell Analysis of MAPK Signaling Dynamics in MulticellularityR35GM133499 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Sergi Regot · 2019 to 2026
$3.3M
Normal stem cells and their transition to disease in the skinR01AR067755 · NIAMS · YALE UNIVERSITY · PI GRECO, VALENTINA · 2016 to 2020
$2.2M
NIAMS NIH HHS R01 AR063663NIAMS NIH HHS R01 AR067755NIAMS NIH HHS R01 AR072668NIA NIH HHS DP1 AG066590NIGMS NIH HHS R35 GM133499
6 · The paper itself

Abstract

The ability of stem cells to build and replenish tissues depends on support from their niche. Although niche architecture varies across organs, its functional importance is unclear. During hair follicle growth, multipotent epithelial progenitors build hair via crosstalk with their remodeling fibroblast niche, the dermal papilla, providing a powerful model to functionally interrogate niche architecture. Through mouse intravital imaging, we show that dermal papilla fibroblasts remodel individually and collectively to form a morphologically polarized, structurally robust niche. Asymmetric TGF-β signaling precedes morphological niche polarity, and loss of TGF-β signaling in dermal papilla fibroblasts leads them to progressively lose their stereotypic architecture, instead surrounding the epithelium. The reorganized niche induces the redistribution of multipotent progenitors but nevertheless supports their proliferation and differentiation. However, the differentiated lineages and hairs produced by progenitors are shorter. Overall, our results reveal that niche architecture optimizes organ efficiency but is not absolutely essential for organ function.

Indexed as

HairHair FollicleAnimalsCell DifferentiationEpitheliumMiceTransforming Growth Factor betaTransforming Growth Factor betahair follicleintravital imagingregenerationskin fibroblastsstem cell nichetissue architecture

Identifiers

PMID37419106
PMCPMC10362479
OpenAlexW4383312399

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.