Evidence map›Paper›PMID 31535975›Full record

ArticleeLife2019

A distinct transition from cell growth to physiological homeostasis in the tendon.

Mor Grinstein, Heather L Dingwall, Luke D O'Connor, Ken Zou, Terence Dante Capellini, Jenna Lauren Galloway

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 61 citations in OpenAlex.

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  14. A latent Axin2NPJ Regenerative medicine · 2024
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  15. Focal adhesion kinase regulates tendon cell mechanoresponse and physiological tendon development.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
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  17. Interfacial Tissue Regeneration with Bone.Current osteoporosis reports · 2024
    Review
  18. Article
  19. Article
  20. The regenerative capacity of neonatal tissues.Development (Cambridge, England) · 2022
    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

6 authors at 2 institutions in 1 country.

Mor GrinsteinCenter for Regenerative Medicine, Department of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, United States.ORCID 0000-0001-7166-5593
Heather L DingwallDepartment of Human Evolutionary Biology, Harvard University, Cambridge, United States.ORCID 0000-0003-2377-9777
Luke D O'ConnorCenter for Regenerative Medicine, Department of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, United States.
Ken ZouCenter for Regenerative Medicine, Department of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, United States.
Terence Dante CapelliniDepartment of Human Evolutionary Biology, Harvard University, Cambridge, United States.ORCID 0000-0003-3842-8478
Jenna Lauren GallowayCenter for Regenerative Medicine, Department of Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, United States.ORCID 0000-0003-3792-3290
Harvard University · USBroad Institute · US

Funding

Elucidating the function of a distinct cell population in adult mammalian tendonsR21AR072294 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI GALLOWAY, JENNA L · 2017 to 2018
$414k
Identifying gene and regulatory networks underlying postnatal tendon cell growthR21AR071554 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI CAPELLINI, TERENCE D, GALLOWAY, JENNA L · 2017 to 2018
$405k
NIAMS NIH HHS AR071554NIAMS NIH HHS AR072294NIAMS NIH HHS R21 AR071554NIAMS NIH HHS R21 AR072294
6 · The paper itself

Abstract

Changes in cell proliferation define transitions from tissue growth to physiological homeostasis. In tendons, a highly organized extracellular matrix undergoes significant postnatal expansion to drive growth, but once formed, it appears to undergo little turnover. However, tendon cell activity during growth and homeostatic maintenance is less well defined. Using complementary methods of genetic H2B-GFP pulse-chase labeling and BrdU incorporation in mice, we show significant postnatal tendon cell proliferation, correlating with longitudinal Achilles tendon growth. Around day 21, there is a transition in cell turnover with a significant decline in proliferation. After this time, we find low amounts of homeostatic tendon cell proliferation from 3 to 20 months. These results demonstrate that tendons harbor significant postnatal mitotic activity, and limited, but detectable activity in adult and aged stages. It also points towards the possibility that the adult tendon harbors resident tendon progenitor populations, which would have important therapeutic implications.

Indexed as

Achilles TendonAnimalsCell CycleCell ProliferationExtracellular MatrixHomeostasisMiceStem Cellsdevelopmental biologyhomeostasismousemusculoskeletalregenerative medicinestem cellstendontissue growth

Identifiers

PMID31535975
PMCPMC6791717
OpenAlexW2973299848

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.