Evidence map›Paper›PMID 36778338›Full record

ArticlebioRxiv : the preprint server for biology2023

Endogenous Tenocyte Activation Underlies the Regenerative Capacity of Adult Zebrafish Tendon.

Stephanie L Tsai, Steffany Villasenor, Rishita Shah, Jenna L Galloway

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Steffany Villasenor
Rishita Shah
Jenna L Galloway
Harvard University · USBarnard College · US

Funding

Mechanisms underlying tendon regeneration and attachment site pattern restorationR01AR074541 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI GALLOWAY, JENNA L · 2019 to 2023
$1.8M
Genetic and chemical screening in zebrafish to study tendon developmentR00HD069533 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI GALLOWAY, JENNA L · 2013 to 2015
$677k
The origin and function of tendon progenitors in craniofacial morphogenesis and patterningR03DE024771 · NIDCR · MASSACHUSETTS GENERAL HOSPITAL · PI GALLOWAY, JENNA L · 2015 to 2016
$261k
NIAMS NIH HHS R01 AR074541NICHD NIH HHS R00 HD069533NIDCR NIH HHS R03 DE024771
6 · The paper itself

Abstract

Tendons are essential, frequently injured connective tissues that transmit forces from muscle to bone. Their unique highly ordered, matrix-rich structure is critical for proper function. While adult mammalian tendons heal after acute injuries, endogenous tendon cells, or tenocytes, fail to respond appropriately, resulting in the formation of disorganized fibrovascular scar tissue with impaired function and increased propensity for re-injury. Here, we show that unlike mammals, adult zebrafish tenocytes activate upon injury and fully regenerate the tendon. Using a full tear injury model in the adult zebrafish craniofacial tendon, we defined the hallmark stages and cellular basis of tendon regeneration through multiphoton imaging, lineage tracing, and transmission electron microscopy approaches. Remarkably, we observe that the zebrafish tendon can regenerate and restore normal collagen matrix ultrastructure by 6 months post-injury (mpi). We show that tendon regeneration progresses in three main phases: inflammation within 24 hours post-injury (hpi), cellular proliferation and formation of a cellular bridge between the severed tendon ends at 3-5 days post-injury (dpi), and re-differentiation and matrix remodeling beginning from 5 dpi to 6 mpi. Importantly, we demonstrate that pre-existing tenocytes are the main cellular source of regeneration. Collectively, our work debuts the zebrafish tendon as one of the only reported adult tendon regenerative models and positions it as an invaluable comparative system to identify regenerative mechanisms that may inspire new tendon injury treatments in the clinic.

Identifiers

PMID36778338
PMCPMC9915736
OpenAlexW4319265351

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.