Evidence map›Paper›PMID 31907414›Full record

ArticleNature cell biology2020

Circadian control of the secretory pathway maintains collagen homeostasis.

Joan Chang, Richa Garva, Adam Pickard, Ching-Yan Chloé Yeung, Venkatesh Mallikarjun, Joe Swift, David F Holmes, Ben Calverley, Yinhui Lu, Antony Adamson and 5 more

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed, 1 pooled it
13.9field-weighted citation impact, top 1% 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

126 citing papers in PubMed, 1 synthesis or guideline pooled it, 197 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  8. Review
  9. Loss of type III collagen has limited effect on tendon healing in young adult mice.Matrix biology : journal of the International Society for Matrix Biology · 2026
    Article
  10. Review
  11. Sex Disparity in Systemic Sclerosis-Associated Pulmonary Fibrosis.International journal of molecular sciences · 2026
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  16. Review
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66 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 2 countries.

Joan Chang *Wellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Richa Garva *Wellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Adam Pickard *Wellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Ching-Yan Chloé Yeung *Wellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Venkatesh MallikarjunWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.ORCID http://orcid.org/0000-0002-0284-5205
Joe SwiftWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.ORCID http://orcid.org/0000-0002-5039-9094
David F HolmesWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Ben CalverleyWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Yinhui LuWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Antony AdamsonWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.ORCID http://orcid.org/0000-0002-5408-0013
Helena Raymond-HaylingWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Oliver JensenSchool of Mathematics, Faculty of Science and Engineering, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0003-0172-6578
Tom ShearerSchool of Mathematics, Faculty of Science and Engineering, University of Manchester, Manchester, UK.
Qing Jun MengWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK. qing-jun.meng@manchester.ac.uk.ORCID http://orcid.org/0000-0002-9426-8336
Karl E KadlerWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK. karl.kadler@manchester.ac.uk.ORCID http://orcid.org/0000-0003-4977-4683
Manchester Academic Health Science Centre · GBUniversity of Manchester · GB

Funding

Arthritis Research UK 20875Medical Research Council MR/P010709/1RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/L024551/1Versus Arthritis 20875Wellcome Trust 110126Wellcome Trust 110126/Z/15/ZWellcome Trust 203128Wellcome Trust (Wellcome) 110126/Z/15/ZWellcome Trust (Wellcome) 203128/Z/16/ZWellcome Trust (Wellcome) 210062/Z/17/Z
6 · The paper itself

Abstract

Collagen is the most abundant secreted protein in vertebrates and persists throughout life without renewal. The permanency of collagen networks contrasts with both the continued synthesis of collagen throughout adulthood and the conventional transcriptional/translational homeostatic mechanisms that replace damaged proteins with new copies. Here, we show circadian clock regulation of endoplasmic reticulum-to-plasma membrane procollagen transport by the sequential rhythmic expression of SEC61, TANGO1, PDE4D and VPS33B. The result is nocturnal procollagen synthesis and daytime collagen fibril assembly in mice. Rhythmic collagen degradation by CTSK maintains collagen homeostasis. This circadian cycle of collagen synthesis and degradation affects a pool of newly synthesized collagen, while maintaining the persistent collagen network. Disabling the circadian clock causes abnormal collagen fibrils and collagen accumulation, which are reduced in vitro by the NR1D1 and CRY1/2 agonists SR9009 and KL001, respectively. In conclusion, our study has identified a circadian clock mechanism of protein homeostasis wherein a sacrificial pool of collagen maintains tissue function.

Indexed as

AnimalsAryl Hydrocarbon Receptor Nuclear TranslocatorCarbazolesCircadian ClocksCollagenCyclic Nucleotide Phosphodiesterases, Type 4Extracellular MatrixHomeostasisMice, TransgenicPyrrolidinesSecretory PathwaySEC Translocation ChannelsSulfonamidesThiophenesVesicular Transport ProteinsAryl Hydrocarbon Receptor Nuclear TranslocatorCarbazolesCollagenCyclic Nucleotide Phosphodiesterases, Type 4KL001PDE4D protein, mousePyrrolidinesSEC Translocation ChannelsSR9009SulfonamidesTANGO protein, mouseThiophenesVesicular Transport ProteinsVPS33B protein, mouse

Identifiers

PMID31907414
PMCPMC7613259
OpenAlexW2997202359

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.