Evidence map›Paper›PMID 31705125›Full record

ArticleNature protocols2019

Decellularization and antibody staining of mouse tissues to map native extracellular matrix structures in 3D.

Alejandro E Mayorca-Guiliani, Oliver Willacy, Chris D Madsen, Maria Rafaeva, Stefanie Elisabeth Heumüller, Felix Bock, Gerhard Sengle, Manuel Koch, Thomas Imhof, Frank Zaucke and 4 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature protocols, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
9.1field-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

44 citing papers in PubMed, 75 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 4 countries.

Alejandro E Mayorca-Guiliani *Biotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark. alejandro.mayorca@bric.ku.dk.ORCID http://orcid.org/0000-0001-8137-4722
Oliver Willacy *Biotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-1541-7795
Chris D MadsenDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0001-6838-2103
Maria RafaevaBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-7317-4058
Stefanie Elisabeth HeumüllerCenter for Biochemistry, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Felix BockDepartment of Ophthalmology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Gerhard SengleCenter for Biochemistry, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Manuel KochCenter for Biochemistry, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0002-2962-7814
Thomas ImhofCenter for Biochemistry, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Frank ZauckeDr. Rolf M. Schwiete Research Unit for Osteoarthritis, Orthopedic University Hospital Friedrichsheim gGmbH, Frankfurt, Germany.ORCID http://orcid.org/0000-0002-7680-9354
Raimund WagenerCenter for Biochemistry, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Takako SasakiDepartment of Biochemistry II, Faculty of Medicine, Oita University, Oita, Japan.
Janine T ErlerBiotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark. janine.erler@bric.ku.dk.ORCID http://orcid.org/0000-0001-8675-6527
Raphael Reuten *Biotech Research and Innovation Centre (BRIC), University of Copenhagen (UCPH), Copenhagen, Denmark. raphael.reuten@bric.ku.dk.ORCID http://orcid.org/0000-0002-9434-4108
University of Cologne · DEUniversity of Copenhagen · DKLund University · SEOita University · JPOrthopaedic University Hospital Friedrichsheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extracellular matrix (ECM) is a major regulator of homeostasis and disease, yet the 3D structure of the ECM remains poorly understood because of limitations in ECM visualization. We recently developed an ECM-specialized method termed in situ decellularization of tissues (ISDoT) to isolate native 3D ECM scaffolds from whole organs in which ECM structure and composition are preserved. Here, we present detailed surgical instructions to facilitate decellularization of 33 different mouse tissues and details of validated antibodies that enable the visualization of 35 mouse ECM proteins. Through mapping of these ECM proteins, the structure of the ECM can be determined and tissue structures visualized in detail. In this study, perfusion decellularization is presented for bones, skeletal muscle, tongue, salivary glands, stomach, duodenum, jejunum/ileum, large intestines, mesentery, liver, gallbladder, pancreas, trachea, bronchi, lungs, kidneys, urinary bladder, ovaries, uterine horn, cervix, adrenal gland, heart, arteries, veins, capillaries, lymph nodes, spleen, peripheral nerves, eye, outer ear, mammary glands, skin, and subcutaneous tissue. Decellularization, immunostaining, and imaging take 4-5 d.

Indexed as

AnimalsAntibodiesExtracellular MatrixImaging, Three-DimensionalMiceMice, Inbred BALB CMice, Inbred C57BLOrgan SpecificityPerfusionStaining and LabelingTissue EngineeringTissue ScaffoldsAntibodies

Identifiers

PMID31705125
OpenAlexW2983262330

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.