Evidence map›Paper›PMID 39000224›Full record

ArticleInternational journal of molecular sciences2024

Characterization of Proteome Changes in Aged and Collagen VI-Deficient Human Pericyte Cultures.

Manuela Moriggi, Enrica Torretta, Matilde Cescon, Loris Russo, Ilaria Gregorio, Paola Braghetta, Patrizia Sabatelli, Cesare Faldini, Luciano Merlini, Cesare Gargioli and 3 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Manuela MoriggiDepartment of Biomedical Sciences for Health, University of Milano, 20133 Milano, Italy.ORCID 0000-0002-4718-0307
Enrica TorrettaLaboratory of Proteomics and Lipidomics, IRCCS Orthopedic Institute Galeazzi, 20161 Milano, Italy.ORCID 0000-0002-6374-3325
Matilde CesconDepartment of Molecular Medicine, University of Padova, 35121 Padova, Italy.ORCID 0000-0001-7138-1857
Loris RussoDepartment of Molecular Medicine, University of Padova, 35121 Padova, Italy.ORCID 0009-0002-6261-3593
Ilaria GregorioDepartment of Molecular Medicine, University of Padova, 35121 Padova, Italy.
Paola BraghettaDepartment of Molecular Medicine, University of Padova, 35121 Padova, Italy.ORCID 0000-0003-2547-8679
Patrizia SabatelliCNR-Institute of Molecular Genetics, 40136 Bologna, Italy.
Cesare Faldini1st Orthopedics and Traumatology Department, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy.
Luciano MerliniDepartment of Biomedical and Neuromotor Science, DIBINEM, University of Bologna, 40136 Bologna, Italy.ORCID 0000-0002-1108-1198
Cesare GargioliDepartment of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.ORCID 0000-0003-1742-3969
Paolo BonaldoDepartment of Molecular Medicine, University of Padova, 35121 Padova, Italy.
Cecilia GelfiDepartment of Biomedical Sciences for Health, University of Milano, 20133 Milano, Italy.ORCID 0000-0002-2996-6912
Daniele CapitanioDepartment of Biomedical Sciences for Health, University of Milano, 20133 Milano, Italy.ORCID 0000-0001-7701-728X

Funding

European Union - Next Generation EU Project CN00000041, CUP B93D21010860004Ministero dell'istruzione e del merito 201742SBXAMinistero dell'istruzione e del merito 2022MXH3JYtelethon foundation GGP19229
6 · The paper itself

Abstract

Pericytes are a distinct type of cells interacting with endothelial cells in blood vessels and contributing to endothelial barrier integrity. Furthermore, pericytes show mesenchymal stem cell properties. Muscle-derived pericytes can demonstrate both angiogenic and myogenic capabilities. It is well known that regenerative abilities and muscle stem cell potential decline during aging, leading to sarcopenia. Therefore, this study aimed to investigate the potential of pericytes in supporting muscle differentiation and angiogenesis in elderly individuals and in patients affected by Ullrich congenital muscular dystrophy or by Bethlem myopathy, two inherited conditions caused by mutations in collagen VI genes and sharing similarities with the progressive skeletal muscle changes observed during aging. The study characterized pericytes from different age groups and from individuals with collagen VI deficiency by mass spectrometry-based proteomic and bioinformatic analyses. The findings revealed that aged pericytes display metabolic changes comparable to those seen in aging skeletal muscle, as well as a decline in their stem potential, reduced protein synthesis, and alterations in focal adhesion and contractility, pointing to a decrease in their ability to form blood vessels. Strikingly, pericytes from young patients with collagen VI deficiency showed similar characteristics to aged pericytes, but were found to still handle oxidative stress effectively together with an enhanced angiogenic capacity.

Indexed as

Collagen Type VIPericytesProteomeAdultAgedAgingCell DifferentiationCells, CulturedFemaleHumansMaleMiddle AgedOxidative StressProteomicsCollagen Type VIProteomeBethlem myopathymuscle agingmyogenic differentiationpericyteskeletal muscleUllrich congenital muscular dystrophy

Identifiers

PMID39000224
PMCPMC11241165

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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 Socratic graph.