Evidence map›Paper›PMID 38421110›Full record

ArticleCell proliferation2024

Functional analysis and transcriptome profile of meninges and skin fibroblasts from human-aged donors.

Valentina Fantini, Riccardo Rocco Ferrari, Matteo Bordoni, Eleonora Spampinato, Cecilia Pandini, Annalisa Davin, Valentina Medici, Stella Gagliardi, Antonio Guaita, Orietta Pansarasa and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

12 authors at 5 institutions in 3 countries.

Valentina FantiniLaboratory of Neurobiology and Neurogenetic, Golgi-Cenci Foundation, Abbiategrasso, Italy.ORCID https://orcid.org/0000-0003-1244-4453
Riccardo Rocco FerrariLaboratory of Neurobiology and Neurogenetic, Golgi-Cenci Foundation, Abbiategrasso, Italy.
Matteo BordoniCellular Model and Neuroepigenetics Unit, IRCCS Mondino Foundation, Pavia, Italy.ORCID https://orcid.org/0000-0001-9461-756X
Eleonora SpampinatoCellular Model and Neuroepigenetics Unit, IRCCS Mondino Foundation, Pavia, Italy.
Cecilia PandiniMolecular Biology and Transcriptomics Unit, IRCCS Mondino Foundation, Pavia, Italy.
Annalisa DavinLaboratory of Neurobiology and Neurogenetic, Golgi-Cenci Foundation, Abbiategrasso, Italy.
Valentina MediciDepartment of Neurology and Neuropathology, Golgi-Cenci Foundation, Abbiategrasso, Italy.
Stella GagliardiMolecular Biology and Transcriptomics Unit, IRCCS Mondino Foundation, Pavia, Italy.
Antonio GuaitaLaboratory of Neurobiology and Neurogenetic, Golgi-Cenci Foundation, Abbiategrasso, Italy.
Orietta PansarasaCellular Model and Neuroepigenetics Unit, IRCCS Mondino Foundation, Pavia, Italy.
Cristina CeredaCenter of Functional Genomics and Rare Diseases, Department of Pediatrics, Buzzi Children's Hospital, Milan, Italy.ORCID https://orcid.org/0000-0001-9571-0862
Tino Emanuele PoloniDepartment of Neurology and Neuropathology, Golgi-Cenci Foundation, Abbiategrasso, Italy.
Fondazione Golgi Cenci · ITFoundation Center · USOspedale dei Bambini Vittore Buzzi · ITUniversity of Milan · ITUniversity of Pavia · IT

Funding

Fondo di Beneficenza Intesa Sanpaolo B/2022/0094Ricerca Corrente 2022-2024, Italian Ministry of Health
6 · The paper itself

Abstract

The central nervous system (CNS) is surrounded by three membranes called meninges. Specialised fibroblasts, originating from the mesoderm and neural crest, primarily populate the meninges and serve as a binding agent. Our goal was to compare fibroblasts from meninges and skin obtained from the same human-aged donors, exploring their molecular and cellular characteristics related to CNS functions. We isolated meningeal fibroblasts (MFs) from brain donors and skin fibroblasts (SFs) from the same subjects. A functional analysis was performed measuring cell appearance, metabolic activity, and cellular orientation. We examined fibronectin, serpin H1, β-III-tubulin, and nestin through qPCR and immunofluorescence. A whole transcriptome analysis was also performed to characterise the gene expression of MFs and SFs. MFs appeared more rapidly in the post-tissue processing, while SFs showed an elevated cellular metabolism and a well-defined cellular orientation. The four markers were mostly similar between the MFs and SFs, except for nestin, more expressed in MFs. Transcriptome analysis reveals significant differences, particularly in cyclic adenosine monophosphate (cAMP) metabolism and response to forskolin, both of which are upregulated in MFs. This study highlights MFs' unique characteristics, including the timing of appearance, metabolic activity, and gene expression patterns, particularly in cAMP metabolism and response to forskolin. These findings contribute to a deeper understanding of non-neuronal cells' involvement in CNS activities and potentially open avenues for therapeutic exploration.

Indexed as

FibroblastsMeningesSkinTranscriptomeAgedCells, CulturedColforsinCyclic AMPFemaleGene Expression ProfilingHumansMaleMiddle AgedNestinColforsinCyclic AMPNestin

Identifiers

PMID38421110
PMCPMC11294439
OpenAlexW4392294636

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.