Evidence map›Paper›PMID 32360152›Full record

ArticleBiochimica et biophysica acta. General subjects2020

Matrix vesicle biomimetics harboring Annexin A5 and alkaline phosphatase bind to the native collagen matrix produced by mineralizing vascular smooth muscle cells.

Maytê Bolean, Benedetta Izzi, Soetkin van Kerckhoven, Massimo Bottini, Ana Paula Ramos, José Luis Millán, Marc F Hoylaerts, Pietro Ciancaglini

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta. General subjects, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 37 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

8 authors at 6 institutions in 4 countries.

Maytê BoleanDepartment of Chemistry, FFCLRP-USP, University of São Paulo, Ribeirão Preto, SP, Brazil.
Benedetta IzziDepartment of Epidemiology and Prevention, IRCCS NEUROMED, Pozzilli, IS, Italy.
Soetkin van KerckhovenFunctiemetingen Pneumologie, UZ Leuven Gasthuisberg, Leuven, Belgium.
Massimo BottiniUniversity of Rome Tor Vergata, Department of Experimental Medicine and Surgery, Roma, Italy; Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Ana Paula RamosDepartment of Chemistry, FFCLRP-USP, University of São Paulo, Ribeirão Preto, SP, Brazil.
José Luis MillánSanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Marc F HoylaertsCenter for Molecular and Vascular Biology, Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.
Pietro CiancagliniDepartment of Chemistry, FFCLRP-USP, University of São Paulo, Ribeirão Preto, SP, Brazil. Electronic address: pietro@ffclrp.usp.br.
Universidade de São Paulo · BRIstituto Neurologico Mediterraneo · ITKU Leuven · BESanford Burnham Prebys Medical Discovery Institute · USUniversitair Ziekenhuis Leuven · BEUniversity of Rome Tor Vergata · IT

Funding

MOLECULAR PATHOGENESIS/TREATMENT OF HYPOPHOSPHATASIAR01DE012889 · NIDCR · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MILLAN, JOSE LUIS · 1999 to 2020
$9.2M
NIDCR NIH HHS R01 DE012889
6 · The paper itself

Abstract

backgoundVascular smooth muscle cells (VSMCs) transdifferentiated ectopically trigger vascular calcifications, contributing to clinical cardiovascular disease in the aging population. AnxA5 and TNAP play a crucial role in (patho)physiological mineralization.

methodsWe performed affinity studies between DPPC and 9:1 DPPC:DPPS-proteoliposomes carrying AnxA5 and/or TNAP and different types of collagen matrix: type I, II, I + III and native collagenous extracellular matrix (ECM) produced from VSMCs with or without differentiation, to simulate ectopic calcification conditions.

resultsAnxA5-proteoliposomes had the highest affinity for collagens, specially for type II. TNAP-proteoliposomes bound poorly and the simultaneous presence of TNAP in the AnxA5-proteoliposomes disturbed interactions between AnxA5 and collagen. DPPC AnxA5-proteoliposomes affinities for ECM from transdifferentiating cells went up 2-fold compared to that from native VSMCs. The affinities of DPPC:DPPS-proteoliposomes were high for ECM from VSMCs with or without differentiation, underscoring a synergistic effect between AnxA5 and DPPS. Co-localization studies uncovered binding of proteoliposomes harboring AnxA5 or TNAP+AnxA5 to various regions of the ECM, not limited to type II collagen.

conclusionAnxA5-proteoliposomes showed the highest affinities for type II collagen, deposited during chondrocyte mineralization in joint cartilage. TNAP in the lipid/protein microenvironment disturbs interactions between AnxA5 and collagen. These findings support the hypothesis that TNAP is cleaved from the MVs membrane just before ECM binding, such facilitating MV anchoring to ECM via AnxA5 interaction. GENERAL SIGNIFICANCE: Proteoliposomes as MV biomimetics are useful in the understanding of mechanisms that regulate the mineralization process and may be essential for the development of novel therapeutic strategies to prevent or inhibit ectopic mineralization.

Indexed as

Alkaline PhosphataseAnnexin A5Binding SitesBiomimetic MaterialsCarrier ProteinsCell DifferentiationCollagenExtracellular MatrixHumansMuscle, Smooth, VascularProteolipidsAlkaline PhosphataseALPL protein, humanAnnexin A5ANXA5 protein, humanCarrier ProteinsCollagenProteolipidsproteoliposomesAlkaline phosphataseAnnexin A5CollagenMatrix vesiclesPhosphatidylserineProteoliposomes

Identifiers

PMID32360152
PMCPMC8370721
OpenAlexW3021855531

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.