Evidence map›Paper›PMID 38878257›Full record

ArticleAngiogenesis2024

A C-type lectin from Bothrops jararacussu venom reprograms endothelial cell biology.

Federico G Baudou, Nancy L Charó, Marco A Scheidegger, Juan C Stupirski, Juan M Pérez Sáez, María F Troncoso, Mora Massaro, Adolfo R de Roodt, Mauricio C De Marzi, Mirta Schattner and 1 more

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Angiogenesis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

11 authors.

Federico G BaudouLaboratorio de Glicomedicina, Instituto de Biología y Medicina Experimental, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), C1428, Buenos Aires, Argentina.ORCID 0000-0003-1349-3820
Nancy L Charó *Laboratorio de Trombosis Experimental e Inmunobiología de la Inflamación, Instituto de Medicina Experimental (IMEX), CONICET-Academia Nacional de Medicina, C1425, Buenos Aires, Argentina.
Marco A Scheidegger *Laboratorio de Glicomedicina, Instituto de Biología y Medicina Experimental, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), C1428, Buenos Aires, Argentina.
Juan C StupirskiLaboratorio de Glicomedicina, Instituto de Biología y Medicina Experimental, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), C1428, Buenos Aires, Argentina.
Juan M Pérez SáezLaboratorio de Glicomedicina, Instituto de Biología y Medicina Experimental, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), C1428, Buenos Aires, Argentina.
María F TroncosoUniversidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Departamento de Química Biológica, C1113, Buenos Aires, Argentina.
Mora MassaroLaboratorio de Glicómica Funcional y Molecular, Instituto de Biología y Medicina Experimental, CONICET, C1428, Buenos Aires, Argentina.
Adolfo R de RoodtÁrea de Investigación y Desarrollo de Venenos, Instituto Nacional de Producción de Biológicos, Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbrán", Ministerio de Salud de la Nación, C1282, Buenos Aires, Argentina.
Mauricio C De MarziDepartamento de Ciencias Básicas, Universidad Nacional de Luján, C6700, Luján, Buenos Aires, Argentina.
Mirta SchattnerLaboratorio de Glicomedicina, Instituto de Biología y Medicina Experimental, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), C1428, Buenos Aires, Argentina.
Gabriel A RabinovichLaboratorio de Glicomedicina, Instituto de Biología y Medicina Experimental, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), C1428, Buenos Aires, Argentina. gabyrabi@gmail.com.ORCID 0000-0002-0947-8735

Funding

Agencia Nacional de Ciencia, Tecnología e Innovación PICT 2019-01109Agencia Nacional de Ciencia, Tecnología e Innovación PICT 2019-2307Agencia Nacional de Ciencia, Tecnología e Innovación PICT 2020-01552Universidad Nacional de Luján IeF 2022-005
6 · The paper itself

Abstract

Snake venoms are intricate mixtures of enzymes and bioactive factors that induce a range of detrimental effects in afflicted hosts. Certain Viperids, including Bothrops jararacussu, harbor C-type lectins (CTLs) known for their modulation of a variety of host cellular responses. In this study, we isolated and purified BjcuL, a CTL from B. jararacussu venom and investigated its impact on endothelial cell behavior, contrasting it with human galectin-1 (Gal-1), a prototype member of the galectin family with shared β-galactoside-binding activity. We found that BjcuL binds to human dermal microvascular endothelial cells (HMECs) in a concentration- and carbohydrate-dependent fashion and reprograms the function of these cells, favoring a pro-inflammatory and pro-coagulant endothelial phenotype. In light of the quest for universal antagonists capable of mitigating the harmful consequences of snake venoms, BjcuL emerges as a promising target to be blocked in order to regulate pathological endothelial cell responses.

Indexed as

BothropsCrotalid VenomsEndothelial CellsLectins, C-TypeAnimalsHumansVenomous SnakesBJcuL lectin, Bothrops jararacussuCrotalid VenomsLectins, C-TypeC-type lectinEndothelial cellsGalectin-1InflammationSnake venom

Identifiers

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.