Evidence map›Paper›PMID 39438030›Full record

ArticleImmunology and cell biology2025

Characterization of cellular and molecular immune components of the painted white sea urchin Lytechinus pictus in response to bacterial infection.

Katherine T Nesbit, Alexis Cody Hargadon, Gloria D Renaudin, Nicholas D Kraieski, Katherine M Buckley, Emily Darin, Yoon Lee, Amro Hamdoun, Catherine S Schrankel

Abstract read
In one paragraph

Article in Immunology and cell biology, 2025. 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. Cryopreservation of sea urchin (Lytechinus pictus) embryos and development through metamorphosis.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
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

9 authors.

Katherine T NesbitDepartment of Biology, San Diego State University, San Diego, CA, USA.ORCID 0000-0003-3437-7511
Alexis Cody HargadonScripps Institution of Oceanography, University of California San Diego, San Diego, CA, USA.
Gloria D RenaudinScripps Institution of Oceanography, University of California San Diego, San Diego, CA, USA.
Nicholas D KraieskiDepartment of Biological Sciences, Auburn University, Auburn, AL, USA.
Katherine M BuckleyDepartment of Biological Sciences, Auburn University, Auburn, AL, USA.ORCID 0000-0002-6585-8943
Emily DarinDepartment of Biology, San Diego State University, San Diego, CA, USA.
Yoon LeeScripps Institution of Oceanography, University of California San Diego, San Diego, CA, USA.
Amro HamdounScripps Institution of Oceanography, University of California San Diego, San Diego, CA, USA.
Catherine S SchrankelDepartment of Biology, San Diego State University, San Diego, CA, USA.

Funding

Identity, mechanisms and early life impacts of transporter interfering compoundsR01ES027921 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHANG, GEOFFREY A, HAMDOUN, AMRO M · 2018 to 2022
$3.0M
NIEHS NIH HHS ES027921NIEHS NIH HHS R01 ES027921
6 · The paper itself

Abstract

Sea urchins are basal deuterostomes that share key molecular components of innate immunity with vertebrates. They are a powerful model for the study of innate immune system evolution and function, especially during early development. Here we characterize the morphology and associated molecular markers of larval immune cell types in a newly developed model sea urchin, Lytechinus pictus. We then challenge larvae through infection with an established pathogenic Vibrio and characterize phenotypic and molecular responses. We contrast these to the previously described immune responses of the purple sea urchin Strongylocentrotus purpuratus. The results revealed shared cellular morphologies and homologs of known pigment cell immunocyte markers (PKS, srcr142) but a striking absence of subsets of perforin-like macpf genes in blastocoelar cell immunocytes. We also identified novel patterning of cells expressing a scavenger receptor cysteine rich (SRCR) gene in the coelomic pouches of the larva (the embryonic stem cell niche). The SRCR signal becomes further enriched in both pouches in response to bacterial infection. Collectively, these results provide a foundation for the study of immune responses in L. pictus. The characterization of the larval immune system of this rapidly developing and genetically enabled sea urchin species will facilitate more sophisticated studies of innate immunity and the crosstalk between the immune system and development.

Indexed as

Immunity, InnateAnimalsBacterial InfectionsImmunity, CellularLarvaLytechinusVibrioVibrio InfectionsBacterial infectioninnate immunitysea urchinSRCRstem cell

Identifiers

PMID39438030
PMCPMC11688612

What OpenQuestion holds

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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 OpenQuestion graph.