Evidence map›Paper›PMID 39953556›Full record

ArticleEvoDevo2025

A morphological cell atlas of the freshwater sponge Ephydatia muelleri with key insights from targeted single-cell transcriptomes.

Sally P Leys, Lauren Grombacher, Daniel Field, Glen R D Elliott, Vanessa R Ho, Amanda S Kahn, Pamela J Reid, Ana Riesgo, Emilio Lanna, Yuriy Bobkov and 2 more

Abstract read
In one paragraph

Article in EvoDevo, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Rethinking Plasticity in Sponges.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2026
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Why Homoscleromorph Sponges Have Ciliated Epithelia: Evidence for an Ancestral Role in Mucociliary Driven Particle Flux.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2025
    Article
  7. Article
  8. Sponge bHLH Gene Expression inInternational journal of molecular sciences · 2025
    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

12 authors.

Sally P LeysDepartment of Biological Sciences, University of Alberta, Edmonton, AB, T6G 2R3, Canada. sleys@ualberta.ca.
Lauren GrombacherDepartment of Biological Sciences, University of Alberta, Edmonton, AB, T6G 2R3, Canada.
Daniel FieldDepartment of Biological Sciences, University of Alberta, Edmonton, AB, T6G 2R3, Canada.
Glen R D ElliottDepartment of Biological Sciences, University of Alberta, Edmonton, AB, T6G 2R3, Canada.
Vanessa R HoDepartment of Biological Sciences, University of Alberta, Edmonton, AB, T6G 2R3, Canada.
Amanda S KahnDepartment of Biological Sciences, University of Alberta, Edmonton, AB, T6G 2R3, Canada.
Pamela J ReidDepartment of Biological Sciences, University of Alberta, Edmonton, AB, T6G 2R3, Canada.
Ana RiesgoDepartment of Biological Sciences, University of Alberta, Edmonton, AB, T6G 2R3, Canada.
Emilio LannaDepartment of Biological Sciences, University of Alberta, Edmonton, AB, T6G 2R3, Canada.
Yuriy BobkovWhitney Laboratory for Marine Bioscience, University of Florida, St. Augustine, FL, 32080, USA.
Joseph F RyanWhitney Laboratory for Marine Bioscience, University of Florida, St. Augustine, FL, 32080, USA.
April L HortonBiology Department, Bates College, Lewiston, MA, USA.

Funding

Gordon and Betty Moore Foundation 9332Natural Sciences and Engineering Research Council of Canada 2022-0314
6 · The paper itself

Abstract

How animal cell types, tissues, and regional body plans arose is a fundamental question in EvoDevo. Many current efforts attempt to link genetic information to the morphology of cells, tissues and regionalization of animal body plans using single-cell sequencing of cell populations. However, a lack of in-depth understanding of the morphology of non-bilaterian animals remains a considerable block to understanding the transitions between bilaterian and non-bilaterian cells and tissues. Sponges (Porifera), one of the earliest diverging animal phyla, pose a particular challenge to this endeavour, because their body plans lack mouths, gut, conventional muscle and nervous systems. With a goal to help bridge this gap, we have studied the morphology, behaviour and transcriptomics of cells and tissue types of an easily accessible and well-studied species of freshwater sponge, Ephydatia muelleri. New features described here include: a polarized external epithelium, a new contractile sieve cell that forms the entry to incurrent canals, motile cilia on apopyle cells at the exit of choanocyte chambers, and non-motile cilia on cells in excurrent canals and oscula. Imaging cells in vivo shows distinct behavioural characteristics of motile cells in the mesohyl. Transcriptomic phenotypes of three cell types (cystencytes, choanocytes and archaeocytes) captured live indicate that cell-type transcriptomes are distinct. Importantly, individual archaeocytes show a range of transcriptomic phenotypes which is supported by the distinct expression of different genes by subsets of this cell type. In contrast, all five choanocyte cells sampled live revealed highly uniform transcriptomes with significantly fewer genes expressed than in other cell types. Our study shows that sponges have tissues whose morphology and cell diversity are both functionally complex, but which together enable the sponge, like other metazoans, to sense and respond to stimuli.

Identifiers

PMID39953556
PMCPMC11827373

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.