Evidence mapPaperPMID 40378115Full record

ArticlePloS one2025

The neuronal chaperone proSAAS is highly expressed in the retina.

Nicholas Schaffer, Samira Mitias, Yan Guo, Steven L Bernstein, Iris Lindberg

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Nicholas SchafferDepartment of Neurobiology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0009-0001-7334-5451
Samira MitiasDepartment of Neurobiology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Yan GuoDepartment of Ophthalmology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Steven L BernsteinDepartment of Ophthalmology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0000-0001-7758-0136
Iris LindbergDepartment of Neurobiology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0000-0002-1188-170X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The many layers of the neuroretina contain a complex, interconnected network of specialized neurons that both process visual stimuli and conduct processed information to higher brain areas. Neural networks rely on proteostatic control mechanisms to maintain proper protein homeostasis both in cell bodies as well as within synapses; protein chaperones play an important role in regulating and supporting this process. ProSAAS is a small neuronal chaperone that functions as an anti-aggregant in in vitro assays and is released upon depolarization in neuronal primary cultures. We here report a potential role for proSAAS in the retina. A review of human and mouse retinal RNAseq studies reveals that proSAAS expression is abundant within the retina. Single cell sequencing data from mouse and human studies show that proSAAS levels are highest in retinal ganglion cells (RGCs) and horizontal cells. Using proSAAS antibodies in combination with antisera to known retinal cell markers in mouse retinal sections, we confirm RNAseq data showing that proSAAS expression is highest in RGCs and horizontal cells. The proSAAS signal is concentrated within the ganglion cell layer and the inner plexiform layer, a dense synaptic layer connecting retinal neurons. Western blotting of mouse retinal extracts indicates the presence of two processed proSAAS forms, a 21 kDa C-terminally processed form, and a small 13 kDa species which, based on antibody specificity, likely represents an internal fragment. This fragment is also found in extracts prepared from human retinas. Taken together, our data provide support for the hypothesis that retinal synapses utilize the proSAAS chaperone to support visual signaling.

Indexed as

Molecular ChaperonesRetinaAnimalsHumansMiceMice, Inbred C57BLRetinal Ganglion CellsMolecular Chaperones

Identifiers

PMID40378115
PMCPMC12083831

What Socratic 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 Socratic graph.