Evidence map›Paper›PMID 42282629›Full record

ArticlebioRxiv : the preprint server for biology2026

Hyaluronic Acid-Alginate Hydrazone Crosslinked Hydrogels Support the Generation and Maturation of V2a Interneurons.

Alycia N Galindo, Madison E McLaren, Alyssa K Chi, Jenna D Khachatourian, Jessica C Butts, Marian H Hettiaratchi

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Alycia N GalindoPhil and Penny Knight Campus for Accelerating Scientific Impact, University of Oregon, Eugene, OR.ORCID 0000-0002-3398-0506
Madison E McLarenDepartment of Bioengineering, Rice University, Houston, TX.
Alyssa K ChiPhil and Penny Knight Campus for Accelerating Scientific Impact, University of Oregon, Eugene, OR.
Jenna D KhachatourianPhil and Penny Knight Campus for Accelerating Scientific Impact, University of Oregon, Eugene, OR.ORCID 0009-0002-9972-6540
Jessica C ButtsDepartment of Bioengineering, Rice University, Houston, TX.
Marian H HettiaratchiPhil and Penny Knight Campus for Accelerating Scientific Impact, University of Oregon, Eugene, OR.ORCID 0000-0001-8187-4575

Funding

A Directed Evolution Approach to Affinity-Based Protein DeliveryR21EB032112 · NIBIB · UNIVERSITY OF OREGON · PI HETTIARATCHI, MARIAN HIRUSHIKA · 2021 to 2023
$602k
NIBIB NIH HHS R21 EB032112
6 · The paper itself

Abstract

Injury to the central nervous system (CNS) causes inflammation, cell death, and glial scar formation that inhibits tissue repair. Injectable hydrogels modified with extracellular matrix (ECM)-derived peptides can provide biochemical cues to promote neural tissue repair and serve as a vehicle to deliver therapeutics across the blood-spinal/blood-brain barrier in a minimally invasive manner. We developed an injectable hydrazone crosslinked hyaluronic acid-alginate (HA-Alg) hydrogel for neural tissue repair. We fabricated hydrogels with a range of polymer concentrations and evaluated their physicochemical properties to identify formulations that mimic the stiffness and viscoelastic properties of the CNS tissue environment. Hyaluronic acid was further modified with ECM-derived, cell-adhesive peptides (RGD and IKVAV) to enhance neuronal adhesion and viability. To evaluate the therapeutic potential of our hydrogel platform, we embedded mouse embryonic stem cell aggregates and differentiated them toward mature V2a interneurons. These interneurons are critical for relaying motor signals and represent a promising therapeutic cell population for treating spinal cord injuries. We demonstrated successful enrichment for V2a interneurons in HA-Alg hydrogels containing ECM-derived peptides. Interestingly, both our newly described HA-Alg and established crosslinked HA-HA hydrogels containing IKVAV peptides demonstrated significantly increased neurite length in interneuron enriched cultures compared to hydrogels without peptides. This study demonstrates that the addition of ECM-derived peptides is essential to support the neuronal adhesion and viability required for functional CNS tissue repair.

Identifiers

PMID42282629
PMCPMC13251969

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.