Evidence map›Paper›PMID 39367491›Full record

ArticleNeural development2024

Terminal differentiation precedes functional circuit integration in the peduncle neurons in regenerating Hydra vulgaris.

Alondra Escobar, Soonyoung Kim, Abby S Primack, Guillaume Duret, Celina E Juliano, Jacob T Robinson

Abstract read
In one paragraph

Article in Neural development, 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. Article
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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

6 authors.

Alondra Escobar *Department of Bioengineering, Rice University, 6100 Main Street, Houston, TX, 77005, USA.
Soonyoung Kim *Department of Electrical and Computer Engineering, Rice University, 6100 Main Street, Houston, TX, 77005, USA.
Abby S PrimackDepartment of Molecular and Cellular Biology, University of California, Davis, CA, 95616, USA.
Guillaume DuretDepartment of Electrical and Computer Engineering, Rice University, 6100 Main Street, Houston, TX, 77005, USA.
Celina E JulianoDepartment of Molecular and Cellular Biology, University of California, Davis, CA, 95616, USA.
Jacob T RobinsonDepartment of Bioengineering, Rice University, 6100 Main Street, Houston, TX, 77005, USA. jtrobinson@rice.edu.

Funding

Mechanisms of Hydra Development and RegenerationR35GM133689 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Celina Juliano · 2019 to 2026
$3.3M
Developing microfluidics and automated image analysis for high-throughput investigation of lifespan and health in a novel invertebrate model for agingR21AG067034 · NIA · MARINE BIOLOGICAL LABORATORY · PI GRIBBLE, KRISTIN, ROBINSON, JACOB T. · 2020 to 2021
$456k
National Science Foundation IOS-1829158NIA NIH HHS R21 AG067034NIGMS NIH HHS R35 GM133689NIH HHS R21 AG067034NIH HHS R35 GM133689
6 · The paper itself

Abstract

Understanding how neural circuits are regenerated following injury is a fundamental question in neuroscience. Hydra is a powerful model for studying this process because it has a simple neural circuit structure, significant and reproducible regenerative abilities, and established methods for creating transgenics with cell-type-specific expression. While Hydra is a long-standing model for regeneration and development, little is known about how neural activity and behavior is restored following significant injury. In this study, we ask if regenerating neurons terminally differentiate prior to reforming functional neural circuits, or if neural circuits regenerate first and then guide the constituent naive cells toward their terminal fate. To address this question, we developed a dual-expression transgenic Hydra line that expresses a cell-type-specific red fluorescent protein (tdTomato) in ec5 peduncle neurons, and a calcium indicator (GCaMP7s) in all neurons. With this transgenic line, we can simultaneously record neural activity and track the reappearance of the terminally-differentiated ec5 neurons. Using SCAPE (Swept Confocally Aligned Planar Excitation) microscopy, we monitored both calcium activity and expression of tdTomato-positive neurons in 3D with single-cell resolution during regeneration of Hydra's aboral end. The synchronized neural activity associated with a regenerated neural circuit was observed approximately 4 to 8 hours after expression of tdTomato in ec5 neurons. These data suggest that regenerating ec5 neurons undergo terminal differentiation prior to re-establishing their functional role in the nervous system. The combination of dynamic imaging of neural activity and gene expression during regeneration make Hydra a powerful model system for understanding the key molecular and functional processes involved in neural regeneration following injury.

Indexed as

Animals, Genetically ModifiedCell DifferentiationHydraNerve RegenerationNeuronsAnimalsNerve NetRegenerationCell differentiationCnidariansFunctional neural circuitHydraNeural regenerationNeurogenesis

Identifiers

PMID39367491
PMCPMC11452936

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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.