Data from: Time-dependent adaptations of damaged neurons and their microenvironment in the regenerating adult zebrafish spinal cord
Data files
Jan 22, 2026 version files 132.62 KB
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Dataset.xlsx
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README.md
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Abstract
Dataset DOI: 10.5061/dryad.bnzs7h4qj
Description of the data and file structure
File name: Dataset.xlsx
The dataset contains all the data used to generate the statistical analyses (as presented in Table S1) and figure panels (in both main figures and supplementary figures) included in this manuscript. In detail:
Figure 1
Panel B: Soma sizes of different neuronal populations, such as all Motoneurons (MNs), primary Motoneurons (pMNs), all V2a Interneurons (V2a-INs), dorsal V2a Interneurons (dV2a-INs).
Panel D: Number of dendritic intersections for different distances from the soma for both pMNs and dV2a-INs
Panel G: Maximum rostral projection of the dendrites of the uninjured and injured pMNs.
Panel H: Maximum rostral projection of the dendrites of the uninjured and injured dV2a-INs.
Panel I: Soma sizes of the pMNs and dV2-INs in uninjured (control) and injured (7 days post injury; dpi) animals.
Figure 2
Panel B: Number of c-Fos positive neurons in uninjured (control) and injured (3 dpi) animals.
Panel C: Proportion of c-Fos positive pMNs and dV2a-INs in uninjured (control) and injured (3 dpi) animals.
Panel G: Adaptation Index for uninjured (control) and injured (3 dpi, 7 dpi, and 14 dpi) pMNs and dV2a-INs.
Figure 3
Panel A: Mean EPSP frequency and EPSP amplitude obtained from uninjured (control) and injured (3 dpi, 7 dpi, and 14 dpi) pMNs.
Panel B: Mean EPSP frequency and EPSP amplitude obtained from uninjured (control) and injured (3 dpi, 7 dpi, and 14 dpi) dV2a-INs.
Panel C: Mean EPSP frequency, mean EPSP amplitude, and resting membrane potential (RMP) obtained from injured (3dpi) pMNs in control (Saline) and after application of NBQX and APV.
Panel D: Mean EPSP frequency, mean EPSP amplitude, and RMP obtained from injured (3dpi) dV2a-INs in control (Saline) and after application of NBQX and APV.
Panel F: Proportion of the SV2 positive sites that are GFP positive (V2a-IN positive).
Panel G: Number of perisomatic SV2-positive sites in uninjured (control) and injured (3 dpi, 7 dpi, and 14 dpi) pMNs.
Figure 4
Panel D: Normalized intensity of WFA staining in uninjured (control) and injured (3 dpi, 7 dpi and 14 dpi) animals.
Panel E: Normalized intensity of WFA staining around the pMN somata obtained from uninjured (control) and injured (3 dpi, 7 dpi, and 14 dpi) animals.
Panel F: Normalized intensity of WFA staining around the dV2a-INs somata obtained from uninjured (control) and injured (3 dpi, 7 dpi, and 14 dpi) animals.
Figure 5
Panel B: Normalized intensity of WFA staining in uninjured (control), injured (3 dpi), injured (3 dpi) with Vehicle, and injured (3 dpi) with ChABC animals.
Panel C: Adaptation index, resting membrane potential (RMP), mean EPSP frequency, and mean EPSP amplitude obtained from injured (3dpi) and injured (3 dpi) with ChABC pMNs and dV2a-INs.
Panel D: Number of SV2 positive terminals at 3 dpi, 7 dpi, and 14 dpi in injured and injured with ChABC animals.
Panel E: Regeneration index at 7 dpi, 14 dpi, and 21 dpi in injured with Vehicle and injured with ChABC animals. Bridging initiation at 7 dpi of the injured with Vehicle and injured with ChABC animals.
Panel F: Normalized Tubulin intensity at 7 dpi, 14 dpi, and 21 dpi in injured with Vehicle and injured with ChABC animals.
Panel G: Normalized GFP intensity at 7 dpi, 14 dpi, and 21 dpi in injured with Vehicle and injured with ChABC animals.
Panel H: Total distance traveled and immobility index at 7 dpi, 14 dpi, and 21 dpi in injured with Vehicle and injured with ChABC animals.
Panel I: Total time of swimming at 7 dpi, 14 dpi, and 21 dpi in injured with Vehicle and injured with ChABC animals.
Figure S2
Panel A: Resting membrane potential (RMP), input resistance (Rinput), action potential threshold, action potential peak, action potential amplitude, action potential rheobase, action potential half-width duration, and after-hyperpolarization (AHP) amplitude in uninjured (control) and injured (3 dpi, 7 dpi, and 14 dpi) pMNs.
Panel B: Resting membrane potential (RMP), input resistance (Rinput), action potential threshold, action potential peak, action potential amplitude, action potential rheobase, action potential half-width duration, and after-hyperpolarization (AHP) amplitude in uninjured (control) and injured (3 dpi, 7 dpi, and 14 dpi) dV2a-INs.
Figure S3
Panel A: Normalized WFA intensity vs. pMN or dV2a-IN soma size.
Figure S4
Panel A: Normalized intensity of WFA staining in uninjured (control), injured (3 dpi), injured (3 dpi) with 4units of ChABC, and injured (3 dpi) with 8 units of ChABC animals.
Figure S5
Adaptation index, resting membrane potential (RMP), input resistance (Rinput), action potential rheobase, action potential amplitude, after hyperpolarization (AHP) amplitude, action potential half-width duration, action potential threshold, mean EPSP frequency, and mean EPSP amplitude of injured (3 dpi) and injured (3 dpi) with Vehicle.
Figure S6
Panel B: Total distance, number of turns, immobility index, mean acceleration, and percentage of activity of uninjured (control) and injured (3 dpi, 7 dpi, 14 dpi, and 21 dpi) animals that receive the Vehicle.
Panel C: Total distance, number of turns, immobility index, mean acceleration, and percentage of activity of uninjured (control) and injured (3 dpi, 7 dpi, 14 dpi, and 21 dpi) animals that receive the ChABC.
Code/software
Any program that will open a spreadsheet, such as Excel is recommended.
Access information
Other publicly accessible locations of the data:
- Not applicable
Data was derived from the following sources:
- Not applicable
