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        <datestamp>2026-09-28T04:30:13Z</datestamp>
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          <dc:title>Supplementary file 1_Divergent cellular responses to sciatic nerve crush versus transection: bilateral MYCN induction and distinct DRG neuronal responses.docx</dc:title>
          <dc:creator>Shilian Zhou (25119468)</dc:creator>
          <dc:creator>Ziyan Huang (3863497)</dc:creator>
          <dc:creator>Zhongyuan Lin (651801)</dc:creator>
          <dc:creator>Jingwei Chen (1578331)</dc:creator>
          <dc:creator>Xinyu Zhang (14029)</dc:creator>
          <dc:creator>Diya Wang (5018522)</dc:creator>
          <dc:creator>Haihua Shu (12019018)</dc:creator>
          <dc:creator>Fang Ye (112854)</dc:creator>
          <dc:subject>Cellular Interactions (incl. Adhesion, Matrix, Cell Wall)</dc:subject>
          <dc:subject>ATF3</dc:subject>
          <dc:subject>bilateral spinal response</dc:subject>
          <dc:subject>MYCN</dc:subject>
          <dc:subject>nerve regeneration</dc:subject>
          <dc:subject>peripheral nerve injury</dc:subject>
          <dc:subject>sciatic nerve axotomy</dc:subject>
          <dc:subject>sciatic nerve crush</dc:subject>
          <dc:subject>sensory dysfunction</dc:subject>
          <dc:description>Introduction&lt;p&gt;Peripheral nerve injuries can produce regenerative or persistent-disconnection outcomes depending on the injury modality, but the underlying cellular responses and their effects on the central nervous system remain incompletely defined.&lt;/p&gt;Methods&lt;p&gt;We compared sciatic nerve crush (SNC; axonotmesis) and sciatic nerve transection (SNT; neurotmesis) in wild-type, AdvCre;Ai14, and MYCN-eGFP reporter mice. Longitudinal assessments included functional recovery, neuronal injury responses marked by ATF3, IB4-positive sensory-neuron responses, dorsal-horn microglial activation, and spinal MYCN-eGFP signal.&lt;/p&gt;Results&lt;p&gt;SNC was associated with partial, measure-specific functional recovery, a transient and self-limited ATF3 response, and a limited reduction in IB4-positive neuronal profiles. In contrast, SNT produced persistent axotomy-associated neuronal stress, a reduction in IB4-positive neuronal profiles, and more protracted dorsal-horn microglial activation. MYCN-eGFP intensity was significantly increased above sham levels bilaterally in spinal ventral-horn neurons after both SNC and SNT at postoperative day 7 (POD7), with the greatest acute amplitude observed after SNC. From POD7 to POD14, MYCN-eGFP intensity declined by more than 90% after SNC but by approximately 60% after SNT, indicating distinct temporal patterns between the two injury modalities.&lt;/p&gt;Discussion&lt;p&gt;SNC and SNT engage overlapping but quantitatively and temporally distinct cellular programs, including modality-specific dorsal root ganglion neuronal responses associated with functional recovery. These findings refine the interpretation of two widely used peripheral nerve injury models and identify bilateral spinal MYCN-eGFP dynamics as a candidate cellular readout for future mechanistic investigation.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-28T04:30:13Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fncel.2026.1922426.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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