<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE215132" accession="SRP401792">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP401792</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA888974</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE215132</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Effect of Ptpn2 KO and IFN? on axon regeneration</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>To investigate the function of Ptpn2, IFN? and cGAS on axon regeneration, we performed gene transcription profiling of dorsal root ganglion neurons from 5 groups (WT, cKO, WT injured, cKO injured, RU521 injured) and retinal ganglion cells from 4 groups (WT, IFN?, cKO, IFN?+cKO). Overall design: For DRG experiment, cGAS inhibitor RU521 was injected to the sciatic nerve of wildtype mice. Nerve samples were collected 3 days after injury and RNA was extracted for sequencing. For RGC experiment, AAV-Cre or GFP was injected to the eyes of Ptpn2 flox mice 2 weeks before optic nerve injury. IFN? was injected to the eyes right after injury. Retinal ganglion cells (WT,IFN?,cKO,cKO+IFN?) were collected 3 days after injury and RNA was extracted for sequencing.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE215132</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>36370710</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
