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    <identifier>10.57760/sciencedb.07220</identifier>
    <datestamp>2023-09-28T09:06:19Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2023-09-28</dc:date>
  <dc:title>RNA sequencing analysis of LPS-treated BMDMs from Nrp2fl/flLyz2-cre and Nrp2fl/fl mice</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.07220</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Primary bone marrow-derived macrophages (BMDMs) were isolated from femurs of Nrp2fl/flLyz2-cre and Nrp2fl/fl mice and cultured in DMEM supplemented with 10% FBS, penicillin-streptomycin (50 U/mL) and 20% L929 supernatant as a source of M-CSF for 7 days maturation. After 7 days, BMDMs were treated with 200 ng/ml LPS for 18 h in vitro. After polarization, BMDMs were collected for RNA sequencing analysis. All the animal experiments were approved by Institutional Animal Care and Use Committee of Sichuan University.UID RNA-seq experiment and high through-put sequencing and data analysis were conducted by Seqhealth Technology Co., LTD (Wuhan, China). Briefly, total RNAs were extracted from samples using TRIzol Reagent. 2 &amp;mu;g total RNAs were used for stranded RNA sequencing library preparation using KC-DigitalTM Stranded mRNA Library Prep Kit for Illumina&amp;reg; following the manufacturer&amp;rsquo;s instruction.&amp;nbsp;Raw sequencing data was first filtered by Trimmomatic (version 0.36). Low-quality reads were discarded, and the reads contaminated with adaptor sequences were trimmed. Clean Reads were further treated with in-house scripts to eliminate duplication bias introduced in library preparation and sequencing.&amp;nbsp;The de-duplicated consensus sequences were used for standard RNA-seq analysis.&amp;nbsp;Reads mapped to the exon regions of each gene were counted by featureCounts (Subread-1.5.1; Bioconductor) and then RPKM was calculated. Genes differentially expressed between groups were identified using the edgeR package (version 3.12.1). A p-value&amp;thinsp;cutoff of 0.05 and Fold-change cutoff of 2 were used to judge the statistical significance of gene expression differences.&amp;nbsp;</dc:description>
  <dc:subject>NRP2; macrophage; colitis; NF-κB ; TNF</dc:subject>
  <dc:creator>Tong Li</dc:creator>
  <dc:creator>Zhiyong Miao</dc:creator>
  <dc:creator>Jingjing Ran</dc:creator>
  <dc:creator>Min Yang</dc:creator>
  <dc:creator>Dachao Mou</dc:creator>
  <dc:creator>Ke Jin</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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