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    <responseDate>2026-10-13T07:17:29Z</responseDate>
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    <identifier>10.57760/sciencedb.03324</identifier>
    <datestamp>2022-10-17T09:42:36Z</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>2022-10-17</dc:date>
  <dc:title>RNA SEQ data of mouse CD8+ Teff treated with LA/LC</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.03324</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>CD8+ T cells derived from mouse spleen were activated by CD3/28 in vitro and divided into the following four groups. 1. The control group was treated with solvent (water). 2. Lactic acid treatment group was treated with 10mM lactic acid for 3 hours; 3. Lithium carbonate group was treated with 1mM lithium carbonate for 3 hours; 4. The lactate/lithium carbonate combined treatment group was treated with 1mM lithium carbonate combined with 10mM lactate for 3 hours. The samples were lysed with Trizol and then total RNA was extracted for RNASEQ sequencing. Sample TE11-13 was CTR2 in the control group; Sample LA11-13 was LAC2 in lactate treatment group. LC11-13 was LCcase2 in lithium carbonate treatment group. Sample LALC11-13 was LALCcase2 in the lactate/lithium carbonate combined treatment group</dc:description>
  <dc:subject>CD8; LACTATE ACID; MOUSE; lithium carbonate</dc:subject>
  <dc:creator>Tang Liang</dc:creator>
  <dc:creator>YAO YAO TAN</dc:creator>
  <dc:creator>BO HUANG</dc:creator>
  <dc:creator>JING WEI MA</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:relation>http://www.doi.org/10.1038/s41590-023-01738-0</dc:relation>
  <dc:publisher>Science Data Bank</dc:publisher>
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