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          <dc:title>&lt;p&gt;LPS-induced alterations in intestinal transport and enteroendocrine marker expression in pSIOs.&lt;/p&gt;</dc:title>
          <dc:creator>Sumin Park (1418677)</dc:creator>
          <dc:creator>Boram Lee (549836)</dc:creator>
          <dc:creator>Dahye Kim (4750968)</dc:creator>
          <dc:creator>Sheet Sunirmal (25157743)</dc:creator>
          <dc:creator>Min Gook Lee (25157746)</dc:creator>
          <dc:creator>Haesun Lee (13907847)</dc:creator>
          <dc:creator>Sun A. Ock (17671438)</dc:creator>
          <dc:creator>Jae Gyu Yoo (18291035)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Science Policy</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>potentially reducing reliance</dc:subject>
          <dc:subject>cell models fail</dc:subject>
          <dc:subject>adult jejunum stimulated</dc:subject>
          <dc:subject>functional categories associated</dc:subject>
          <dc:subject>bile acid signaling</dc:subject>
          <dc:subject>div &gt;&lt; p</dc:subject>
          <dc:subject>cytokine gene expression</dc:subject>
          <dc:subject>studying intestinal inflammation</dc:subject>
          <dc:subject>intestinal tract</dc:subject>
          <dc:subject>associated diseases</dc:subject>
          <dc:subject>receptor signaling</dc:subject>
          <dc:subject>inflammatory signaling</dc:subject>
          <dc:subject>vitro &lt;/</dc:subject>
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          <dc:subject>transcriptome analysis</dc:subject>
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          <dc:subject>related pathways</dc:subject>
          <dc:subject>proteins involved</dc:subject>
          <dc:subject>physiologically relevant</dc:subject>
          <dc:subject>nutrient transport</dc:subject>
          <dc:subject>major threat</dc:subject>
          <dc:subject>inflammatory stress</dc:subject>
          <dc:subject>induced alterations</dc:subject>
          <dc:subject>increased tlr4</dc:subject>
          <dc:subject>including enrichment</dc:subject>
          <dc:subject>immunofluorescence staining</dc:subject>
          <dc:subject>findings demonstrate</dc:subject>
          <dc:subject>enriched pathways</dc:subject>
          <dc:subject>barrier maintenance</dc:subject>
          <dc:subject>barrier integrity</dc:subject>
          <dc:subject>animal testing</dc:subject>
          <dc:subject>analyzing changes</dc:subject>
          <dc:subject>altered expression</dc:subject>
          <dc:subject>3rs principle</dc:subject>
          <dc:description>&lt;p&gt;(A) Immunofluorescence of pSIOs stained with DAPI (blue) to visualize nuclei and immunolabeled for SGLT1 (green), PEPT1 (green), GLUT2 (green), TGR5 (red), and GLP-1 (green). Representative untreated (upper rows) and LPS-treated (lower rows) organoids are shown. Untreated organoids exhibited distinct localization of SGLT1, PEPT1, GLUT2, and TGR5 along the epithelial membrane with strong expression and cytoplasmic GLP-1 expression in scattered enteroendocrine-like cells within the epithelial layer. LPS-treated organoids exhibited reduced expression intensity, irregular protein distribution, and partial loss of membrane localization. Enlarged views of the yellow boxed regions further highlight differences in expression patterns and subcellular localization between untreated and LPS-treated organoids. Images are representative of three independent biological replicates (n = 3), with at least five organoids analyzed for each treatment condition in each biological replicate. Scale bars: 50 μm. (B) qRT-PCR analysis showing significant alterations in nutrient transporter and enteroendocrine-related gene expression following LPS treatment. Decreased &lt;i&gt;SLC5A1&lt;/i&gt; (SGLT1) and &lt;i&gt;SLC15A1&lt;/i&gt; (PEPT1) expression and increased &lt;i&gt;SLC2A2&lt;/i&gt; expression were observed after LPS exposure. Among enteroendocrine-related genes, GPBAR1 expression was markedly decreased, whereas GCG (the precursor gene of GLP-1) expression was significantly increased after LPS exposure.Data are presented as the mean ± SD from three biological replicates (n = 3); each biological replicate was analyzed using five technical replicates. **&lt;i&gt;p&lt;/i&gt; &lt; 0.01, ***&lt;i&gt;p&lt;/i&gt; &lt; 0.001.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T17:30:26Z</dc:date>
          <dc:type>Image</dc:type>
          <dc:type>Figure</dc:type>
          <dc:identifier>10.1371/journal.pone.0359086.g005</dc:identifier>
          <dc:relation>https://figshare.com/articles/figure/_p_LPS-induced_alterations_in_intestinal_transport_and_enteroendocrine_marker_expression_in_pSIOs_p_/34048156</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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