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        <datestamp>2025-08-01T00:00:00Z</datestamp>
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          <dc:title>Identifying Diagnostic Biomarkers: Gene Expression Profiling Leptin in Dental Pulp Tissue</dc:title>
          <dc:creator>Christopher Greenwaldt (22481830)</dc:creator>
          <dc:subject>Health Sciences</dc:subject>
          <dc:subject>Dentistry</dc:subject>
          <dc:description>Recent studies emphasized the role of leptin/leptin receptor (LEP/LEPR) in normal and inflammatory conditions of dental pulp tissues. LEP/LEPR activity is linked to potential immunomodulation responses during bacterial-induced inflammatory conditions. Additionally, there is substantial association of LEP in dental pulp stem cells (DPSCs), odontoblast differentiation/function and mineralization processes. The objective of this study is to investigate differential leptin gene expression in hypoxic (inflammatory) conditions.
DPSCs were isolated from healthy adult third molars, supplemented with 1% serum containing media or osteogenic media, and cultured in hypoxic (3%) or normoxic (21%) conditions for 21-days. Later, DPSCs collected were extracted for mRNA isolation. The mRNA was sequenced using NextSeq Illumina and was analyzed using the ERGO transcription tool DESeq2 (P&lt;0.05) statistical method to determine differences in transcription and subsequent translation between groups. The count data was imported into R-package for analysis and sequence mapping to the appropriate gene.
The genes and pathways were identified in KEGG pathways overlaying expression values. Over-expressed (p&lt;0.05) genes include ACSL1, LEP, LEPR and PRKAA2 and under-expressed (p&lt;0.05) genes include MAPK8, NFKBIE, RELA.
DPSCs in hypoxic conditions shows down-regulation of AMPK signaling, which is related to cellular energy, transcription factors p65, NF-kappa-B and MAP Kinases associated with transcription regulation and differentiation. Up regulation of LEP/LEPR is associated with fat metabolism and both immune and inflammatory responses. Therefore, LEP signaling is an important regulator of DPSCs function. Furthermore, deciphering LEP/MAPK/Insulin signaling pathways in inflammatory condition of dental pulp could lead to new and more effective treatments for pulpitis and apical periodontitis.</dc:description>
          <dc:date>2025-08-01T00:00:00Z</dc:date>
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          <dc:identifier>10.25417/uic.30425056.v1</dc:identifier>
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          <dc:rights>In Copyright</dc:rights>
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