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        <datestamp>2025-08-01T00:00:00Z</datestamp>
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          <dc:title>The Role of Adipose-Specific Free Fatty Acid Receptor 2 in Obesity and Associated Metabolic Dysfunction</dc:title>
          <dc:creator>Christine Chioma Nnyamah (22481959)</dc:creator>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Endocrinology</dc:subject>
          <dc:subject>Metabolism</dc:subject>
          <dc:description>Obesity and related metabolic disorders are often characterized by chronic adipose tissue
inflammation, driving systemic insulin resistance and general metabolic dysfunction. Free
Fatty Acid Receptor 2 (FFA2/GPR43) has emerged as a potential modulator of adipocyte
function, inflammation, and metabolism. To investigate the role of FFA2 expressed in the
adipose tissue, we generated adipose-specific FFA2 knockout mice (Adipoq-F2-KO) and
assessed metabolic outcomes under normal chow and high-fat, high-sugar Western diet
conditions, both with and without dietary fiber supplementation. We found that adiposespecific
FFA2 deletion had minimal metabolic consequences under standard dietary
conditions but significantly reduced body weight and adiposity when mice were fed a fibersupplemented
Western diet. Surprisingly, these lighter knockout mice exhibited
heightened adipose inflammation, characterized by increased macrophage infiltration and
pro-inflammatory cytokine expression, independent of differences in food intake or energy
expenditure. Transcriptomic and fecal analyses indicated impaired intestinal lipid
absorption as a primary driver of reduced adiposity, suggesting disrupted adiposeintestinal
communication. Furthermore, in vitro knockdown experiments in adipocytes
revealed that loss of FFA2 impaired adipocyte maturation, lipid storage, and antiinflammatory
signaling. Further studies using intestinal epithelial cells exposed to
adipocyte conditioned media implicated adipose-derived signals in driving intestinal
dysfunction. Collectively, our findings highlight adipose-specific FFA2 as critical in
regulating adipose tissue inflammation, lipid metabolism, and inter-organ communication,
suggesting it as a potential therapeutic target for metabolic disease.</dc:description>
          <dc:date>2025-08-01T00:00:00Z</dc:date>
          <dc:type>Text</dc:type>
          <dc:type>Thesis</dc:type>
          <dc:identifier>10.25417/uic.30425209.v1</dc:identifier>
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          <dc:rights>In Copyright</dc:rights>
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