Association of alcohol intake and female gender with high expression of TMPRSS2 in tongue as potential risk for SARS-CoV-2 infection

  • Sato Kotaro
    Department of Pathology and Biological Responses, Nagoya University Graduate School of Medicine Department of Oral and Maxillofacial Surgery, Nagoya University Hospital
  • Fujii Koki
    Department of Pathology and Biological Responses, Nagoya University Graduate School of Medicine
  • Yamamoto Noriyuki
    Department of Oral and Maxillofacial Surgery, Nagoya University Hospital
  • Ichimura Norihisa
    Department of Oral and Maxillofacial Surgery, Nagoya University Hospital
  • Yamaguchi Satoshi
    Department of Oral and Maxillofacial Surgery, Nagoya University Hospital
  • Yamada Hirohisa
    Department of Oral and Maxillofacial Surgery, Nagoya University Graduate School of Medicine
  • Hibi Hideharu
    Department of Oral and Maxillofacial Surgery, Nagoya University Graduate School of Medicine Center for Low-temperature Plasma Sciences, Nagoya University
  • Toyokuni Shinya
    Department of Pathology and Biological Responses, Nagoya University Graduate School of Medicine Center for Low-temperature Plasma Sciences, Nagoya University

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<p>COVID-19 is pandemic since 2020 and further information is necessary on the risk factors associated with the infection of SARS-CoV-2. As an entry mechanism, SARS-CoV-2 uses angiotensin-converting enzyme 2 (ACE2) as receptor and transmembrane serine protease 2 (TMPRSS2) to activate fusion with host plasma membrane. Because dysgeusia is an early symptom of COVID-19, we here studied the expression of ACE2 and TMPRSS2 in the tongue and the associated tissues of mice and humans with immunohistochemistry and immunoblot analysis. ACE2 expression was low in the human tongue but was observed in the squamous epithelium, perineurium, arterial wall, salivary glands as well as taste buds. In contrast, mice showed high expression. In sharp contrast, TMPRSS2 expression was high in all the cells mentioned above in humans but relatively low in mice except for salivary glands. We then performed semi-quantitation of immunohistochemistry data of human ACE2 and TMPRSS2 and analyzed for age, sex, alcohol intake, and smoking habit with logistic regression analysis. We found that alcohol intake and female gender were the significant risk factors for increasing TMPRSS2 expression. In conclusion, TMPRSS2 is an important factor to be considered regarding SARS-CoV-2 entry and amplification in the oral cavity, which is promoted through drinking habit.</p>

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