posted on 2020-10-06, 11:51authored byAda AdminAda Admin, Sara RA Wijnant, Merel Jacobs, Hannelore P Van Eeckhoutte, Bruno Lapauw, Guy F Joos, Ken R Bracke, Guy G Brusselle
Increased expression
of pulmonary ACE2, the SARS-CoV-2 receptor, could contribute to increased infectivity
of COVID-19 in subjects with diabetes, but ACE2 expression has not been studied
in lung tissue of subjects with diabetes. We therefore studied ACE2 mRNA and
protein expression in lung tissue samples of patients with and without diabetes
that were collected between 2002 and 2020 from patients undergoing lobectomy for lung tumors. For
RT-PCR analyses, samples from 15 subjects with diabetes were compared to 91 randomly
chosen control samples. For
immunohistochemical staining, samples from 26 subjects with diabetes were
compared to 66 randomly chosen control samples. mRNA expression of ACE2 was measured by quantitative RT-PCR. Protein
levels of ACE2 were visualized by immunohistochemistry on paraffin-embedded
lung tissue samples and quantified in alveolar and bronchial epithelium. Pulmonary ACE2 mRNA expression was not different between subjects with or
without diabetes. In contrast, protein
levels of ACE2 were significantly increased in both alveolar tissue and
bronchial epithelium of patients with diabetes as compared with control
subjects, independent of smoking, COPD, BMI, RAAS-inhibitor use and other
potential confounders. To conclude, we show increased bronchial and alveolar ACE2 protein
expression in patients with diabetes. Further research is needed to elucidate
whether up-regulation of ACE2 expression in airways and lungs has consequences
on infectivity and clinical outcomes of COVID-19.
Funding
The research described in this article was supported by the Concerted Research Action of the Ghent University (BOF/GOA 01G00819) and by the Fund for Scientific Research in Flanders (FWO Vlaanderen, G052518N and 3G037618, and EOS‐contract G0G2318N).