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FEBS Lett ; 594(20): 3363-3370, 2020 10.
Article in English | MEDLINE | ID: mdl-32880920

ABSTRACT

We used transcriptomic (RNA-seq) analyses to determine whether patients suffering from all types and subtypes of mucopolysaccharidosis (MPS), a severe inherited metabolic disease, may be more susceptible to coronavirus disease 2019 (COVID-19). The expression levels of genes encoding proteins potentially involved in SARS-CoV-2 development were estimated in MPS cell lines. Four genes (GTF2F2, RAB18, TMEM97, PDE4DIP) coding for proteins potentially facilitating virus development were down-regulated, while two genes (FBN1, MFGE8), the products of which potentially interfere with virus propagation, were up-regulated in most MPS types. Although narrowing of respiratory tract and occurrence of thick mucus, characteristic of MPS, are risk factors for COVID-19, transcriptomic analyses suggest that MPS cells might be less, rather than more, susceptible to SARS-CoV-2 infection.


Subject(s)
COVID-19/genetics , Mucopolysaccharidoses/genetics , SARS-CoV-2/physiology , Virus Internalization , Angiotensin-Converting Enzyme 2/genetics , Angiotensin-Converting Enzyme 2/metabolism , COVID-19/metabolism , COVID-19/pathology , COVID-19/prevention & control , Cells, Cultured , Fibroblasts/metabolism , Fibroblasts/pathology , Fibroblasts/virology , Gene Expression Profiling , Genetic Predisposition to Disease , Humans , Mucopolysaccharidoses/metabolism , Mucopolysaccharidoses/pathology , Mucopolysaccharidoses/virology , SARS-CoV-2/pathogenicity , Serine Endopeptidases/genetics , Serine Endopeptidases/metabolism , Transcriptome
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