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Mucins and their O-Glycans from human bronchial epithelial cell cultures.

Holmén, Jessica, 1971 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
Karlsson, Niclas G., 1966 (författare)
Abdullah, Lubna H (författare)
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Randell, Scott H (författare)
Sheehan, John K (författare)
Hansson, Gunnar C., 1951 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
Davis, C William (författare)
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 (creator_code:org_t)
American Physiological Society, 2004
2004
Engelska.
Ingår i: American journal of physiology. Lung cellular and molecular physiology. - : American Physiological Society. - 1040-0605 .- 1522-1504. ; 287:4
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • A longstanding question in obstructive airway disease is whether observed changes in mucin composition and/or posttranslational glycosylation are due to genetic or to environmental factors. We tested whether the mucins secreted by second-passage primary human bronchial epithelial cell cultures derived from noncystic fibrosis (CF) or CF patients have intrinsically different specific mucin compositions, and whether these mucins are glycosylated differently. Both CF and non-CF cultures produced MUC5B, predominantly, as judged by quantitative agarose gel Western blots with mucin-specific antibodies: MUC5B was present at approximately 10-fold higher levels than MUC5AC, consistent with our previous mRNA studies (Bernacki SH, Nelson AL, Abdullah L, Sheehan JK, Harris A, William DC, and Randell SH. Am J Respir Cell Mol Biol 20: 595-604, 1999). O-linked oligosaccharides released from purified non-CF and CF mucins and studied by HPLC mass spectrometry had highly variable glycan structures, and there were no observable differences between the two groups. Hence, there were no differences in either the specific mucins or their O-glycans that correlated with the CF phenotype under the noninfected/noninflammatory conditions of cell culture. We conclude that the differences observed in the mucins sampled directly from patients are most likely due to environmental factors relating to infection and/or inflammation.

Nyckelord

Adolescent
Adult
Bronchi
Bronchiolitis Obliterans
Carbohydrate Sequence
Cells
Cultured
Electrostatics
Female
Genotype
Humans
Kinetics
Male
Middle Aged
Molecular Sequence Data
Mucins
chemistry
physiology
Oligosaccharides
chemistry
Polysaccharides
chemistry
physiology
Respiratory Mucosa
cytology
pathology
physiology
physiopathology

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