A. Yuta et al., MUCOGLYCOPROTEIN HYPERSECRETION IN ALLERGIC RHINITIS AND CYSTIC-FIBROSIS, American journal of physiology. Lung cellular and molecular physiology, 17(6), 1997, pp. 1203-1207
There is little information about specific changes in submucosal gland
exocytosis in diseases such as allergic rhinitis (AR), nonallergic rh
initis (NAR), and cystic fibrosis (CF). Nasal lavage fluids were colle
cted from normal, AR, NAR, and CF subjects. Concentrations of lysozyme
, Alcian blue-staining mucoglycoconjugate material (AB-tm), and human
high-molecular-weight; mucoglycoconjugates recognized by the 7F10 muri
ne monoclonal antibody [7F10-immunoreactive mucoglycoconjugates (7F10-
irm)] were measured. AB + m and 7F10-irm were characterized by Sepharo
se-2B column chromatography and glycosidase digestion. 7F10-irm was in
creased in CF (2.4-fold; P = 0.001) and AR (12.7-fold; P = 0.00007) su
bjects. AB+m was increased in CF (1.8-fold; P = 0.049) and AR (1.2-fol
d; P = 0.07) subjects. There were no changes in NAR subjects. On Sepha
rose-2B columns, AB+m peaks were at 1.3-3.0 x 10(6) and 0.36-0.65 x 10
(6) Da. 7F10-irm showed four distinct peaks at 1.5, 1.2, 0.85, and 0.5
3 x 10(6) Da that were nearly identical in both normal and CF samples.
Sialic acid was present in both 7F10-irm and AB+m. 7F10-irm and AB+m
are mutually exclusive sialylated mucoglycoproteins that are significa
ntly induced in AR and CF but not in NAR.