1986
DOI: 10.1267/ahc.19.205
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Localization of blood group antigens in human pancreas with lectin-horseradish peroxidase conjugates.

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Cited by 25 publications
(8 citation statements)
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“…To mention one essential technical detail, normal serum used to block non-specific binding sites should be preabsorbed with neuraminidase-treated red blood cells in order to avoid anti-TF auto-antibody interference (Springer and Desai 1985). Another point to consider is the observed reactivity of pancreatic acinar cells and gastric mucins from non-secretors with PNA, but not from secretors (Ito et al 1986;Macartney 1986). In general terms, we would like to stress that the combined use of different mAbs and their side-by-side comparison, if necessary in combination with specific glycosidase digestion procedures, are of great importance in obtaining more accurate results.…”
Section: Discussionmentioning
confidence: 99%
“…To mention one essential technical detail, normal serum used to block non-specific binding sites should be preabsorbed with neuraminidase-treated red blood cells in order to avoid anti-TF auto-antibody interference (Springer and Desai 1985). Another point to consider is the observed reactivity of pancreatic acinar cells and gastric mucins from non-secretors with PNA, but not from secretors (Ito et al 1986;Macartney 1986). In general terms, we would like to stress that the combined use of different mAbs and their side-by-side comparison, if necessary in combination with specific glycosidase digestion procedures, are of great importance in obtaining more accurate results.…”
Section: Discussionmentioning
confidence: 99%
“…A glycosylation dependent on blood group systems was only analyzed by histochemical methods in secretory cell types so far: in the human submandibular gland (Ito et al, 1989;Nakayima et al, 1988) and in the pancreas (Ito et al, 1986(Ito et al, & 1990. Since the other cell types of the respiratory surface epithelium-except the secretory goblet cell-do not exhibit such carbohydrate components, it seems likely that the marked substances are a characteristical feature of the status of the basal cells.…”
Section: Discussionmentioning
confidence: 99%
“…Tissues were fixed in 10% formalin for 6-10 days and embedded in paraffin: serial sections were cut at a thickness of 4 l.tm. The blood groups (ABO and Lewis) of the tissue donors were determined as reported previously (Ito et al, 1986(Ito et al, , 1987. The secretor status of the donors was determined by the Lewis blood type or was deduced histochemically from the presence (secretor) or absence (non-secretor) of H antigens in serous cells of the corresponding donor's submandibular glands (Ito et al, 1989a).…”
Section: Methodsmentioning
confidence: 99%
“…Details of the labelled lectin staining methods have been reported previously (Ito et al, 1986). In brief, sections were incubated for 2 h at 4~ in a 20 gg ml -~ solution of lectin conjugate in 0.1 M phosphate buffer (pH 7.2) containing 0.2 M NaC1 and Img ml -~ bovine serum albumin.…”
Section: Methodsmentioning
confidence: 99%