THE pH RANGE OF THE DIAZOSAFRANIN REACTION OF RAT AND OTHER MAST CELLS

1973 ◽  
Vol 21 (5) ◽  
pp. 441-447 ◽  
Author(s):  
R. D. LILLIE ◽  
PHILIP PIZZOLATO ◽  
LINDA L. VACCA ◽  
ROY A. CATALANO ◽  
PATRICIA T. DONALDSON

5-Hydroxytryptophan and 5-hydroxytryptamine (5-HT) give strong red azo coupling colors with fresh p-nitrodiazobenzene (fast red GG) at coupling pH levels of 3-9. Tyrosine, histidine, histamine, adrenaline, noradrenaline, dopa, dopamine and tryptophan give strong red colors at pH 7-9, weakening to orange and yellow at pH 5-6 and negative below. Tryptophan gives weak orange-yellow to about pH 4. Rat mast cells color deep red with diazosafranin at pH 3-8. Protein colors pink to red at pH 7-8, weaker at 5-6, and remains almost uncolored below that. Preoxidation with 10 min 1% H5IO6, 2 hr 0.1 M FeCl3, 3 hr 5% K2Cr2O7 or 1 hr 3°C 10% I2/CH3OH does not prevent the diazosafranin reaction of rat mast cells. Periodic acid does not inhibit in vitro azo coupling of 5-HT or 1-naphthol, that of noradrenaline is prevented, and can be restored by reduction with Na2S2O5 or Na2S2O3. Azo coupling of enterochromaffin and adrenal medulla is prevented by these oxidations and restored by Na2S2O4 reduction. Diazosafranin staining of mast cells is not extracted by 24 hr 0.24 N HCl/70% alcohol. Safranin and other cationic dye staining of rat mast cells resists aqueous 0.1 N HCl some hours, largely disappearing at 24 hr, and is removed by 5-15 min in 0.12 N HCl/7O% alcohol. At pH 1 0.1% toluidine blue colors rat mast cells deep violet; when superimposed after acid diazosafranin the red mast cells assume a deep purple, intermediate color. Since in extended use of the method pH 3 diazosafranin colors only bilirubin casts, hematoidin and dog, rat, mouse and gerbil mast cells, and not monkey, most human or lead and mercury fixed guinea pig mast cells, it is suggested that the method is showing 5-HT in rat mast cells. The occasional reaction of human mast cells may be due to pathologic presence of that substance in these cells.

1974 ◽  
Vol 4 (3) ◽  
pp. 204-204 ◽  
Author(s):  
P. Stahl Skov ◽  
S. Norn
Keyword(s):  

1979 ◽  
Vol 181 (3) ◽  
pp. 623-632 ◽  
Author(s):  
B Jasani ◽  
G Kreil ◽  
B F Mackler ◽  
D R Stanworth

Structure-activity studies have been performed on a series of naturally occurring and ‘tailor-made’ polypeptides, by measurement of ability to induce selective histamine release from normal rat peritoneal mast cells in vitro. Compounds investigated include corticotropin and melittin derivatives, mast-cell-degranulating peptide from bee venom, polymyxin B, bradykinin and various synthetic poly(amino acids) and short-chain peptides. It was confirmed that a cluster of four basic residues (lysine or arginine) was optimal for histamine release by corticotropin and melittin polypeptides, provided that the C-terminal carboxyl group was substituted (by, for instance, amidation). In contrast, the presence of a free C-terminal carboxyl group or nearby dicarboxylic acid residues led to a considerable diminution in histamine-releasing activity. Likewise, polypeptides comprised essentially of acidic amino acids were inactive. On the basis of these observations it has been possible to predict that synthetic peptides comprising a particular sequence within the Fc region of human immunoglobulin E, the immunoglobulin class particularly involved in mediation of allergic reactions of the immediate type, would possess potent histamine-releasing activity when similarly made to react with normal rat mast cells. The further study of such a structure should throw new light on the molecular basis of allergen-antibody triggering of mast cells.


1980 ◽  
Vol 191 (1) ◽  
pp. 233-237 ◽  
Author(s):  
P D Roy ◽  
D M Moran ◽  
V Bryant ◽  
R Stevenson ◽  
D R Stanworth

Previous studies on histamine release by corticotropin peptides and melittin peptides were extended, leading to the identification of a synthetic peptide intermediate, Lys(Z)-Arg(NO2)-Arg(NO2)OMe, (I) as an active non-cytolytic histamine releaser from rat mast cells. However, significant differences in the releasing capacity of optical isomers of this compound, and of Lys-Lys-Arg-ArgOMe [methyl ester of corticotropin-(15-18)-tetrapeptide; ‘basic core’] were observed, with the L-forms being markedly more active. A study of various analogues of the tripeptide compound (I) indicated that the structural basis for mast-cell triggering by such peptidic agents was highly specific. The relevance of these observations to the immunologically induced histamine-release processes is discussed.


1982 ◽  
Vol 114 (3) ◽  
pp. 467-469 ◽  
Author(s):  
P. G. KRÜGER ◽  
P. AAS ◽  
J. ONARHEIM ◽  
K. B. HELLE
Keyword(s):  

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