SOME ASPECTS OF FEULGEN REACTION IN SITU

被引:10
作者
GHOSH, S
GHOSH, I
机构
[1] Institute for Experimental Cancer Research, German Cancer Research Centre, Heidelberg
来源
HISTOCHEMIE | 1969年 / 19卷 / 02期
关键词
D O I
10.1007/BF00281097
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytological observations combined with studies on absorption spectra of Feulgen stained normal and lipid - extractet HeLa and ehrlich-Lettré mouse ascites cells were performed after fixation of the cells as well in neutral formaldehyde as in Serra fixative. The effects of formaldehyde treatment of the stained cells to substitute all the free amino groups of DNA bond pararosaniline molecules, were also studied. The results obtained by using DNA samples containing 2% protein and relatively free from protein, led to the conclusion that after acid hydrolysis for a short period purines in DNA become splitted and these released aldehydes react with one or two amino groups of pararosaniline, a triphenylmethane dye (according to the arrangement of purines and pyrimidines in the helices). Some protein molecules also take part in the reaction and substitute some of the free amino groups of DNA bound pararosaniline. Peulgen stained cells fixed in Serra fixative show an absorption maximum at 546-550 mμ. Under appropriate conditions, as in cells fixed in formaldehyde, other substances e.g. phospholipids and lipoproteins interfere with the reaction by substituting most of the free amino groups of DNA bound pararosaniline molecules. It has been argued that in histochemical reactions monosubstituted pararosaniline molecules should be coloured and further substitution of free amino groups of pararosaniline, bound in DNA helices, does not change the intensity of the colour, but gives a shift in the wavelength of the absorption spectra. It has been suggested that the differential response of the nucleoli to the Feulgen-reaction, depending on whether the cells were fixed in formaldehyde or in Serra fixative, may be due to the formation of a protecting shield around the finely distributed intranucleolar chromatin strands, when formaldehyde is being used. After this fixation lipoproteins and other lipids, present in a relatively high percentage and closely associated with the intranucleolar chromatin strands, are especially well preserved. Evidences have been put foreward in support of the amino alkylsulfonic acid theory of Rumpf (1935) and Hörmannet al. (1958) whereas the amino sulfinic acid theory to explain the Schiffs reaction (Wieland and Scheuing, 1921) was shown not to be in agreement with our results. © 1969 Springer-Verlag.
引用
收藏
页码:165 / +
页数:1
相关论文
共 36 条
[1]   UBER CHROMATIN UND DNS-SYNTHESE IM NUCLEOLUS - ELEKTRONENMIKROSKOPISCHE, AUTORADIOGRAPHISCHE UND LICHTMIKROSKOPISCHE UNTERSUCHUNGEN AN LEBERZELLEN VON RATTEN [J].
ALTMANN, HW ;
STOCKER, E ;
THOENES, W .
ZEITSCHRIFT FUR ZELLFORSCHUNG UND MIKROSKOPISCHE ANATOMIE, 1963, 59 (01) :116-133
[2]   ZUM PROBLEM DER NUCLEOLAREN STOFFABGABE - ELEKTRONENMIKROSKOPISCHE UNTERSUCHUNGEN AM PANKREAS DER WEISSEN MAUS [J].
BANNASCH, P ;
THOENES, W .
ZEITSCHRIFT FUR ZELLFORSCHUNG UND MIKROSKOPISCHE ANATOMIE, 1965, 67 (05) :674-&
[3]   SOME OBSERVATIONS ON THE REACTION OF SCHIFF REAGENT WITH ALDEHYDES [J].
BARKA, T ;
ORNSTEIN, L .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1960, 8 (03) :208-213
[4]  
Bauer H., 1932, Z ZELLFORSCH MIKROSK, V15, P225
[5]  
Caspersson T, 1932, BIOCHEM Z, V253, P97
[6]  
CHAVEN J, 1960, EXP CELL RES, V20, P150
[7]  
CHAYEN J., 1959, EXPTL CELL RES, V6, P115
[8]   Microscopic chemical varification of nucleic acid in the types of thymonucleic acid and its dependent elective colorisation of the cell core in microscopic preparations. [J].
Feulgen, R ;
Rossenbeck, H .
HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1924, 135 (5/6) :203-248
[9]   MECHANISM OF SCHIFF REACTION AS STUDIED WITH HISTOCHEMICAL MODEL SYSTEMS [J].
HARDONK, MJ ;
VANDUIJN, P .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1964, 12 (10) :748-&
[10]   STUDIES ON FEULGEN REACTION WITH HISTOCHEMICAL MODEL SYSTEMS [J].
HARDONK, MJ ;
VANDUIJN, P .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1964, 12 (10) :758-&