THE ?segregation apparatus? of the amphibian erythrocyte and its possible relation to the Golgi apparatus
โ Scribed by Dawson, Alden B.
- Publisher
- John Wiley and Sons
- Year
- 1928
- Tongue
- English
- Weight
- 919 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0003-276X
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โฆ Synopsis
Recently, while studying preparatioiis of thc mesoiicpliros of Necturus, which had h e n successfully prepared accordiiig to the ?Jassoiio\r-I'olatclicv method for the demoiistratioii of the Golgi apparatns, my attention was nttiwted to definite hlackcnetl granules present in the erythrocytes which were lying within the l~loocl vessels of tliis organ. The resem1)lance of tlicsc structures to those demonstrated by Jordan '25) in the erythrocytes of tlie leopard frog b y mcaiis of the vital dyes, neutral red and hrilliant cresyl blue, led me to uiidertake the present study. M y interest in this problem was also greatly stimulated hy tlie recent wo1-B of CYovell and Scott ( 'as), ~vliose firidiiigs support the h>Tpothesis advanced by Parat and his coworkers tliat the Golgi apparatns results from tlie treatment of neutral red-staiiiahlc granules with silver aiitl osmic acid.
-Jordan, employing lieu tral-red stainiiig according to the method described hy Sabin (%), found that, after a period ranging from one-half to a full hour, the erythrocytes of the frog showed a variable iiumhcr of small red-stained spherical granules and globules (test fig. A,a ) . During a period of from two to six hours these globules progressively enlarged (text fig. A, b) many hecomiiig ari-angetl in some cells to form a sort of crown immediately about the nucleus. I n oiie prepa-
๐ SIMILAR VOLUMES
M a w College ## THREE FIGURES The methods employed were based primarily on the work of Scott (,as) on the vital staining of blood cells.
Intracellular glycosyltransferase protein expression can be assessed by flow cytometry. We report the detectability of the Golgi associated b1,4 galactosyltransferase (GT) and a2,6 sialyltransferase (ST) upon permeabilization in Jurkat and EBV-JY cells representing a T-and B-lymphoid cell line, resp