CELL PROLIFERATION IN GERMINAL CENTERS OF RAT SPLEEN
CELL PROLIFERATION IN GERMINAL CENTERS OF RAT SPLEEN
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DOI:
10.1111/j.1749-6632.1964.tb40692.x
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发表时间:
1964-01-01
影响因子:
5.2
通讯作者:
KESSE, M
中科院分区:
文献类型:
--
作者:
FLIEDNER, TM;ROBERTSON, JS;KESSE, M
The purpose of this paper is to present data which gives some insight into the rate of cell proliferation within the lymphatic nodules of the rat’s spleen. In this study, the technique of labeling DNA with the specific precursor, tritiated thymidine, was used. The observations were made on the Malpighian corpuscles of the spleen, utilizing autoradiographic methods.The lymphatic nature of the Malpighian corpuscles was first recognized by Kolliker in 1855.’Lymphatic nodules are observed in various forms, but the most characteristic histological appearance consists of an aggregation of cells in which a central zone of pale-staining cells can be distinguished from a zone of darkstaining, closely packed smaller cells. This central zone was named “Keimzentrum” or the “germinal center” by Flemming in 1885.2 Flemming observed the high mitotic activity in the germinal centers and felt that this area was actively forming lymphocytes. Other terms that have been used for the germinal center are “secondary nodule” or “Innenraum.” The germinal center is surrounded by dark staining small cells and has been termed “mantle zone” or “marginal zone.” The mantle zone is surrounded, in turn, by a well-defined circular area of larger cells (mixed large lymphocytes, histiocytes, and perhaps other cells). This zone has also been called “marginal layer,”“Knotchenrandzone,” and “Follikel-Aussenzone.” The cells in this zone are arranged more loosely than in the mantle zone. Since the original description of lymphatic nodules by Flemming, various ideas have been advanced in respect to their possible function. The question of their function remains a matter of continuing controversy. Some investigators have supported Flemming’s suggestion that the pale centers of the nodules are “germinal centers” for the formation of new lymphocytes, although it is well known that these are not the only sites of new cell prod~ ction.~-~ This concept was challenged by Marchand’in 1913. He pointed out that the germinal centers are usually sharply demarcated. This makes it difficult to visualize potential genetic relations between “germinal center” cells and the surrounding small lymphocytes. Since then, numerous experimental and pathological studie~~,~ have been reported in support of Marchand’s doubts. Hellmanlo suggested that a major function of the germinal centers was to act as “reaction centers” against toxins. There is also ample evidence that germinal centers are produced as a reaction to bacterial infections and repetitive antigenic~ timulation.~~-~~ White, 14 however, produced evidence that germinal centers are produced only after induction of the anamnestic (secondary response) and not after the primary antigenic stim~ lus.’~ Most recently this has been conclusively demonstrated by Cottier et The high mitotic index of germinal centers signifies that there is a significant production of new cells. Whether these newly formed cells in the germinal centers should be