Röpke C, Everett N B
Am J Anat. 1976 Mar;145(3):395-408. doi: 10.1002/aja.1001450307.
The proliferative kinetics of the intraepithelial lymphocytes (IL) of the mouse intestine have been evaluated. By inducing mitotic arrest it was found that large IL - constituting about 50% of the IL - showed a mitotic rate of 2.3. Autoradiographic results obtained after two different schedules of 3H-thymidine injections showed that 30% of the large IL were in DNA synthesis, and that the large IL were renewed at a rate comparable to that of blast cells from Peyer's patches, mesenteric lymph nodes and thoracic duct lymph. The small IL were renewed very rapidly compared to small lymphocytes of peripheral lymphoid tissues, although small lymphocytes with lifespans of several weeks were also present in the epithelial sheet. By the use of intestinal perfusion, in vivo, it was estimated that the loss of lymphocytes from intestinal villi into the lumen of the gut was negligible, and it is concluded that the most probable kinetic model for the majority of IL is: B and T lymphoblasts invade the epithelium and undergo mitosis. B lymphoblasts give rise predominantly to plasma cells, and T lymphoblasts give rise to small lymphocytes - probably long-lived - which reenter the circulation.
已对小鼠肠道上皮内淋巴细胞(IL)的增殖动力学进行了评估。通过诱导有丝分裂停滞发现,占IL约50%的大型IL的有丝分裂率为2.3。在两种不同的³H-胸腺嘧啶核苷注射方案后获得的放射自显影结果表明,30%的大型IL处于DNA合成状态,并且大型IL的更新速率与派尔集合淋巴结、肠系膜淋巴结和胸导管淋巴中的母细胞相当。与外周淋巴组织的小淋巴细胞相比,小型IL更新非常迅速,尽管上皮层中也存在寿命为数周的小淋巴细胞。通过体内肠灌注估计,肠道绒毛中的淋巴细胞向肠腔的丢失可忽略不计,并且得出结论,大多数IL最可能的动力学模型是:B和T淋巴母细胞侵入上皮并进行有丝分裂。B淋巴母细胞主要产生浆细胞,T淋巴母细胞产生小淋巴细胞——可能是长寿的——这些小淋巴细胞重新进入循环。