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来自耐受大鼠的骨髓细胞的抗体产生刺激活性。

Antibody production stimulating activity of bone marrow cells from tolerant rats.

作者信息

Mikhailova A A, Madar J, Matousek V, Hraba T

出版信息

Folia Biol (Praha). 1981;27(4):274-8.

PMID:7196848
Abstract

The antibody production stimulating activity of BM cells from SRBC-tolerant and normal rats were studied. Tolerance was induced by repeated injections of SRBC which were begun within 24 h after birth. BM cells obtained from tolerant animals 14-24 days after the last SRBC injection or from normal rats of the same age were used. LN cells from mice immunized with SRBC or BRBC served for the detection of BM activity. Four days after the second injection of antigen, LN cells were removed and cultivated alone or with BM cells from tolerant or control rats for 16 h. After cultivation, immune reaction was estimated by enumeration of indirect PFC. BM cells from SRBC-tolerant rats increased the number of SRBC PFC in the culture more than BM cells from control rats. On the other hand, the stimulatory activity of the BM cells from SRBC-tolerant animals for the BRBC-PFC was lower than that of normal BM cells or it was completely absent. The implications of these findings for the mechanism of the stimulating BM activity are discussed.

摘要

研究了来自对绵羊红细胞(SRBC)耐受和正常大鼠的骨髓(BM)细胞的抗体产生刺激活性。耐受性通过在出生后24小时内开始重复注射SRBC诱导产生。使用在最后一次注射SRBC后14 - 24天从耐受动物获得的BM细胞或来自相同年龄正常大鼠的BM细胞。用SRBC或BRBC免疫的小鼠的淋巴结(LN)细胞用于检测BM活性。在第二次注射抗原后4天,取出LN细胞并单独培养或与来自耐受或对照大鼠的BM细胞一起培养16小时。培养后,通过间接空斑形成细胞(PFC)计数评估免疫反应。来自SRBC耐受大鼠的BM细胞比来自对照大鼠的BM细胞在培养物中增加了SRBC PFC的数量。另一方面,来自SRBC耐受动物的BM细胞对BRBC - PFC的刺激活性低于正常BM细胞或完全不存在。讨论了这些发现对刺激BM活性机制的意义。

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