Palacios R, Leu T
Cell Immunol. 1986 Jul;100(2):532-40. doi: 10.1016/0008-8749(86)90051-1.
We show here that the combination of Concanavalin A (Con A), phorbol myristate acetate (PMA), and Ionomycin (Iono) reproducibly stimulated splenocytes from Nu/Nu mice and bone marrow cells from both normal and Nu/Nu mice to secrete interleukin 3 (IL-3) in vitro. IL-3 was measured by its property of supporting the growth of four different clones known to grow only in IL-3. None of the agents indicated above nor several other types of stimuli tested could induce the cells to secrete IL-3 activity. IL-3 activity from induced cells of either tissue was detected after 24 hr of culture, peaked at 48 hr and either declined by 72-96 hr of culture (bone marrow cells) or remained relatively constant through the 4-day culture period (splenocytes). The cells participating in the production of IL-3 activity in Nu/Nu spleen were THY1+, L3T4-, LyT2-, B-220-, J11d-, Ia-, and those in the marrow from either normal or Nu/Nu mice were THY1+, J11d+, L3T4-, LyT2-, B-220-, Ia-. Finally, we present evidence that Ia-positive cells negatively regulate the production of IL-3 activity by both splenocytes and marrow cells. We conclude that Nu/Nu splenocytes and bone marrow cells from both normal and Nu/Nu mice can secrete IL-3 activity after proper stimulation in vitro and that such property is negatively regulated by Ia-positive cells.
我们在此表明,刀豆球蛋白A(Con A)、佛波酯(PMA)和离子霉素(Iono)的组合可重复性地刺激无胸腺裸鼠(Nu/Nu)的脾细胞以及正常和无胸腺裸鼠的骨髓细胞在体外分泌白细胞介素3(IL-3)。通过其支持已知仅在IL-3中生长的四种不同克隆生长的特性来测量IL-3。上述任何一种试剂以及测试的其他几种类型的刺激均不能诱导细胞分泌IL-3活性。培养24小时后可检测到两种组织诱导细胞中的IL-3活性,在48小时达到峰值,然后在培养72 - 96小时(骨髓细胞)时下降,或者在4天培养期内保持相对恒定(脾细胞)。参与无胸腺裸鼠脾脏中IL-3活性产生的细胞为THY1 +、L3T4 -、LyT2 -、B - 220 -、J11d -、Ia -,而正常或无胸腺裸鼠骨髓中的细胞为THY1 +、J11d +、L3T4 -、LyT2 -、B - 220 -、Ia -。最后,我们提供证据表明Ia阳性细胞对脾细胞和骨髓细胞产生IL-3活性具有负调节作用。我们得出结论,正常和无胸腺裸鼠的无胸腺裸鼠脾细胞和骨髓细胞在体外经过适当刺激后可分泌IL-3活性,且这种特性受到Ia阳性细胞的负调节。