Adler S S, Trobauch F E, Knospe W H
J Lab Clin Med. 1977 Mar;89(3):592-602.
89Sr was used to ablate the marrows of 12- to 16-week-old CAF1 mice. The CFU-S of their blood, marrows, and spleens were assayed at intervals from days 10 through 56. The effects of splenectomy performed on day 14 or 42 on the numbers of CFU-S in the blood and marrow were also studied. On day 10 after treatment with 89Sr both the cellularity and CFU-S of the marrow were markedly decreased. Later, especially during the third week after treatment, marrow cellularity increased and by day 56 had returned to 74 percent of normal; the concentration of marrow CFU-S also increased but by day 56 had attained a level of only one-third normal. Thus, replenishment of the marrow's CFU-S lagged behind the repletion of its cellularity. Spleen and blood CFU-S were elevated throughout the 56 days. The number of splenic CFU-S was highest at day 10, decreased somewhat by day 21, and remained remarkably stable thereafter. After splenectomy there was a significant decline in the content of both blood and marrow CFU-S, whereas the reverse occurred in the "cold" 88Sr-treated control group. The results of these studies suggest that in the 89Sr-irradiated animal the spleen is transformed from a trapper to the prime supplier of CFU-S and that in normal mice the spleen may suppress marrow CFU-S proliferation. An inverse relationship between the size of the pool of mature granulocytes and the number of CFU-S was found, suggesting that the granulocyte compartment may, at least in part, play a role in the regulation of CFU-S proliferation.
用89Sr对12至16周龄的CAF1小鼠进行骨髓消融。在第10天至56天期间,定期检测其血液、骨髓和脾脏中的脾集落形成单位(CFU-S)。还研究了在第14天或第42天进行脾切除对血液和骨髓中CFU-S数量的影响。用89Sr治疗后第10天,骨髓的细胞数量和CFU-S均显著减少。随后,尤其是在治疗后的第三周,骨髓细胞数量增加,到第56天时已恢复到正常水平的74%;骨髓CFU-S的浓度也有所增加,但到第56天时仅达到正常水平的三分之一。因此,骨髓CFU-S的补充落后于其细胞数量的恢复。在整个56天内,脾脏和血液中的CFU-S均升高。脾脏CFU-S的数量在第10天最高,到第21天有所下降,此后保持相当稳定。脾切除后,血液和骨髓中CFU-S的含量均显著下降,而在“冷”88Sr处理的对照组中则出现相反情况。这些研究结果表明,在89Sr照射的动物中,脾脏从CFU-S的捕获器官转变为主要供应器官,并且在正常小鼠中,脾脏可能抑制骨髓CFU-S的增殖。发现成熟粒细胞池的大小与CFU-S的数量呈负相关,这表明粒细胞部分至少在一定程度上可能参与CFU-S增殖的调节。