Burstein S A, Adamson J W, Erb S K, Harker L A
J Cell Physiol. 1981 Nov;109(2):333-41. doi: 10.1002/jcp.1041090217.
The response of murine megakaryocytopoiesis was studied under conditions of varying platelet demand. Twenty-four hours after mice were given a single injection of rabbit anti-platelet serum, megakaryocyte number and volume were increased, becoming maximal at 65 and 40 hr, respectively. Total body megakaryocytic colony-forming unit (CFU-M) numbers did not change until 90 hr, when a 35% increase in the experimental group was noted. The percentage of CFU-M in DNA synthesis in the experimental group was 38 +/-2% at 24 hr, 49 +/- 1% at 40 hr, and returned to normal (11 +/- 3%) at 90 hr. When mice were made thrombocytotic by platelet transfusions, both megakaryocyte number and volume were decreased compared to controls, while no difference was noted in the number and percentage of CFU-M in DNA synthesis. Finally, experiments were performed to examine the effect of platelet transfusions on regenerating marrow. Experimental mice were given platelet transfusions while control animals received platelet buffer solution. At sacrifice the number and volume of megakaryocytes in the experimental group (platelet count 2.568 X 10(6)/microliters) were less than controls (platelet count 0.363 X 10(6)/microliters), while the number and percentage of CFU-M in DNA synthesis were similar in both groups. These results demonstrate that CFU-M are not immediately responsive to acute changes in platelet demand. The data suggest that megakaryocytopoiesis is structured on at least two levels which are independently regulated.
在不同血小板需求条件下研究了小鼠巨核细胞生成情况。给小鼠单次注射兔抗血小板血清24小时后,巨核细胞数量和体积增加,分别在65小时和40小时达到最大值。全身巨核细胞集落形成单位(CFU-M)数量直到90小时才发生变化,此时实验组增加了35%。实验组中处于DNA合成期的CFU-M百分比在24小时时为38±2%,40小时时为49±1%,90小时时恢复正常(11±3%)。当通过输注血小板使小鼠血小板增多时,与对照组相比,巨核细胞数量和体积均减少,而处于DNA合成期的CFU-M数量和百分比没有差异。最后,进行实验以研究输注血小板对再生骨髓的影响。给实验小鼠输注血小板,而对照动物输注血小板缓冲液。处死时,实验组(血小板计数2.568×10⁶/微升)的巨核细胞数量和体积少于对照组(血小板计数0.363×10⁶/微升),而两组中处于DNA合成期的CFU-M数量和百分比相似。这些结果表明,CFU-M对血小板需求的急性变化没有立即反应。数据表明,巨核细胞生成至少在两个独立调节的水平上构建。