Iwasaki T, Hamano T, Saheki K, Kuroiwa T, Kataoka Y, Takemoto Y, Ogata A, Sugihara A, Terada N, Fujimoto J, Kakishita E
Second Department of Internal Medicine, First Department of Pathology, First Department of Surgery, Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo, 663-8501, Japan.
Cell Immunol. 1999 Oct 10;197(1):30-8. doi: 10.1006/cimm.1999.1553.
The acute graft-versus-host disease (GVHD) generated in BDF1 mice by the injection of spleen cells from the C57BL/6 parental strain induces a direct cell-mediated attack on host lymphohematopoietic populations, resulting in the reconstitution of the host with donor hematopoietic stem cells. We examined the effect of GVHD on the donor and host hematopoiesis in parental-induced acute GVHD. The bone marrow was hypoplastic and the number of hematopoietic progenitor cells significantly decreased at 4 weeks after GVHD induction. However, extramedullary splenic hematopoiesis was present and the number of hematopoietic progenitor cells in the spleen significantly increased at this time. Fas expression on the host spleen cells and bone marrow cells significantly increased during weeks 2 to 8 of GVHD. Host cell incubation with anti-Fas Ab induced apoptosis, and the number of hematopoietic progenitor cells decreased during these weeks. A significant correlation between the augmented Fas expression on host bone marrow cells and the decreased number of host bone marrow cells by acute GVHD was observed. Furthermore, the injection of Fas ligand (FasL)-deficient B6/gld spleen cells failed to affect host bone marrow cells. Although Fas expression on repopulating donor cells also increased, Fas-induced apoptosis by the repopulating donor cells was not remarkable until 12 weeks, when more than 90% of the cells were donor cells. The number of hematopoietic progenitor cells in the bone marrow and the spleen by the repopulating donor cells, however, decreased over an extended time during acute GVHD. This suggests that Fas-FasL interactions may regulate suppression of host hematopoietic cells but not of donor hematopoietic cells. Hematopoietic dysfunctions caused by the reconstituted donor cells are independent to Fas-FasL interactions and persisted for a long time during parental-induced acute GVHD.
通过注射C57BL/6亲本品系的脾细胞在BDF1小鼠中产生的急性移植物抗宿主病(GVHD)会引发对宿主淋巴造血群体的直接细胞介导攻击,从而导致宿主由供体造血干细胞进行重建。我们研究了亲本品系诱导的急性GVHD中GVHD对供体和宿主造血的影响。GVHD诱导后4周,骨髓发育不全,造血祖细胞数量显著减少。然而,此时存在脾外造血,脾脏中的造血祖细胞数量显著增加。在GVHD的第2至8周期间,宿主脾细胞和骨髓细胞上的Fas表达显著增加。用抗Fas抗体孵育宿主细胞可诱导细胞凋亡,并且在这些周期间造血祖细胞数量减少。观察到急性GVHD导致宿主骨髓细胞上Fas表达增加与宿主骨髓细胞数量减少之间存在显著相关性。此外,注射Fas配体(FasL)缺陷的B6/gld脾细胞对宿主骨髓细胞没有影响。尽管再植供体细胞上的Fas表达也增加,但直到12周时,当超过90%的细胞为供体细胞时,再植供体细胞通过Fas诱导的细胞凋亡才较为明显。然而,在急性GVHD期间,再植供体细胞在骨髓和脾脏中的造血祖细胞数量在较长时间内持续减少。这表明Fas - FasL相互作用可能调节对宿主造血细胞的抑制,但不调节对供体造血细胞的抑制。由再植供体细胞引起的造血功能障碍独立于Fas - FasL相互作用,并且在亲本品系诱导的急性GVHD期间持续很长时间。