Laterveer L, Lindley I J, Hamilton M S, Willemze R, Fibbe W E
Department of Hematology, University Medical Center Leiden, The Netherlands.
Blood. 1995 Apr 15;85(8):2269-75.
Interleukin-8 (IL-8) belongs to a family of chemoattractant cytokines involved in chemotaxis and activation of neutrophils. As in vivo administration of IL-8 induces granulocytosis and the release of immature white blood cells into the circulation, we assessed a possible mobilizing effect of IL-8 on myeloid progenitor cells. IL-8 was administered at intraperitoneal doses ranging from 0.1 to 100 micrograms per mouse to female Balb/C mice (aged 8 to 12 weeks; weight, 20 to 25 g). Animals were killed at time intervals ranging from 1 to 240 minutes after IL-8 administration, and blood, bone marrow, and spleen cells were harvested. Injection of 30 micrograms IL-8 resulted in an increment from 25 +/- 9 to 418 +/- 299 granulocyte-macrophage colony-forming units (CFU-GM) per milliliter blood at 15 minutes after a single intraperitoneal injection. Sixty minutes after the injection of IL-8, the numbers of circulating CFU-GM per milliliter blood had almost returned to pretreatment values (82 +/- 39 CFU-GM per milliliter). A dose of 100 micrograms IL-8 per animal did not result in a further increment in the number of circulating CFU-GM. Transplantation of 5 x 10(5) blood-derived mononuclear cells (MNC) obtained at 30 minutes after IL-8 injection (30 micrograms) resulted in 69% survival of lethally irradiated (8.5 Gy) recipients at 60 days versus 22% for animals transplanted with an equal number of nonprimed blood-derived MNC. Transplantation of 1.5 x 10(6) MNC obtained from IL-8-treated donors resulted in 100% survival. Six months after transplantation, female recipients of MNC derived from IL-8-treated male donors were killed, and chimerism was determined in bone marrow, spleen, and thymus using a Y chromosome-specific probe and fluorescent in situ hybridization (FISH). The majority of bone marrow, spleen, and thymus cells (83% +/- 25%, 89% +/- 5%, and 64 +/- 28%, respectively) consisted of Y chromosome-positive cells, showing that the IL-8-mobilized cells had myelolymphoid repopulating ability. We conclude that IL-8 is a cytokine that induces rapid mobilization of progenitor cells and pluripotent stem cells that are able to rescue lethally irradiated mice and that are able to completely and permanently repopulate host hematopoietic tissues.
白细胞介素-8(IL-8)属于趋化因子细胞因子家族,参与中性粒细胞的趋化作用和激活。由于在体内给予IL-8会诱导粒细胞增多症,并使未成熟白细胞释放到循环中,我们评估了IL-8对髓系祖细胞的可能动员作用。以每只小鼠0.1至100微克的腹腔注射剂量向雌性Balb/C小鼠(8至12周龄;体重20至25克)给予IL-8。在给予IL-8后的1至240分钟的时间间隔处死动物,并采集血液、骨髓和脾细胞。单次腹腔注射后15分钟,注射30微克IL-8导致每毫升血液中的粒细胞-巨噬细胞集落形成单位(CFU-GM)从25±9增加到418±299。注射IL-8后60分钟,每毫升血液中循环的CFU-GM数量几乎恢复到预处理值(每毫升82±39 CFU-GM)。每只动物给予100微克IL-8的剂量并未导致循环CFU-GM数量的进一步增加。移植在注射IL-8(30微克)后30分钟获得的5×10⁵个血液来源的单核细胞(MNC),导致接受致死性照射(8.5 Gy)的受体在60天时的存活率为69%,而移植等量未预处理血液来源MNC的动物存活率为22%。移植从经IL-8处理的供体获得的1.5×10⁶个MNC导致100%的存活率。移植后6个月,处死来自经IL-8处理的雄性供体的MNC的雌性受体,并使用Y染色体特异性探针和荧光原位杂交(FISH)在骨髓、脾脏和胸腺中测定嵌合情况。大多数骨髓、脾脏和胸腺细胞(分别为83%±25%、89%±5%和64±28%)由Y染色体阳性细胞组成,表明经IL-8动员的细胞具有骨髓淋巴系重建能力。我们得出结论,IL-8是一种细胞因子,可诱导祖细胞和多能干细胞的快速动员,这些细胞能够挽救接受致死性照射的小鼠,并能够完全且永久地重建宿主造血组织。