Leigh B R, Khan W, Hancock S L, Knox S J
Department of Radiation Oncology, Stanford University Hospital, California 94305.
Radiat Res. 1995 Apr;142(1):12-5.
Recombinant rat stem cell factor (SCF) has been shown to decrease lethality in mice exposed to total-body irradiation (TBI) in the lower range of lethality through radioprotection of hematopoietic stem cells and acceleration of bone marrow repopulation. This study evaluates the effect of SCF on the survival of the intestinal mucosal stem cell after TBI. This non-hematopoietic stem cell is clinically relevant. Gastrointestinal toxicity is common during and after abdominal and pelvic radiation therapy and limits the radiation dose in these regions. As observed with bone marrow, the administration of SCF to mice prior to TBI enhanced the survival of mouse duodenal crypt stem cells. The maximum enhancement of survival was seen when 100 micrograms/kg of SCF was given intraperitoneally 8 h before irradiation. This regimen increased the survival of duodenal crypt stem cells after 12.0 Gy TBI from 22.5 +/- 0.7 per duodenal cross section for controls to 30.0 +/- 1.7 after treatment with SCF (P = 0.03). The TBI dose producing 50% mortality at 6 days (LD50/6) was increased from 14.9 Gy for control mice to 19.0 Gy for mice treated with SCF (dose modification factor = 1.28). These findings demonstrate that SCF has radioprotective effects on a non-hematopoietic stem cell population and suggest that SCF may be of clinical value in preventing radiation injury to the intestine.
重组大鼠干细胞因子(SCF)已被证明,通过对造血干细胞的辐射防护和加速骨髓再增殖,可降低处于较低致死率范围内接受全身照射(TBI)的小鼠的死亡率。本研究评估了SCF对TBI后肠黏膜干细胞存活的影响。这种非造血干细胞具有临床相关性。胃肠道毒性在腹部和盆腔放射治疗期间及之后很常见,并限制了这些区域的放射剂量。正如在骨髓中观察到的那样,在TBI前给小鼠施用SCF可提高小鼠十二指肠隐窝干细胞的存活率。在照射前8小时腹腔注射100微克/千克的SCF时,观察到存活率的最大提高。该方案使12.0 Gy TBI后十二指肠隐窝干细胞的存活率从对照组每十二指肠横截面积22.5±0.7增加到SCF治疗后的30.0±1.7(P = 0.03)。在6天产生50%死亡率的TBI剂量(LD50/6)从对照小鼠的14.9 Gy增加到用SCF治疗的小鼠的19.0 Gy(剂量修正因子 = 1.28)。这些发现表明,SCF对非造血干细胞群体具有辐射防护作用,并提示SCF在预防肠道辐射损伤方面可能具有临床价值。