Fabry M E, Suzuka S M, Weinberg R S, Lawrence C, Factor S M, Gilman J G, Costantini F, Nagel R L
Departments of Medicine and Pathology, Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NY 10461, USA.
Blood. 2001 Jan 15;97(2):410-8. doi: 10.1182/blood.v97.2.410.
Sickle transgenic mice expressing exclusively human globins are desirable for studying pathophysiology and testing gene therapy strategies, but they must have significant pathology and show evidence of amelioration by antisickling hemoglobins. Mice were generated that expressed exclusively human sickle hemoglobin with 3 levels of HbF using their previously described sickle constructs (cointegrated human miniLCRalpha2 and miniLCRbeta(S) [PNAS 89:12150, 1992]), mouse alpha- and beta-globin-knockouts, and 3 different human gamma-transgenes. It was found that, at all 3 levels of HbF expression, these mice have balanced chain synthesis, nearly normal mean corpuscular hemoglobin, and, in some cases, F cells. Mice with the least adult HbF expression were the most severe. Progressive increase in HbF from less than 3% to 20% to 40% correlated with progressive increase in hematocrit (22% to 34% to 40%) and progressive decrease in reticulocyte count (from 60% to 30% to 13%). Urine concentrating ability was normalized at high HbF, and tissue damage detected by histopathology and organ weight were ameliorated by increased HbF. The gamma-transgene that produces intermediate levels of HbF was introduced into knockout sickle mice described by Pàszty and coworkers that express the miniLCRalpha1(G)gamma(A)gammadeltabeta(S) transgene and have fetal but not adult expression of HbF. It was found that the level of HbF required to ameliorate low hematocrit and normalize urine concentrating defect was different for the miniLCRalpha2beta(S) and miniLCRalpha1(G)gamma(A)gammadeltabeta(S) mice. We conclude that knockout mice with the miniLCRalpha2beta(S) transgene and postnatal expression of HbF have sufficiently faithful sickle pathology to serve as a platform for testing antisickling interventions.
表达纯人类珠蛋白的镰状转基因小鼠对于研究病理生理学和测试基因治疗策略是很有必要的,但它们必须有明显的病理学表现,并显示出抗镰状血红蛋白改善病情的证据。利用他们之前描述的镰状构建体(共整合人类微型LCRα2和微型LCRβ(S) [《美国国家科学院院刊》89:12150, 1992])、小鼠α和β珠蛋白基因敲除以及3种不同的人类γ转基因,培育出了只表达人类镰状血红蛋白且有3种HbF水平的小鼠。研究发现,在所有3种HbF表达水平下,这些小鼠的链合成平衡,平均红细胞血红蛋白接近正常,在某些情况下还有F细胞。成年HbF表达最少的小鼠病情最严重。HbF从低于3%逐渐增加到20%再到40%,与血细胞比容逐渐增加(从22%到34%再到40%)以及网织红细胞计数逐渐减少(从60%到30%再到13%)相关。高HbF水平时尿液浓缩能力恢复正常,组织病理学和器官重量检测到的组织损伤也因HbF增加而改善。将产生中等水平HbF的γ转基因导入由帕斯蒂及其同事描述的基因敲除镰状小鼠中,这些小鼠表达微型LCRα1(G)γ(A)γδβ(S)转基因,HbF只有胎儿期表达而无成年期表达。研究发现,对于微型LCRα2β(S)和微型LCRα1(G)γ(A)γδβ(S)小鼠,改善低血细胞比容和使尿液浓缩缺陷恢复正常所需的HbF水平不同。我们得出结论,带有微型LCRα2β(S)转基因且HbF有出生后表达的基因敲除小鼠有足够逼真的镰状病理表现,可作为测试抗镰状干预措施的平台。