Stremmel C, Schuchert R, Schneider V, Weinberger T, Thaler R, Messerer D, Helmer S, Geissmann F, Frampton J, Massberg S, Schulz C
Medizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany.
Immunology Program, Memorial Sloan Kettering Cancer Center (MSKCC), New York, NY 10065, USA.
J Immunol Methods. 2018 Jun;457:66-72. doi: 10.1016/j.jim.2018.03.016. Epub 2018 Apr 6.
Allogeneic bone marrow (BM) transplantation enables the in vivo functional assessment of hematopoietic cells. As pre-conditioning, ionizing radiation is commonly applied to induce BM depletion, however, it exerts adverse effects on the animal and can limit experimental outcome. Here, we provide an alternative method that harnesses conditional gene deletion to ablate c-myb and thereby deplete BM cells, hence allowing BM substitution without other pre-conditioning. The protocol results in a high level of blood chimerism after allogeneic BM transplantation, whereas immune cells in peripheral tissues such as resident macrophages are not replaced. Further, mice featuring a low chimerism after initial transplantation can undergo a second induction cycle for efficient deletion of residual BM cells without the necessity to re-apply donor cells. In summary, we present an effective c-myb-dependent genetic technique to generate BM chimeras in the absence of irradiation or other methods for pre-conditioning.
异基因骨髓(BM)移植能够对造血细胞进行体内功能评估。作为预处理,通常采用电离辐射来诱导骨髓耗竭,然而,它会对动物产生不利影响并可能限制实验结果。在此,我们提供了一种替代方法,该方法利用条件性基因缺失来敲除c-myb,从而耗尽骨髓细胞,进而在无需其他预处理的情况下实现骨髓替代。该方案在异基因骨髓移植后可导致高水平的血液嵌合现象,而外周组织中的免疫细胞,如驻留巨噬细胞,则不会被替代。此外,初次移植后嵌合率较低的小鼠可经历第二个诱导周期,以有效清除残留的骨髓细胞,而无需重新输入供体细胞。总之,我们提出了一种有效的依赖c-myb的基因技术,可在无辐射或其他预处理方法的情况下生成骨髓嵌合体。