State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China
FASEB J. 2014 Jul;28(7):2816-27. doi: 10.1096/fj.13-244632. Epub 2014 Mar 25.
iASPP is a member of the apoptosis-stimulating proteins of p53 (ASPP) family and negatively regulates the apoptotic function of p53. In a hematopoietic system, overexpression of iASPP results in blockage of apoptosis, which may play a role in regulating hematopoietic stem cell (HSC) numbers. To address this, we first analyzed the expression of iASPP in patients with acute leukemia (AL) and found it was highly expressed in patients with AL. We further established a transgenic mouse model in which human iASPP was specifically expressed in hematopoietic cells. Overexpression of iASPP led to an increase in the proportion of long-term HSCs, short-term HSCs, multipotent progenitors, and common myeloid progenitor. HSCs from iASPP transgenic mice had an advantage in long-term reconstitution potential. In addition, the hematopoietic cells from iASPP transgenic mice exhibited a significantly lower level of p53 dependent apoptosis. After irradiation damage, hematopoietic cells of iASPP transgenic mice had a higher level of γ-H2AX expression, which lasted for a longer time. These results provide the first evidence that the iASPP can increase HSC populations and reconstitution capacity. Interestingly, in response to cell damage stimuli, hematopoietic cells can be protected against apoptosis by iASPP; meanwhile these apoptosis-resistant cells would have more mutation accumulation, which might be the potential risk for malignant transformation.-Jia, Y., Peng, L., Rao, Q., Xing, H., Huai, L., Yu, P., Chen, Y., Wang, C., Wang, M., Mi, Y., Wang, J. Oncogene iASPP enhances self-renewal of hematopoietic stem cells and facilitates their resistance to chemotherapy and irradiation.
iASPP 是 p53(凋亡刺激蛋白)家族的成员,负向调节 p53 的凋亡功能。在造血系统中,iASPP 的过表达导致凋亡受阻,这可能在调节造血干细胞(HSC)数量方面发挥作用。为了解决这个问题,我们首先分析了急性白血病(AL)患者中 iASPP 的表达情况,发现其在 AL 患者中高表达。我们进一步建立了一种转基因小鼠模型,其中人 iASPP 特异性表达于造血细胞。iASPP 的过表达导致长期 HSC、短期 HSC、多能祖细胞和共同髓系祖细胞的比例增加。iASPP 转基因小鼠的 HSCs 具有长期重建潜能的优势。此外,iASPP 转基因小鼠的造血细胞表现出明显较低水平的 p53 依赖性凋亡。在照射损伤后,iASPP 转基因小鼠的造血细胞中γ-H2AX 的表达水平更高,持续时间更长。这些结果首次提供了证据表明 iASPP 可以增加 HSC 群体和重建能力。有趣的是,在应对细胞损伤刺激时,造血细胞可以通过 iASPP 来防止凋亡;同时,这些抗凋亡细胞会有更多的突变积累,这可能是恶性转化的潜在风险。-贾,Y.,彭,L.,饶,Q.,邢,H.,槐,L.,于,P.,陈,Y.,王,C.,王,M.,米,Y.,王,J.。癌基因 iASPP 增强造血干细胞的自我更新能力,并促进其对化疗和辐射的耐药性。