Apoptosis Department and Center for Genotoxic Stress Research, Institute of Cancer Biology, Danish Cancer Society, Copenhagen, Denmark.
Autophagy. 2011 Sep;7(9):1069-70. doi: 10.4161/auto.7.9.15886. Epub 2011 Sep 1.
The regulated lysosomal degradation pathway of autophagy prevents cellular damage and thus protects from malignant transformation. Autophagy is also required for the maturation of various hematopoietic lineages, namely the erythroid and lymphoid ones, yet its role in adult hematopoietic stem cells (HSCs) remained unexplored. While normal HSCs sustain life-long hematopoiesis, malignant transformation of HSCs or early progenitors leads to leukemia. Mechanisms protecting HSCs from cellular damage are therefore essential to prevent hematopoietic malignancies. By conditionally deleting the essential autophagy gene Atg7 in the hematopoietic system, we found that autophagy is required for the maintenance of true HSCs and therefore also of downstream hematopoietic progenitors. Loss of autophagy in HSCs leads to the expansion of a progenitor cell population in the bone marrow, giving rise to a severe, invasive myeloproliferation, which strongly resembles human acute myeloid leukemia (AML).
调控的溶酶体降解途径的自噬可以防止细胞损伤,从而防止恶性转化。自噬对于各种造血谱系的成熟也是必需的,即红细胞和淋巴细胞谱系,但它在成体造血干细胞(HSCs)中的作用仍未被探索。虽然正常的 HSCs 维持终身造血,但 HSCs 或早期祖细胞的恶性转化会导致白血病。因此,保护 HSCs 免受细胞损伤的机制对于预防造血系统恶性肿瘤至关重要。通过在造血系统中条件性地删除必需的自噬基因 Atg7,我们发现自噬对于真正的 HSCs 的维持以及下游造血祖细胞的维持是必需的。HSCs 中的自噬缺失会导致骨髓中祖细胞群体的扩张,从而导致严重的侵袭性骨髓增生,这非常类似于人类急性髓细胞白血病(AML)。