Park Joung-Sun, Kim Young-Shin, Yoo Mi-Ae
Department of Molecular Biology, Pusan National University, Busan 609-735, Korea.
Aging (Albany NY). 2009 May 21;1(7):637-51. doi: 10.18632/aging.100054.
It is important to understand how age-related changes in intestinal stem cells (ISCs) may contribute to age-associated intestinal diseases, including cancer. Drosophila midgut is an excellent model system for the study of ISC proliferation and differentiation. Recently, age-related changes in the Drosophila midgut have been shown to include an increase in ISC proliferation and accumulation of mis-differentiated ISC daughter cells. Here, we show that the p38b MAPK pathway contributes to the age-related changes in ISC and progenitor cells in Drosophila. D-p38b MAPK is required for an age-related increase of ISC proliferation. In addition, this pathway is involved in age and oxidative stress-associated mis-differentiation of enterocytes and upregulation of Delta, a Notch receptor ligand. Furthermore, we also show that D-p38b acts downstream of PVF2/PVR signaling in these age-related changes. Taken together, our findings suggest that p38 MAPK plays a crucial role in the balance between ISC proliferation and proper differentiation in the adult Drosophila midgut.
了解肠道干细胞(ISC)中与年龄相关的变化如何导致包括癌症在内的与年龄相关的肠道疾病至关重要。果蝇中肠是研究ISC增殖和分化的优秀模型系统。最近,已表明果蝇中肠与年龄相关的变化包括ISC增殖增加和错分化的ISC子代细胞积累。在这里,我们表明p38b MAPK通路促成了果蝇中ISC和祖细胞与年龄相关的变化。D-p38b MAPK是ISC增殖与年龄相关增加所必需的。此外,该通路参与了与年龄和氧化应激相关的肠上皮细胞错分化以及Notch受体配体Delta的上调。此外,我们还表明D-p38b在这些与年龄相关的变化中位于PVF2/PVR信号传导的下游。综上所述,我们的研究结果表明p38 MAPK在成年果蝇中肠的ISC增殖和正常分化之间的平衡中起关键作用。