Golgi-to-ER retrograde transport prevents premature differentiation of Drosophila type II neuroblasts via Notch-signal-sending daughter cells.

Golgi-to-ER retrograde transport prevents premature differentiation of Drosophila type II neuroblasts via Notch-signal-sending daughter cells.
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DOI:
10.1016/j.isci.2023.108545
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发表时间:
2024-01-19
期刊:
影响因子:
5.8
通讯作者:
Wang, Su
Wang, Su
中科院分区:
综合性期刊2区
文献类型:
--
作者:
Zhang, Huanhuan;Rui, Menglong;Ma, Zhixin;Gong, Sifan;Zhang, Shuliu;Zhou, Qingxia;Gan, Congfeng;Gong, Wenting;Wang, Su

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Stem cells are heterogeneous to generate diverse differentiated cell types required for organogenesis; however, the underlying mechanisms that differently maintain these heterogeneous stem cells are not well understood. In this study, we identify that Golgi-to-endoplasmic reticulum (ER) retrograde transport specifically maintains type II neuroblasts (NBs) through the Notch signaling. We reveal that intermediate neural progenitors (INPs), immediate daughter cells of type II NBs, provide Delta and function as the NB niche. The Delta used by INPs is mainly produced by NBs and asymmetrically distributed to INPs. Blocking retrograde transport leads to a decrease in INP number, which reduces Notch activity and results in the premature differentiation of type II NBs. Furthermore, the reduction of Delta could suppress tumor formation caused by type II NBs. Our results highlight the crosstalk between Golgi-to-ER retrograde transport, Notch signaling, stem cell niche, and fusion as an essential step in maintaining the self-renewal of type II NB lineage. Blocking RT specifically affects type II NBs by reducing Notch activity INPs provide Delta to NBs as niche The Delta generated by type II NBs was asymmetrically distributed into INPs Biological sciences; Microbiology; Cell biology
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