Author
Listed:
- Yuuki Obata
(Research Institute for Biomedical Sciences, Tokyo University of Science)
- Shota Toyoshima
(Research Institute for Biomedical Sciences, Tokyo University of Science)
- Ei Wakamatsu
(Research Institute for Biomedical Sciences, Tokyo University of Science)
- Shunichi Suzuki
(Research Institute for Biomedical Sciences, Tokyo University of Science)
- Shuhei Ogawa
(Research Institute for Biomedical Sciences, Tokyo University of Science)
- Hiroyasu Esumi
(Research Institute for Biomedical Sciences, Tokyo University of Science
National Cancer Center Hospital East)
- Ryo Abe
(Research Institute for Biomedical Sciences, Tokyo University of Science)
Abstract
Kit is a receptor-type tyrosine kinase found on the plasma membrane. It can transform mast cells through activating mutations. Here, we show that a mutant Kit from neoplastic mast cells from mice, Kit(D814Y), is permanently active and allows cells to proliferate autonomously. It does so by activating two signalling pathways from different intracellular compartments. Mutant Kit from the cell surface accumulates on endolysosomes through clathrin-mediated endocytosis, which requires Kit’s kinase activity. Kit(D814Y) is constitutively associated with phosphatidylinositol 3-kinase, but the complex activates Akt only on the cytoplasmic surface of endolysosomes. It resists destruction because it is under-ubiquitinated. Kit(D814Y) also appears in the endoplasmic reticulum soon after biosynthesis, and there, can activate STAT5 aberrantly. These mechanisms of oncogenic signalling are also seen in rat and human mast cell leukemia cells. Thus, oncogenic Kit signalling occurs from different intracellular compartments, and the mutation acts by altering Kit trafficking as well as activation.
Suggested Citation
Yuuki Obata & Shota Toyoshima & Ei Wakamatsu & Shunichi Suzuki & Shuhei Ogawa & Hiroyasu Esumi & Ryo Abe, 2014.
"Oncogenic Kit signals on endolysosomes and endoplasmic reticulum are essential for neoplastic mast cell proliferation,"
Nature Communications, Nature, vol. 5(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6715
DOI: 10.1038/ncomms6715
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