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SPTAN1/NUMB axis senses cell density to restrain cell growth and oncogenesis through Hippo signaling
Dongxue Su, … , Lanfen Chen, Dawang Zhou
Dongxue Su, … , Lanfen Chen, Dawang Zhou
Published October 16, 2023
Citation Information: J Clin Invest. 2023;133(20):e168888. https://doi.org/10.1172/JCI168888.
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Research Article Cell biology Oncology

SPTAN1/NUMB axis senses cell density to restrain cell growth and oncogenesis through Hippo signaling

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Abstract

The loss of contact inhibition is a key step during carcinogenesis. The Hippo–Yes-associated protein (Hippo/YAP) pathway is an important regulator of cell growth in a cell density–dependent manner. However, how Hippo signaling senses cell density in this context remains elusive. Here, we report that high cell density induced the phosphorylation of spectrin α chain, nonerythrocytic 1 (SPTAN1), a plasma membrane–stabilizing protein, to recruit NUMB endocytic adaptor protein isoforms 1 and 2 (NUMB1/2), which further sequestered microtubule affinity–regulating kinases (MARKs) in the plasma membrane and rendered them inaccessible for phosphorylation and inhibition of the Hippo kinases sterile 20–like kinases MST1 and MST2 (MST1/2). WW45 interaction with MST1/2 was thereby enhanced, resulting in the activation of Hippo signaling to block YAP activity for cell contact inhibition. Importantly, low cell density led to SPTAN1 dephosphorylation and NUMB cytoplasmic location, along with MST1/2 inhibition and, consequently, YAP activation. Moreover, double KO of NUMB and WW45 in the liver led to appreciable organ enlargement and rapid tumorigenesis. Interestingly, NUMB isoforms 3 and 4, which have a truncated phosphotyrosine-binding (PTB) domain and are thus unable to interact with phosphorylated SPTAN1 and activate MST1/2, were selectively upregulated in liver cancer, which correlated with YAP activation. We have thus revealed a SPTAN1/NUMB1/2 axis that acts as a cell density sensor to restrain cell growth and oncogenesis by coupling external cell-cell contact signals to intracellular Hippo signaling.

Authors

Dongxue Su, Yuxi Li, Weiji Zhang, Huan Gao, Yao Cheng, Yongqiang Hou, Junhong Li, Yi Ye, Zhangjian Lai, Zhe Li, Haitao Huang, Jiaxin Li, Jinhuan Li, Mengyu Cheng, Cheng Nian, Na Wu, Zhien Zhou, Yunzhi Xing, Yu Zhao, He Liu, Jiayu Tang, Qinghua Chen, Lixin Hong, Wengang Li, Zhihai Peng, Bin Zhao, Randy L. Johnson, Pingguo Liu, Wanjin Hong, Lanfen Chen, Dawang Zhou

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Figure 3

SPTAN1 is required for NUMB1/2 membrane retention at HCD.

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SPTAN1 is required for NUMB1/2 membrane retention at HCD.
(A) Immunofluo...
(A) Immunofluorescence staining for NUMB (red) and DAPI (blue) in HepG2 cells transfected with the indicated siRNAs and cultured at HCD. Scale bars: 20 μm. (B) Immunoblot analysis of NUMB, SPTAN1, and GAPDH in HepG2 cells transfected with the indicated siRNAs. (C) Immunofluorescence staining for NUMB (green) and SPTAN1 (red) in WT and SPTAN1-KO HepG2 cells cultured at LCD or HCD. Scale bars: 20 μm. (D) Immunoblot analysis of SPTAN1 in the cytoplasmic fraction and the plasma membrane fraction, isolated from HepG2 cells cultured at LCD or HCD.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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