TIMAP, a Regulatory Subunit of Protein Phosphatase 1, Inhibits In Vitro Neuronal Differentiation

被引:2
作者
Fonodi, Marton [1 ]
Thalwieser, Zsofia [1 ]
Csortos, Csilla [1 ]
Boratko, Anita [1 ]
机构
[1] Univ Debrecen, Fac Med, Dept Med Chem, Egyet Ter 1, H-4032 Debrecen, Hungary
关键词
TIMAP; protein phosphatase; neuroblastoma; differentiation; interactome; PHEOCHROMOCYTOMA PC12 CELLS; HUMAN NEUROBLASTOMA-CELLS; TRANS-RETINOIC ACID; NEURITE OUTGROWTH; SH-SY5Y CELLS; EXPRESSION; MODEL; PHOSPHORYLATION; ISOFORMS; GROWTH;
D O I
10.3390/ijms242417360
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
TIMAP (TGF-beta-inhibited membrane associated protein) is abundant in endothelial cells, and it has been regarded as a member of the myosin phosphatase targeting protein (MYPT) family. Our workgroup previously identified several interacting protein partners of TIMAP and proved its regulatory subunit role for protein phosphatase 1 catalytic subunit (PP1c). TIMAP is also expressed in neuronal cells, but details of its function have not been studied yet. Therefore, we aimed to explore the role of TIMAP in neuronal cells, especially during differentiation. Expression of TIMAP was proved both at mRNA and protein levels in SH-SY5Y human neuroblastoma cells. Differentiation of SH-SY5Y cells was optimized and proved by the detection of neuronal differentiation markers, such as beta 3-tubulin, nestin and inhibitor of differentiation 1 (ID1) using qPCR and Western blot. We found downregulation of TIMAP during differentiation. In accordance with this, overexpression of recombinant TIMAP attenuated the differentiation of neuronal cells. Moreover, the subcellular localization of TIMAP has changed during differentiation as it translocated from the plasma membrane into the nucleus. The nuclear interactome of TIMAP revealed more than 50 proteins, offering the possibility to further investigate the role of TIMAP in several key physiological pathways of neuronal cells.
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页数:17
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