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KAP1 Phosphorylation Promotes the Survival of Neural Stem Cells After Ischemia/reperfusion by Maintaining the Stability of PCNA

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Publisher Biomed Central
Date 2022 Jul 7
PMID 35799276
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Abstract

Aims: To explore the function of phosphorylation of KAP1 (p-KAP1) at the serine-824 site (S824) in the proliferation and apoptosis of endogenous neural stem cells (NSCs) after cerebral ischemic/reperfusion (I/R).

Methods: The apoptosis and proliferation of C17.2 cells transfected with the p-KAP1-expression plasmids and the expression of proliferation cell nuclear antigen (PCNA) and p-KAP1 were detected by immunofluorescence and Western blotting after the Oxygen Glucose deprivation/reperfusion model (OGD/R). The interaction of p-KAP1 and CUL4A with PCNA was analyzed by immunoprecipitation. In the rats MCAO model, we performed the adeno-associated virus (AAV) 2/9 gene delivery of p-KAP1 mutants to verify the proliferation of endogenous NSCs and the colocalization of PCNA and CUL4A by immunofluorescence.

Results: The level of p-KAP1 was significantly down-regulated in the stroke model in vivo and in vitro. Simulated p-KAP1(S824) significantly increased the proliferation of C17.2 cells and the expression of PCNA after OGD/R. Simulated p-KAP1(S824) enhanced the binding of p-KAP1 and PCNA and decreased the interaction between PCNA and CUL4A in C17.2 cells subjected to OGD/R. The AAV2/9-mediated p-KAP1(S824) increased endogenous NSCs proliferation, PCNA expression, p-KAP1 binding to PCNA, and improved neurological function in the rat MCAO model.

Conclusions: Our findings confirmed that simulated p-KAP1(S824) improved the survival and proliferation of endogenous NSCs. The underlying mechanism is that highly expressed p-KAP1(S824) promotes binding to PCNA, and inhibits the binding of CUL4A to PCNA. This reduced CUL4A-mediated ubiquitination degradation to increase the stability of PCNA and promote the survival and proliferation of NSCs.

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References
1.
Al-Hakim A, Escribano-Diaz C, Landry M, ODonnell L, Panier S, Szilard R . The ubiquitous role of ubiquitin in the DNA damage response. DNA Repair (Amst). 2010; 9(12):1229-40. PMC: 7105183. DOI: 10.1016/j.dnarep.2010.09.011. View

2.
Pilzecker B, Buoninfante O, van den Berk P, Lancini C, Song J, Citterio E . DNA damage tolerance in hematopoietic stem and progenitor cells in mice. Proc Natl Acad Sci U S A. 2017; 114(33):E6875-E6883. PMC: 5565453. DOI: 10.1073/pnas.1706508114. View

3.
Liao L, Lau B, Sanchez-Vidana D, Gao Q . Exogenous neural stem cell transplantation for cerebral ischemia. Neural Regen Res. 2019; 14(7):1129-1137. PMC: 6425845. DOI: 10.4103/1673-5374.251188. View

4.
Zhao H, Lo Y, Ma L, Waltz S, Gray J, Hung M . Targeting tyrosine phosphorylation of PCNA inhibits prostate cancer growth. Mol Cancer Ther. 2011; 10(1):29-36. PMC: 3066081. DOI: 10.1158/1535-7163.MCT-10-0778. View

5.
Zuilkoski C, Skibbens R . PCNA antagonizes cohesin-dependent roles in genomic stability. PLoS One. 2020; 15(10):e0235103. PMC: 7571713. DOI: 10.1371/journal.pone.0235103. View