Repetitive magnetic stimulation promotes neural stem cells proliferation by upregulating MiR-106b in vitro

Hua Liu , Xiao-hua Han , Hong Chen , Cai-xia Zheng , Yi Yang , Xiao-lin Huang

Current Medical Science ›› 2015, Vol. 35 ›› Issue (5) : 766 -772.

PDF
Current Medical Science ›› 2015, Vol. 35 ›› Issue (5) : 766 -772. DOI: 10.1007/s11596-015-1505-3
Article

Repetitive magnetic stimulation promotes neural stem cells proliferation by upregulating MiR-106b in vitro

Author information +
History +
PDF

Abstract

Neural stem cells (NSCs) proliferation can be influenced by repetitive transcranial magnetic stimulation (rTMS) in vivo via microRNA-106b-25 cluster, but the underlying mechanisms are poorly understood. This study investigated the involvement of microRNA-106b-25 cluster in the proliferation of NSCs after repetitive magnetic stimulation (rMS) in vitro. NSCs were stimulated by rMS (200/400/600/800/1000 pulses per day, with 10 Hz frequency and 50% maximum machine output) over a 3-day period. NSCs proliferation was detected by using ki-67 and EdU staining. Ki-67, p21, p57, cyclinD1, cyclinE, cyclinA, cdk2, cdk4 proteins and miR-106b, miR-93, miR-25 mRNAs were detected by Western blotting and qRT-PCR, respectively. The results showed that rMS could promote NSCs proliferation in a dose-dependent manner. The proportions of ki-67+ and Edu+ cells in 1000 pulses group were 20.65% and 4.00%, respectively, significantly higher than those in control group (9.25%, 2.05%). The expression levels of miR-106b and miR-93 were significantly upregulated in 600–1000 pulses groups compared with control group (P<0.05 or 0.01 for all). The expression levels of p21 protein were decreased significantly in 800/1000 pulses groups, and those of cyclinD1, cyclinA, cyclinE, cdk2 and cdk4 were obviously increased after rMS as compared with control group (P<0.05 or 0.01 for all). In conclusion, our findings suggested that rMS enhances the NSCs proliferation in vitro in a dose-dependent manner and miR-106b/p21/cdks/cyclins pathway was involved in the process.

Keywords

repetitive magnetic stimulation / neural stem cells / EdU / ki67 / microRNA-106b / cyclin-dependent kinase / cyclin-dependent kinase inhibitor

Cite this article

Download citation ▾
Hua Liu, Xiao-hua Han, Hong Chen, Cai-xia Zheng, Yi Yang, Xiao-lin Huang. Repetitive magnetic stimulation promotes neural stem cells proliferation by upregulating MiR-106b in vitro. Current Medical Science, 2015, 35(5): 766-772 DOI:10.1007/s11596-015-1505-3

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

PellGS, RothY, ZangenA. Modulation of cortical excitability induced by repetitive transcranial magnetic stimulation: influence of timing and geometrical parameters and underlying mechanisms. Prog Neurobiol, 2011, 93(1): 59-98 PMID: 21056619

[2]

TougeT, GerschlagerW, BrownP, et al. . Are the after- effects of low-frequency rTMS on motor cortex excitability due to changes in the efficacy of cortical synapses. Clin Neurophysiol, 2001, 112(11): 2138-2145 PMID: 11682353

[3]

BilekE, SchaferA, OchsE, et al. . Application of high-frequency repetitive transcranial magnetic stimulation to the DLPFC alters human prefrontal-hippocampal functional interaction. J Neurosci, 2013, 33(16): 7050-7056 PMID: 23595762

[4]

LisanbySH, DattoCJ, SzubaMP. ECT and TMS: past, present, and future. Depress Anxiety, 2000, 12(3): 115-117 PMID: 11126184

[5]

RothkegelH, SommerM, PaulusW. Breaks during 5Hz rTMS are essential for facilitatory after effects. Clin Neurophysiol, 2009, 121(3): 426-430 PMID: 20006546

[6]

PLoS One, 2014, 9(10

[7]

ZengY, YiR, CullenBR. Recognition and cleavage of primary microRNA precursors by the nuclear processing enzyme Drosha. EMBO J, 2005, 241): 138-148 PMCID: 544904 PMID: 15565168

[8]

SaitoK, IshizukaA, SiomiH, et al. . Processing of pre-microRNAs by the Dicer-1-Loquacious complex in Drosophila cells. PLoS Biol, 2005, 3(7): e235 PMCID: 1141268 PMID: 15918769

[9]

KimVN, HanJ, SiomiMC. Biogenesis of small RNAs in animals. Nat Rev Mol Cell Biol, 2009, 10(2): 126-139 PMID: 19165215

[10]

CremisiF. MicroRNAs and cell fate in cortical and retinal development. Front Cell Neurosci, 2013, 7: 141 PMCID: 3760135 PMID: 24027496

[11]

Perruisseau-CarrierC, JurgaM, ForrazN, et al. . miRNAs stem cell reprogramming for neuronal induction and differentiation. Mol Neurobiol, 2011, 43(3): 215-227 PMID: 21541853

[12]

ZhaoC, SunG, LiS, et al. . A feedback regulatory loop involving microRNA-9 and nuclear receptor TLX in neural stem cell fate determination. Nat Struct Mol Biol, 2009, 16(4): 365-371 PMCID: 2667220 PMID: 19330006

[13]

BrettJO, RenaultVM, RafalskiVA, et al. . The microRNA cluster miR-106b~25 regulates adult neural stem/progenitor cell proliferation and neuronal differentiation. Aging, 2011, 3(2): 108-124 PMCID: 3082007 PMID: 21386132

[14]

PeckB, SchulzeA. A role for the cancer-associated miR-106b~25 cluster in neuronal stem cells. Aging, 2011, 3(4): 329-331 PMCID: 3117442 PMID: 21483041

[15]

LandgrafP, RusuM, SheridanR, et al. . A mammalian microRNA expression atlas based on small RNA library sequencing. Cell, 2007, 129(7): 1401-1414 PMCID: 2681231 PMID: 17604727

[16]

MorteMI, CarreiraBP, MachadoV, et al. . Evaluation of proliferation of neural stem cells in vitro and in vivo. Curr Protoc Stem Cell Biol, 2013

[17]

LivakKJ, SchmittgenTD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods, 2001, 25(4): 402-408 PMID: 11846609

[18]

ContiL, CattaneoE. Neural stem cell systems: physiological players or in vitro entities. Nat Rev Neurosci, 2010, 11(3): 176-187 PMID: 20107441

[19]

SalicA, MitchisonTJ. A chemical method for fast and sensitive detection of DNA synthesis in vivo. Proc Natl Acad Sci U S A, 2008, 105(7): 2415-2420 PMCID: 2268151 PMID: 18272492

[20]

HayashiY, TakeiH, KurosumiM. Ki67 immunohistochemical staining: the present situation of diagnostic criteria. Nihon Rinsho, 2013, 70: 428-432

[21]

ReifA, FritzenS, FingerM, et al. . Neural stem cell proliferation is decreased in schizophrenia, but not in depression. Mol Psychiatry, 2006, 11(5): 514-522 PMID: 16415915

[22]

Arias-CarrionO, Verdugo-DiazL, Feria-VelascoA, et al. . Neurogenesis in the subventricular zone following transcranial magnetic field stimulation and nigrostriatal lesions. J Neurosci Res, 2004, 78(1): 16-28 PMID: 15372495

[23]

WernerS, UnsickerK, von Bohlen und HalbachO. Fibroblast growth factor-2 deficiency causes defects in adult hippocampal neurogenesis, which are not rescued by exogenous fibroblast growth factor-2. J Neurosci Res, 2011, 89(10): 1605-1617 PMID: 21800348

[24]

JeongCH, KimSM, LimJY, et al. . Mesenchymal stem cells expressing brain-derived neurotrophic factor enhance endogenous neurogenesis in an ischemic stroke model. Biomed Res Int, 2014, 2014: 129-145

[25]

EmsleyJG, HaggT. Endogenous and exogenous ciliary neurotrophic factor enhances forebrain neurogenesis in adult mice. Exp Neurol, 2003, 183(2): 298-310 PMID: 14552871

[26]

RotemA, MosesE. Magnetic stimulation of one-dimensional neuronal cultures. Biophys J, 2008, 94(12): 5065-5078 PMCID: 2397342 PMID: 18326634

[27]

KimJY, ChoiGS, ChoYW, et al. . Attenuation of spinal cord injury-induced astroglial and microglial activation by repetitive transcranial magnetic stimulation in rats. J Korean Med Sci, 2013, 28(2): 295-299 PMCID: 3565143 PMID: 23399872

[28]

UeyamaE, UkaiS, OgawaA, et al. . Chronic repetitive transcranial magnetic stimulation increases hippocampal neurogenesis in rats. Psychiatry Clin Neurosci, 2011, 65(1): 77-81 PMID: 21265939

[29]

SontagW, KalkaD. No effect of pulsed electromagnetic fields on PC12 and HL-60 cells. Radiat Environ Biophys, 2006, 45(1): 63-71 PMID: 16625396

[30]

VlachosA, Muller-DahlhausF, RosskoppJ, et al. . Repetitive magnetic stimulation induces functional and structural plasticity of excitatory postsynapses in mouse organotypic hippocampal slice cultures. J Neurosci, 2012, 32(48): 17514-17523 PMID: 23197741

[31]

GilioF, ConteA, VanacoreN, et al. . Excitatory and inhibitory after-effects after repetitive magnetic transcranial stimulation (rTMS) in normal subjects. Exp Brain Res, 2007, 176(4): 588-593 PMID: 16900360

[32]

YangTS, YangXH, ChenX, et al. . MicroRNA-106b in cancer-associated fibroblasts from gastric cancer promotes cell migration and invasion by targeting PTEN. FEBS Lett, 2014, 588(13): 2162-2169 PMID: 24842611

[33]

TanW, LiY, LimSG, et al. . miR-106b-25/miR-17-92 clusters: polycistrons with oncogenic roles in hepatocellular carcinoma. World J Gastroenterol, 2014, 20(20): 5962-5972 PMCID: 4033436 PMID: 24876719

[34]

SemoJ, SharirR, AfekA, et al. . The 106b~25 microRNA cluster is essential for neovascularization after hindlimb ischaemia in mice. Eur Heart J, 2013, 35(45): 3212-3223 PMID: 23420866

[35]

ZhangXY, TangLZ, RenBG, et al. . Interaction of MCM7 and RACK1 for activation of MCM7 and cell growth. Am J Pathol, 2013, 182(3): 796-805 PMCID: 3586685 PMID: 23313748

[36]

YingSY, ChangCP, LinSL. Intron-mediated RNA interference, intronic microRNAs, and applications. Methods Mol Biol, 2010, 629: 205-237 PMID: 20387152

[37]

LutterD, MarrC, KrumsiekJ, et al. . Intronic microRNAs support their host genes by mediating synergistic and antagonistic regulatory effects. BMC Genomics, 2010, 11: 224 PMCID: 2865499 PMID: 20370903

[38]

KippinTE, MartensDJ, van der KooyD. p21 loss compromises the relative quiescence of forebrain stem cell proliferation leading to exhaustion of their proliferation capacity. Genes Dev, 2005, 19(6): 756-767 PMCID: 1065728 PMID: 15769947

[39]

IveyKN, SrivastavaD. MicroRNAs as regulators of differentiation and cell fate decisions. Cell Stem Cell, 2010, 7(1): 36-41 PMID: 20621048

[40]

IvanovskaI, BallAS, DiazRL, et al. . MicroRNAs in the miR-106b family regulate p21/CDKN1A and promote cell cycle progression. Mol Cell Biol, 2008, 28(7): 2167-2174 PMCID: 2268421 PMID: 18212054

[41]

JoaquinM, GubernA, PosasF. A novel G1 checkpoint mediated by the p57 CDK inhibitor and p38 SAPK promotes cell survival upon stress. Cell Cycle, 2012, 11(18): 3339-3340 PMCID: 3466532 PMID: 22918239

[42]

KanT, SatoF, ItoT, et al. . The miR-106b-25 polycistron, activated by genomic amplification, functions as an oncogene by suppressing p21 and Bim. Gastroenterology, 2009, 136(5): 1689-1700 PMCID: 2887605 PMID: 19422085

[43]

NishiokaS, NakanoD, KitadaK, et al. . The cyclin- dependent kinase inhibitor p21 is essential for the beneficial effects of renal ischemic preconditioning on renal ischemia/reperfusion injury in mice. Kidney Int, 2013, 85(4): 871-879 PMID: 24336034

[44]

von HarsdorfR, HauckL, MehrhofF, et al. . E2F-1 overexpression in cardiomyocytes induces downregulation of p21CIP1 and p27KIP1 and release of active cyclin- dependent kinases in the presence of insulin-like growth factor I. Circ Res, 1999, 85(2): 128-136

[45]

PuriPL, BalsanoC, BurgioVL, et al. . MyoD prevents cyclinA/cdk2 containing E2F complexes formation in terminally differentiated myocytes. Oncogene, 1997, 14(10): 1171-1184 PMID: 9121766

[46]

Marques-TorrejonMA, PorlanE, BanitoA, et al. . Cyclin- dependent kinase inhibitor p21 controls adult neural stem cell expansion by regulating Sox2 gene expression. Cell Stem Cell, 2012, 12(1): 88-100 PMCID: 3714747 PMID: 23260487

[47]

MiyagiS, NishimotoM, SaitoT, et al. . The Sox2 regulatory region 2 functions as a neural stem cell-specific enhancer in the telencephalon. J Biol Chem, 2006, 281(19): 13374-13381 PMID: 16547000

[48]

LangeC, HuttnerWB, CalegariF. Cdk4/cyclinD1 overexpression in neural stem cells shortens G1, delays neurogenesis, and promotes the generation and expansion of basal progenitors. Cell Stem Cell, 2009, 5(3): 320-331 PMID: 19733543

[49]

LimS, KaldisP. Loss of Cdk2 and Cdk4 induces a switch from proliferation to differentiation in neural stem cells. Stem Cells, 2012, 30(7): 1509-1520 PMID: 22532528

[50]

DevganV, MammucariC, MillarSE, et al. . p21WAF1/Cip1 is a negative transcriptional regulator of Wnt4 expression downstream of Notch1 activation. Genes Dev, 2005, 19(12): 1485-1495 PMCID: 1151665 PMID: 15964998

AI Summary AI Mindmap
PDF

94

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/