Effect of a nerve graft substitute single-walled carbon nanotubes on rat pheochromocytoma cells

Qian Wu , Juan Zhang , Zheqin Hu

Journal of Wuhan University of Technology Materials Science Edition ›› 2015, Vol. 30 ›› Issue (4) : 847 -851.

PDF
Journal of Wuhan University of Technology Materials Science Edition ›› 2015, Vol. 30 ›› Issue (4) : 847 -851. DOI: 10.1007/s11595-015-1240-4
Biomaterials

Effect of a nerve graft substitute single-walled carbon nanotubes on rat pheochromocytoma cells

Author information +
History +
PDF

Abstract

Carbon nanotubes (CNTs) were extensively explored for their beneficial use in nervous system tissue engineering. However, an important concern regarding the use of CNTs is their toxicity during the interaction between cells and the nano particles. The rat pheochromocytoma cell line (PC12) was co-cultured with three types of single-walled carbon nanotubes (SWNTs), purified raw SWNTs (C), hydroxyl purified SWNTs (C-OH) and carboxyl purified SWNTs (C-COOH) at 25 µg/mL and 100 µg/ml. The experimental results revealed that SWNTs at the concentration below 100 µg/mL did not affect the cell viability. Notably, powerful antioxidant system in nerous system tissue is able to counteract with the toxicity of CNTs, which is characterized by the prominently enhanced expression of main antioxidant enzymes (catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx) and glutathione-S-transferase (GST)). Therefore, we believe that CNTs can be good candidates for the fabrication of biomedical scaffolds for the nerve tissue repair.

Keywords

nerve graft substitute / single-walled carbon nanotubes (SWNTs) / oxidative stress / PC12 cells

Cite this article

Download citation ▾
Qian Wu, Juan Zhang, Zheqin Hu. Effect of a nerve graft substitute single-walled carbon nanotubes on rat pheochromocytoma cells. Journal of Wuhan University of Technology Materials Science Edition, 2015, 30(4): 847-851 DOI:10.1007/s11595-015-1240-4

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Chao T I, Xiang S, Chen C S, et al. Carbon Nanotubes Promote Neuron Differentiation from Human Embryonic Stem Cells[J].. Biochem. Biophys. Res. Commun., 2009, 384: 426-430.

[2]

Lovat V, Pantarotto D, Lagostena L, et al. Carbon Nanotube Substrates Boost Neuronal Electrical Signaling[J].. Nano. Lett., 2005, 5: 1107-1110.

[3]

Cho Y, Borgens RB. The Effect of an Electrically Conductive Carbon Nanotube/Collagen Composite on Neurite Outgrowth of PC12 Cells[J].. J. Biomed. Mater. Res. A, 2010, 95: 510-517.

[4]

Cellot G, Cilia E, Cipollone S, et al. Carbon Nanotubes Might Improve Neuronal Performance by Favouring Electrical Shortcuts[J].. Nat. Nanotechnol., 2009, 4: 126-133.

[5]

Jan E, Kotov N A. Successful Differentiation of Mouse Neural Stem Cells on Layer-by-layer Assembled Single-walled Carbon Nanotube Composite[J].. Nano. Lett., 2007, 7: 1123-1128.

[6]

Zhao F, Zhao Y, Liu Y, et al. Cellular Uptake, Intracellular Trafficking, and Cytotoxicity of Nanomaterials[J].. Small, 2011, 7: 1322-1337.

[7]

Zhao Y, Xing G, Chai Z. Nanotoxicology: Are Carbon Nanotubes Safe?. Nat Nanotechnol, 2008, 3: 191-192.

[8]

Cui H F, Vashist S K, Al-Rubeaan K, et al. Interfacing Carbon Nanotubes with Living Mammalian Cells and Cytotoxicity Issues[J].. Chem. Res. Toxicol, 2010, 23: 1131-1147.

[9]

Jia G, Wang H, Yan L, et al. Cytotoxicity of Carbon Nanomaterials: Single-wall Nanotube, Multi-wall Nanotube, and Fullerence[J].. Environ Sci Technol, 2005, 39: 1378-1383.

[10]

Kaiser J P, Wick P, Manser P, et al. Single Walled Carbon Nanotubes (SWCNT) Affect Cell Physiology and Cell Architecture[J].. J. Mater. Sci. Mater. Med., 2008, 19: 1523-1527.

[11]

Oberdorster G, Sharp Z, Atudorei V, et al. Translocation of Inhaled Ultrafine Particles to the Brain[J].. Inhal. Toxicol, 2004, 16: 437-445.

[12]

Peters A, Veronesi B, Calderon-Garciduenas L, et al. Translocation and Potential Neurological Effects of Fine and Ultrafine Particles a Critical Update[J].. Part Fibre Toxicol, 2006, 3: 13.

[13]

Maes M, Galecki P, Chang YS, et al. A Review on the Oxidative and Nitrosative Stress Pathways in Major Depression and Their Possible Contribution to the (neuro) Degenerative Processes in that Illness[J].. Prog. NeuroPsychopharmacol. Biol. Psychiatry, 2011, 35: 676-692.

[14]

Kumar V, Gill K D. Oxidative Stress and Mitochondrial Dysfunction in Aluminium Neurotoxicity and Its Amelioration: A Review[J].. NeuroToxicology, 2014, 41: 676-692.

[15]

Wang J Y, Sun P P, Bao Y M, et al. Cytotoxicity of Single-walled Carbon Nanotubes on PC 12 Cells[J].. Toxico. In Vitro, 2011, 25: 242-250.

[16]

Wang J Y, Sun P P, Bao Y M, et al. Vitamin E Renders Protection to PC12 Cells Against Oxidative Damage and Apoptosis Induced by Single-walled Carbon Nanotubes[J].. Toxicol in Vitro, 2012, 26: 32-41.

[17]

Ansaria N, Khodagholia F, Aminib M, et al. Attenuation of LPSInduced Apoptosis in NGF-differentiated PC12 Cells Via NF-?B Pathway and Regulation of Cellular Redox Status by an Oxazine Derivative[J].. Biochimie., 2011, 93: 899-908.

[18]

Lu Y H, Su M Y, Huang H Y, et al. Protective Effects of the Citrus Flavanones to PC12 Cells Against Cytotoxicity Induced by Hydrogen Peroxide[J].. Neurosci. Lett., 2010, 484: 6-11.

[19]

Xiong Q, Xie P, Li H Y, et al. Acute Effects of Microcystins Exposure on the Transcription of Antioxidant Enzyme Genes in Three Organs (Liver, Kidney, and Testis) of Male Wistar Rats[J].. J. Biochem. Mol. Toxic., 2010, 24: 361-367.

[20]

Nel A, Xia T, Madler L, et al. Toxic Potential of Materials at Nanolevel[J].. Science, 2006, 311: 622-627.

[21]

Fulle S, Protasi F D, Tano G, et al. The Contribution of Reactive Oxygen Species to Sarcopenia and Muscle Ageing[J].. Exp. Gerontol., 2004, 39: 17-24.

[22]

Qiu T, Wu Q Z, Dai H L, et al. A Comparative Study on the Effects of Pristine and Functionalized Single-walled Carbon Nanotubes on Osteoblasts: Ultrastructural and Biochemical Properties[J].. J. Mater. Sci.: Mater. Med., 2014, 25: 1915-1923.

[23]

Pichardo S, Gutierrez-Praena D, Puerto M, et al. Oxidative Stress Responses to Carboxylic Acid Functionalized Single Wall Carbon Nanotubes on the Human Intestinal Cell Line Caco-2[J].. Toxicol in Vitro, 2012, 26: 672-677.

[24]

Qiu T, Yin Y X, Li B B, et al. PDLLA/PRGD/ß-TCP Conduits Build the Neurotrophin-rich Microenvironment Suppressing the Oxidative Stress and Promoting the Sciatic Nerve Regeneration[J].. J. Biomed. Mater. Res. A, 2014, 102: 3734-3743.

[25]

Raza H, John A. 4-Hydroxynonenal Induces Mitochondrial Oxidative Stress, Apoptosis and Expression of Glutathione S-transferase A4-4 and Cytochrome P450 in PC12 Cells[J].. Toxicol Appl. Pharm., 2006, 216: 309-318.

AI Summary AI Mindmap
PDF

104

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/