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Gene Silencing by RNA Interference in Neuron-like Cell Lines: in vitro SMA models.

Yıl 2020, Cilt: 42 Sayı: 2, 140 - 147, 17.03.2020
https://doi.org/10.20515/otd.497543

Öz

In order to explain
the biological mechanisms in the eukaryotic cells, cell lines are valuable
tools in cases where access to primary cells is limited. Although they do not
reflect primary cells exactly, cell lines are often needed and used to model
diseases in vitro. In this study, two neuron-like cell lines were used for gene
silencing by RNA interference to both evaluate advantages/disadvantages of
cells and their potential to be used as an in vitro models for
neurodegenerative diseaeses through spinal muscular atrophy. As in vitro SMA
models, SMN gene was knocked-down in both PC12 and NSC34 cell lines and gene
silencing was confirmed by Western blot and immunofluorescence stainings. We
found that SMN knock-down efficiencies were more than 90% in both PC12 and
NSC34 cell lines. We compared culture, differentiation and transfection
conditions of cell lines during silencing studies. Our findings will be helpful
for further studies using neuron-like PC12 and NSC34 cell lines. 

Kaynakça

  • 1. Lefebvre S, Bürglen L, Reboullet S,Clermont O,Burlet P,Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M, Le Paslier D, Frezal J, Cohen D, Weissenbach J, Munnich A, Melki J. Identification and Characterization of a Spinal Muscular Atrophy-Determining Gene. Cell, 1995; 80 (1): 155-165.
  • 2. Wirth B. An Update of the Mutation Spectrum of the Survival Motor Neuron Gene (SMN1) in Autosomal Recessive Spinal Muscular Atrophy (SMA).Hum Mutat. 2000;15(3):228-37.
  • 3. Erdem H, Pehlivan S, Topaloglu H, Ozguc M. Deletion Analysis in Turkish Patients with Spinal Muscular Atrophy. Brain Dev. 1999; 21: 86-89.
  • 4. Bowerman M, Shafey D, Kothary R. Smn Depletion Alters Profilin II Expression and Leads to Upregulation of the RhoA/ROCK Pathway and Defects in Neuronal Integrity. J. Mol. Neurosci. ; 2007; 32 (2): 120–131.
  • 5. Simic G, Mladinov M, Seso Simic D, Jovanov Milosevic N, Islam A, Pajtak A, Barisic N, Sertic J, Lucassen PJ, Hof PR, Kruslin B. Abnormal Motoneuron Migration, Differentiation, and Axon Outgrowth in Spinal Muscular Atrophy.Acta Neuropathol.2008;115(3):313-326.
  • 6. Rossoll W, Jablonka S, Andreassi C, Kröning AK, Karle K, Monani UR,Sendtner M. Smn, the Spinal Muscular Atrophy-determining Gene Product Modulates Axon Growth and Localization of Beta-actin mRNA in Growth Cones of Motoneurons. J Cell Biol. 2003; 163(4):801-12.
  • 7. McWhorter ML, Monani UR, Burghes AH, Beattie CE. Knockdown of the Survival Motor Neuron (Smn) Protein in Zebrafish Causes Defects in Motor Axon Outgrowth and Pathfinding.J Cell Biol. 2003;162(5):919-31.
  • 8. Bora-Tatar G, Erdem-Yurter H. Investigations of Curcumin and Resveratrol on Neurite Outgrowth: Perspectives on Spinal Muscular Atrophy. BioMed Res. Int. 2014;709108: 1-8.
  • 9. Freshney RI (2005). Culture of animal cells, A manual of basic techniques. 5th ed, WILEY-LISS.
  • 10. Greene LA, Tischler AS.Establishment of a Noradrenergic Clonal Line of Rat Adrenal Pheochromocytoma Cells which Respond to Nerve Growth Factor. Proc Natl Acad Sci U S A.1976; 73(7):2424-2428.
  • 11. Stevens, C.F. (1998).Culturing Nerve Cells. Culture and experimental use of the PC12 rat pheochromocytoma cell line. U.S.A.:Massachusetts Institute of Technology.
  • 12. Cashman NR, Durham HD, Blusztajn JK, Oda K, Tabira T,Shaw IT, Dahrouge S, Antel JP. Neuroblastoma x Spinal cord (NSC) Hybrid Cell Lines Resemble Developing Motor Neurons.Dev Dyn.1992; 194: 209–221.
  • 13. van Bergeijk J, Haastert K, Grothe C, Claus P.Valproic acid promotes neurite outgrowth in PC12 cells independent from regulation of the survival of motoneuron protein. Chem. Biol. Drug Des.2006; 67(3):244-247.
  • 14. Kim HD, Rossi JJ. RNAi Mechanisms and Applications. Biotechniques. 2008; 44(5):613-616.
  • 15. Farrell Jr RE. (2010).RNA methodologies. A laboratory guide for isolation and characterization. RNAi: take a RISC – role the Dicer,4th ed, Academic press.
  • 16. Hensel N, Ratzka A, Brinkmann H, Klimaschewski L, Grothe C, Claus P.Analysis of the Fibroblast Growth Factor System Reveals Alterations in a Mouse Model of Spinal Muscular Atrophy. PLoS One. 2012; 7: e31202.
  • 17. Maier O, Böhm J, Dahm M, Brück S, Beyer C, Johann S. Differentiated NSC-34 Motoneuron-like Cells as Experimental Model for Cholinergic Neurodegeneration. Neurochem Int. 2013; 62(8):1029-38.
  • 18. Zeng Z, Xu J, Zheng W. Artemisinin Protects PC12 Cells Against β-amyloid-Induced Apoptosis Through Activation of the ERK1/2 Signaling Pathway.Redox Biol. 2017; 12:625-633.
  • 19. Grau CM, Greene LA. Use of PC12 Cells and Rat Superior Cervical Ganglion Sympathetic Neurons as Models for Neuroprotective Assays Relevant to Prakinson’s Disease. Methods Mol Biol. 2012;846:201-11.
  • 20. Bahmad H, Hadadeh O, Chamaa F, Cheaito K, Darwish B, Makkawi AK, Abou-Kheir W.Modeling Human Neurological and Neurodegenerative Diseases: From Induced Pluripotent Stem Cells to Neuronal Differentiation and Its Applications in Neurotrauma. Front Mol Neurosci. 2017; 10: 50.
  • 21. Hensel N, Stockbrügger I, Rademacher S, Broughton N, Brinkmann H, Grothe C, Claus P. Bilateral Crosstalk of Rho- and Extracellular-signal-regulated-kinase (ERK) Pathways is Confined to an Unidirectional Mode in Spinal Muscular Atrophy (SMA).Cell Signal. 2014;26(3):540-548.

Nöron Benzeri Hücre Hatlarında RNA Interferans Aracılı Gen İfadesi Baskılama Çalışmaları: in vitro SMA modelleri

Yıl 2020, Cilt: 42 Sayı: 2, 140 - 147, 17.03.2020
https://doi.org/10.20515/otd.497543

Öz

Ökaryotik hücredeki
biyolojik olayların açıklanabilmesi amacıyla primer hücrelere ulaşımın kısıtlı
olduğu durumlarda hücre hatları kullanılmaktadır. Hücre hatları, primer
hücreleri birebir yansıtmamalarına karşın hastalık modeli oluşturmak için
sıklıkla ihtiyaç duyulan ve kullanılan hücrelerdir. Bu çalışmada genlerin
fonksiyonunun baskılanması prensibine dayanan RNA interferans yöntemi iki
farklı nöron benzeri hücre hatında uygulanmış, hücrelerin birbirlerine göre
avantajları/dezavantajları, nörodejeneratif bir hastalık olan Spinal müsküler
atrofi üzerinden karşılaştırılmıştır. In vitro SMA modeli oluşturmak üzere,
nöron benzeri hücrelere farklılaştırılan PC12 ve NSC34 hücre hatlarında SMN gen
ifadesi siRNA yöntemi ile baskılanmiş, baskılanma Western blot ve immünfloresan
boyama yöntemleri ile gösterilmiştir.PC12 ve NSC34 hücre hatlarında SMN gen
ifadesi %90’ın üzerinde baskılanabilmiş ve çalışmalar sırasında hücre
hatlarının kültür, farklılaşma, transfeksiyon koşulları arasındaki farklar
karşılaştırmalı olarak incelenmiştir. Elde ettiğimiz bulgular, ileride nöron
benzeri PC12 ve NSC34 hücre hatları kullanılarak gerçekleştirilecek çalışmalar
açısından yol gösterici olacaktır.

Kaynakça

  • 1. Lefebvre S, Bürglen L, Reboullet S,Clermont O,Burlet P,Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M, Le Paslier D, Frezal J, Cohen D, Weissenbach J, Munnich A, Melki J. Identification and Characterization of a Spinal Muscular Atrophy-Determining Gene. Cell, 1995; 80 (1): 155-165.
  • 2. Wirth B. An Update of the Mutation Spectrum of the Survival Motor Neuron Gene (SMN1) in Autosomal Recessive Spinal Muscular Atrophy (SMA).Hum Mutat. 2000;15(3):228-37.
  • 3. Erdem H, Pehlivan S, Topaloglu H, Ozguc M. Deletion Analysis in Turkish Patients with Spinal Muscular Atrophy. Brain Dev. 1999; 21: 86-89.
  • 4. Bowerman M, Shafey D, Kothary R. Smn Depletion Alters Profilin II Expression and Leads to Upregulation of the RhoA/ROCK Pathway and Defects in Neuronal Integrity. J. Mol. Neurosci. ; 2007; 32 (2): 120–131.
  • 5. Simic G, Mladinov M, Seso Simic D, Jovanov Milosevic N, Islam A, Pajtak A, Barisic N, Sertic J, Lucassen PJ, Hof PR, Kruslin B. Abnormal Motoneuron Migration, Differentiation, and Axon Outgrowth in Spinal Muscular Atrophy.Acta Neuropathol.2008;115(3):313-326.
  • 6. Rossoll W, Jablonka S, Andreassi C, Kröning AK, Karle K, Monani UR,Sendtner M. Smn, the Spinal Muscular Atrophy-determining Gene Product Modulates Axon Growth and Localization of Beta-actin mRNA in Growth Cones of Motoneurons. J Cell Biol. 2003; 163(4):801-12.
  • 7. McWhorter ML, Monani UR, Burghes AH, Beattie CE. Knockdown of the Survival Motor Neuron (Smn) Protein in Zebrafish Causes Defects in Motor Axon Outgrowth and Pathfinding.J Cell Biol. 2003;162(5):919-31.
  • 8. Bora-Tatar G, Erdem-Yurter H. Investigations of Curcumin and Resveratrol on Neurite Outgrowth: Perspectives on Spinal Muscular Atrophy. BioMed Res. Int. 2014;709108: 1-8.
  • 9. Freshney RI (2005). Culture of animal cells, A manual of basic techniques. 5th ed, WILEY-LISS.
  • 10. Greene LA, Tischler AS.Establishment of a Noradrenergic Clonal Line of Rat Adrenal Pheochromocytoma Cells which Respond to Nerve Growth Factor. Proc Natl Acad Sci U S A.1976; 73(7):2424-2428.
  • 11. Stevens, C.F. (1998).Culturing Nerve Cells. Culture and experimental use of the PC12 rat pheochromocytoma cell line. U.S.A.:Massachusetts Institute of Technology.
  • 12. Cashman NR, Durham HD, Blusztajn JK, Oda K, Tabira T,Shaw IT, Dahrouge S, Antel JP. Neuroblastoma x Spinal cord (NSC) Hybrid Cell Lines Resemble Developing Motor Neurons.Dev Dyn.1992; 194: 209–221.
  • 13. van Bergeijk J, Haastert K, Grothe C, Claus P.Valproic acid promotes neurite outgrowth in PC12 cells independent from regulation of the survival of motoneuron protein. Chem. Biol. Drug Des.2006; 67(3):244-247.
  • 14. Kim HD, Rossi JJ. RNAi Mechanisms and Applications. Biotechniques. 2008; 44(5):613-616.
  • 15. Farrell Jr RE. (2010).RNA methodologies. A laboratory guide for isolation and characterization. RNAi: take a RISC – role the Dicer,4th ed, Academic press.
  • 16. Hensel N, Ratzka A, Brinkmann H, Klimaschewski L, Grothe C, Claus P.Analysis of the Fibroblast Growth Factor System Reveals Alterations in a Mouse Model of Spinal Muscular Atrophy. PLoS One. 2012; 7: e31202.
  • 17. Maier O, Böhm J, Dahm M, Brück S, Beyer C, Johann S. Differentiated NSC-34 Motoneuron-like Cells as Experimental Model for Cholinergic Neurodegeneration. Neurochem Int. 2013; 62(8):1029-38.
  • 18. Zeng Z, Xu J, Zheng W. Artemisinin Protects PC12 Cells Against β-amyloid-Induced Apoptosis Through Activation of the ERK1/2 Signaling Pathway.Redox Biol. 2017; 12:625-633.
  • 19. Grau CM, Greene LA. Use of PC12 Cells and Rat Superior Cervical Ganglion Sympathetic Neurons as Models for Neuroprotective Assays Relevant to Prakinson’s Disease. Methods Mol Biol. 2012;846:201-11.
  • 20. Bahmad H, Hadadeh O, Chamaa F, Cheaito K, Darwish B, Makkawi AK, Abou-Kheir W.Modeling Human Neurological and Neurodegenerative Diseases: From Induced Pluripotent Stem Cells to Neuronal Differentiation and Its Applications in Neurotrauma. Front Mol Neurosci. 2017; 10: 50.
  • 21. Hensel N, Stockbrügger I, Rademacher S, Broughton N, Brinkmann H, Grothe C, Claus P. Bilateral Crosstalk of Rho- and Extracellular-signal-regulated-kinase (ERK) Pathways is Confined to an Unidirectional Mode in Spinal Muscular Atrophy (SMA).Cell Signal. 2014;26(3):540-548.
Toplam 21 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Sağlık Kurumları Yönetimi
Bölüm ORİJİNAL MAKALELER / ORIGINAL ARTICLES
Yazarlar

Gamze Bora 0000-0002-4206-8332

Yayımlanma Tarihi 17 Mart 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 42 Sayı: 2

Kaynak Göster

Vancouver Bora G. Nöron Benzeri Hücre Hatlarında RNA Interferans Aracılı Gen İfadesi Baskılama Çalışmaları: in vitro SMA modelleri. Osmangazi Tıp Dergisi. 2020;42(2):140-7.


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