Öz
Aim: As being a
heterogenous population but having different pools of self-renewing cells,
amniotic fluid cells (AFCs) have been considered as promising cell sources for
regenerative medicine owing to their multipotency and effective reprogramming
capacity. AFCs can more easily and effectively be
reprogrammed than terminally differentiated cells to generate induced
pluripotent stem cells (iPSCs) by transfectional and chemical strategies. But
stem cell dynamics and differentiation capacity of AFCs into multiple lineages
were poorly understood. The aim of this study was to determine the expression
and stem cell characteristics of stem cell pluripotency markers in amniotic
fluid cells. Methods: In this study,
the expression profile of pluripotency markers in AFCs taken from 17 patients
were investigated by conventional RT-PCR by qualitatively. Results: The results showed that all the
pluripotency markers (OCT3/OCT4, SOX2, KLF4, MYC,
KIT, NANOG, DPPA3, DPPA5, FUT4, SALL4) were expressed in AFCs from different
patients but UTF1 is shows a
non-specific expression. Conclusion:
Consequently, our results revealed that AFCs have a unique stem cell profile
and pluripotency markers may be impactful when choosing cells for reprogramming
and regenerative medicine applications.
Anahtar Kelimeler
Amniotic fluid cells pluripotency markers expression regenerative medicine
Kaynakça
- 1. Roubelakis MG, Trohatou O, Anagnou NP. Amniotic fluid and amniotic membrane stem cells: marker discovery. Stem Cells International 2012, 107836.
- 2. Gholizadeh-Ghalehaziz S, Farahzadi R, Fathi E, Pashaiasl M. A mini overview of isolation, characterization and application of amniotic fluid stem cells. International Journal of Stem Cells 2015; 8(2): 115-120.
- 3. Klemmt PA, Vafaizadeh V, Groner B. The potential of amniotic fluid stem cells for cellular therapy and tissue engineering. Expert Opin Biol Ther 2011; 11(10): 1297-1314.
- 4. Galende E, Karakikes I, Edelman L, Desnick AJ, Kerenyi T, Khoueiry G, Lafferty J, McGinn JT, Brodman M, Fuster V, Hajjar R, Polgar K. Amniotic fluid cells are more efficiently reprogrammed to pluripotency than adult cells. Cellular Reprograming 2010; 12(2): 117-125.
- 5. Roubelakis MG, Pappa KI, Bitsika V, Zagoura D, Vlahou A, Papadaki HA, Antsaklis A, Anagnou NP. Molecular and proteomic characterization of human mesenchymal stem cells derived from amniotic fluid: comparison to bone marrow mesenchymal stem cells. Stem Cells Dev 2007; 16(6): 931-952.
- 6. Li C, Zhou J, Shi G, Ma Y, Yang Y, Gu J, Yu H, Jin S, Wei Z, Chen F, Jin Y. Pluripotency can be rapidly and efficiently induced in human amniotic fluid-derived cells. Human Molecular Genetics 2009; 18(22): 4340-4349.
- 7. Ditadi A, Coppi P, Picone O, Gautreau L, Smati R, Six E, Bonhomme D, Ezine S, Frydman R, Cavazzana-Calvo M, Andre-Schmutz I. Human and murine amniotic fluid c-Kit+/Lin- cells display hematopoietic activity. Blood 2017; 113(17): 3953-3960.
- 8. Bossolasco P, Montemurro T, Cova L, Zangrossi S, Calzarossa C, Buiatiotis S, Soligo D, Bosari S, Silani V, Deliliers LG, Rebulla P, Lazzari L. Molecular and phenotypic characterization of human amniotic fluid cells and their differentiation potential. Cell Research 2006; 16: 329-336.
- 9. Kang JH, Park HJ, Jung YW, Shim SH, Sung SR, Park JE, Cha DH, Ahn EH. Comparative transriptome analysis of cell-free fetal RNA from amniotic fluid an RNA from amniocytes in uncomplicated pregnancies. Plos One 2015;10(7):1-13.
- 10. Chen L., Daley GQ. Molecular basis of pluripotency. Human Molecular Genetics 2008; 17(1): 23-27.
- 11. Liu X, Huang J, Chen T, Wang Y, Xin S, Li J, Pei G, Kang J. Yamanaka factors critically regulate the developmental signaling network in mouse embryonic stem cells. Cell Research 2008; 18: 1177-1189.
- 12. Zhao W, Ji X, Zhang F, Li L, Ma L. Embryonic stem cell markers. Molecules 2012; 17: 6196-6236.
- 13. Pazhanisamy S. Adult stem cells and embryonic stem cell markers. Mater Methods 2013; 3: 200.
- 14. Feng C, Jia YD, Zhao XY. Pluripotency of induced pluripotent stem cells. Genomics Proteomics Bioinformatics 2013; 11: 299-303.
- 15. Ramirez JM, Gerbal-Chaloin S, Milhavet O, Qiang B, Becker F, Assou S, Lemaitre JM, Hamamah S, De Vos J. Brief report: benchmarking human pluripotent stem cell markers during differentiation into the three germ layers unveils a striking heterogenity – all markers are not equal. Stem Cells 2011; 29:1469-1474.
- 16. Maguire CT, Demarest BL, Hill JT, Palmer JD, Brothman AR, Yost HJ, Condic ML. Genome-wide analysis reveals the unique stem cell identity of human amniocytes. PloS One 2013; 8(1): 1-16.
- 17. Chomczynski P, Sacchi N. Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction. Anal Biochem 1987; 162(1): 156-159.
- 18. Kunsaki SM, Freedman DA, Fauza DO. Fetal tracheal reconstruction with cartiaginous grafts engineered from mesenchymal amniocytes. Journal of Pediatric Surgery 2006; 41: 675-682.
- 19. Gekas J, Walther G, Skuk D, Bujold E, Harvey I, Franc O, Bertrand F. In-vitro and in-vivo study of human amniotic fluid-derived stem cell differentiation into myogenic lineage. Clinical Experimental Medicine 2010; 10: 1-6.
- 20. Ge X, Wang IE, Toma I, Sebastiano V, Liu J, Butte MJ, Pera RAR, Yang PC. Human mesenchymal stem cell-derived induced pluripotent sttem cells may generate a universal source of cardiac cells. Stem Cells and Development 2012; 21(15): 2798-2808.
- 21. Anchan RM, Quaas P, Gerami-Naini B, Bartake H, Griffin A, Zhou Y, Eaton JL, George LL, Naber C, Turbe-Doan A, Park JP, Hornstein MD, Maas RL. Amniocytes can serve a dual function as a source of iPS cells and feeder layers. Human Molecular Genetics 2011; 20(5): 962-974.
- 22. Kunisaki SM, Armant M, Kao SG, Stevenson K, Kim H, Fauza DO. Tissue engineering from human mesenchymal amniocytes: a prelude to clinical trials. Journal of Pediatric Surgery 2007; 42: 974-980.
- 23. Kaviani A, Guleserian K, Perry TE, Jenningd RW, Ziegler MM, Fauza DO. Fetal tissue engineering from amniotic fluid. Journal of the American College of Surgeons 2003; 196: 592-597.
Öz
Amaç: Amniyotik sıvı farklı
seviyelerde kendini yenileyebilen hücre gruplarından oluşmaktadır ve bu
hücrelerin kök hücre özellikleri henüz tam olarak karakterize edilmemiştir. Son
yıllarda amniyotik sıvı hücreleri (AFC) rejenaratif tıp için umut veren kök hücre
kaynağı olarak görülmektedir. AFC’ler transfeksiyonel ve kimyasal stratejiler
ile indüklenmiş pluripotent kök hücre (iPSC)’ler oluşturmak için terminal
olarak farklılaşmış hücrelerden daha kolay ve etkili bir şekilde yeniden
programlanabilirler. Fakat AFC’lerin kök hücre potansiyelleri ve farklı hücre
soylarına farklılaşma kapasitesi tam olarak anlaşılamamıştır. Bu çalışmada amniyotik
sıvı hücrelerinde kök hücre pluripotensi belirteçlerinin ifadelerinin ve kök
hücre karakterlerinin belirlenmesi amaçlanmıştır.
Yöntem: Bu çalışmada, 17 amniyon
sıvısından elde edilen AFC’lerde pluripotensi belirteçlerinin ifade edilip
edilmediği geleneksel RT-PCR ile kalitatif olarak araştırılmıştır. Bulgular: Elde edilen sonuçlar, farklı
hastalardan alınan AFC örneklerinde incelenen pluripotensi belirteçlerinden OCT3/OCT4, SOX2, KLF4, MYC, KIT, NANOG,
DPPA3, DPPA5, FUT4, SALL4’ün ifade edildiğini, UTF1 için ise non-spesifik
ifade olduğunu göstermektedir.
Sonuç: Elde edilen bulgular doğrultusunda
AFC’nin kendine özgü bir kök hücre profiline sahip olduğu ve pluripotensi
belirteçlerinin yeniden programlama ve rejeneratif tıp uygulamaları için hücre
seçiminde etkili şekilde kullanılabileceği düşünülmektedir.
Anahtar Kelimeler
Amniyotik sıvı hücresi pluripotensi belirteci ekspresyon rejeneratif tıp
Kaynakça
- 1. Roubelakis MG, Trohatou O, Anagnou NP. Amniotic fluid and amniotic membrane stem cells: marker discovery. Stem Cells International 2012, 107836.
- 2. Gholizadeh-Ghalehaziz S, Farahzadi R, Fathi E, Pashaiasl M. A mini overview of isolation, characterization and application of amniotic fluid stem cells. International Journal of Stem Cells 2015; 8(2): 115-120.
- 3. Klemmt PA, Vafaizadeh V, Groner B. The potential of amniotic fluid stem cells for cellular therapy and tissue engineering. Expert Opin Biol Ther 2011; 11(10): 1297-1314.
- 4. Galende E, Karakikes I, Edelman L, Desnick AJ, Kerenyi T, Khoueiry G, Lafferty J, McGinn JT, Brodman M, Fuster V, Hajjar R, Polgar K. Amniotic fluid cells are more efficiently reprogrammed to pluripotency than adult cells. Cellular Reprograming 2010; 12(2): 117-125.
- 5. Roubelakis MG, Pappa KI, Bitsika V, Zagoura D, Vlahou A, Papadaki HA, Antsaklis A, Anagnou NP. Molecular and proteomic characterization of human mesenchymal stem cells derived from amniotic fluid: comparison to bone marrow mesenchymal stem cells. Stem Cells Dev 2007; 16(6): 931-952.
- 6. Li C, Zhou J, Shi G, Ma Y, Yang Y, Gu J, Yu H, Jin S, Wei Z, Chen F, Jin Y. Pluripotency can be rapidly and efficiently induced in human amniotic fluid-derived cells. Human Molecular Genetics 2009; 18(22): 4340-4349.
- 7. Ditadi A, Coppi P, Picone O, Gautreau L, Smati R, Six E, Bonhomme D, Ezine S, Frydman R, Cavazzana-Calvo M, Andre-Schmutz I. Human and murine amniotic fluid c-Kit+/Lin- cells display hematopoietic activity. Blood 2017; 113(17): 3953-3960.
- 8. Bossolasco P, Montemurro T, Cova L, Zangrossi S, Calzarossa C, Buiatiotis S, Soligo D, Bosari S, Silani V, Deliliers LG, Rebulla P, Lazzari L. Molecular and phenotypic characterization of human amniotic fluid cells and their differentiation potential. Cell Research 2006; 16: 329-336.
- 9. Kang JH, Park HJ, Jung YW, Shim SH, Sung SR, Park JE, Cha DH, Ahn EH. Comparative transriptome analysis of cell-free fetal RNA from amniotic fluid an RNA from amniocytes in uncomplicated pregnancies. Plos One 2015;10(7):1-13.
- 10. Chen L., Daley GQ. Molecular basis of pluripotency. Human Molecular Genetics 2008; 17(1): 23-27.
- 11. Liu X, Huang J, Chen T, Wang Y, Xin S, Li J, Pei G, Kang J. Yamanaka factors critically regulate the developmental signaling network in mouse embryonic stem cells. Cell Research 2008; 18: 1177-1189.
- 12. Zhao W, Ji X, Zhang F, Li L, Ma L. Embryonic stem cell markers. Molecules 2012; 17: 6196-6236.
- 13. Pazhanisamy S. Adult stem cells and embryonic stem cell markers. Mater Methods 2013; 3: 200.
- 14. Feng C, Jia YD, Zhao XY. Pluripotency of induced pluripotent stem cells. Genomics Proteomics Bioinformatics 2013; 11: 299-303.
- 15. Ramirez JM, Gerbal-Chaloin S, Milhavet O, Qiang B, Becker F, Assou S, Lemaitre JM, Hamamah S, De Vos J. Brief report: benchmarking human pluripotent stem cell markers during differentiation into the three germ layers unveils a striking heterogenity – all markers are not equal. Stem Cells 2011; 29:1469-1474.
- 16. Maguire CT, Demarest BL, Hill JT, Palmer JD, Brothman AR, Yost HJ, Condic ML. Genome-wide analysis reveals the unique stem cell identity of human amniocytes. PloS One 2013; 8(1): 1-16.
- 17. Chomczynski P, Sacchi N. Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction. Anal Biochem 1987; 162(1): 156-159.
- 18. Kunsaki SM, Freedman DA, Fauza DO. Fetal tracheal reconstruction with cartiaginous grafts engineered from mesenchymal amniocytes. Journal of Pediatric Surgery 2006; 41: 675-682.
- 19. Gekas J, Walther G, Skuk D, Bujold E, Harvey I, Franc O, Bertrand F. In-vitro and in-vivo study of human amniotic fluid-derived stem cell differentiation into myogenic lineage. Clinical Experimental Medicine 2010; 10: 1-6.
- 20. Ge X, Wang IE, Toma I, Sebastiano V, Liu J, Butte MJ, Pera RAR, Yang PC. Human mesenchymal stem cell-derived induced pluripotent sttem cells may generate a universal source of cardiac cells. Stem Cells and Development 2012; 21(15): 2798-2808.
- 21. Anchan RM, Quaas P, Gerami-Naini B, Bartake H, Griffin A, Zhou Y, Eaton JL, George LL, Naber C, Turbe-Doan A, Park JP, Hornstein MD, Maas RL. Amniocytes can serve a dual function as a source of iPS cells and feeder layers. Human Molecular Genetics 2011; 20(5): 962-974.
- 22. Kunisaki SM, Armant M, Kao SG, Stevenson K, Kim H, Fauza DO. Tissue engineering from human mesenchymal amniocytes: a prelude to clinical trials. Journal of Pediatric Surgery 2007; 42: 974-980.
- 23. Kaviani A, Guleserian K, Perry TE, Jenningd RW, Ziegler MM, Fauza DO. Fetal tissue engineering from amniotic fluid. Journal of the American College of Surgeons 2003; 196: 592-597.
Ayrıntılar
| Birincil Dil | Türkçe |
|---|---|
| Konular | Sağlık Kurumları Yönetimi |
| Bölüm | Araştırma Makalesi |
| Yazarlar | |
| Yayımlanma Tarihi | 31 Aralık 2019 |
| Gönderilme Tarihi | 27 Eylül 2019 |
| Kabul Tarihi | 22 Ekim 2019 |
| Yayımlandığı Sayı | Yıl 2019 Cilt: 12 Sayı: 3 |
Kaynak Göster
MEÜ
Sağlık Bilimleri Dergisi Doç.Dr. Gönül Aslan'ın Editörlüğünde Mersin
Üniversitesi Sağlık Bilimleri Enstitüsüne bağlı olarak 2008 yılında
yayımlanmaya başlanmıştır. Prof.Dr. Gönül Aslan Mart 2015 tarihinde Başeditörlük görevine Prof.Dr.
Caferi Tayyar Şaşmaz'a devretmiştir. 01 Ocak 2023 tarihinde Prof.Dr. C. Tayyar Şaşmaz Başeditörlük görevini Prof.Dr. Özlem İzci Ay'a devretmiştir.
Yılda üç sayı olarak (Nisan - Ağustos - Aralık) yayımlanan dergi multisektöryal hakemli bir bilimsel dergidir. Dergide araştırma makaleleri yanında derleme, olgu sunumu ve editöre mektup tipinde bilimsel yazılar yayımlanmaktadır. Yayın hayatına başladığı günden beri eposta yoluyla yayın alan ve hem online hem de basılı olarak yayımlanan dergimiz, Mayıs 2014 sayısından itibaren sadece online olarak yayımlanmaya başlamıştır. TÜBİTAK-ULAKBİM Dergi Park ile Nisan 2015 tarihinde yapılan Katılım Sözleşmesi sonrasında online yayın kabul ve değerlendirme sürecine geçmiştir.
Mersin Üniversitesi Sağlık Bilimleri Dergisi 16 Kasım 2011'dan beri Türkiye Atıf Dizini tarafından indekslenmektedir.
Mersin Üniversitesi Sağlık Bilimleri Dergisi 2016 birinci sayıdan itibaren ULAKBİM Tıp Veri Tabanı tarafından indekslenmektedir.
Mersin Üniversitesi Sağlık Bilimleri Dergisi 02 Ekim 2019'dan beri DOAJ tarafından indekslenmektedir.
Mersin Üniversitesi Sağlık Bilimleri Dergisi 23 Mart 2021'den beri EBSCO tarafından indekslenmektedir.
Dergimiz açık erişim politikasını benimsemiş olup, dergimizde makale başvuru, değerlendirme ve yayınlanma aşamasında ücret talep edilmemektedir. Dergimizde yayımlanan makalelerin tamamına ücretsiz olarak Arşivden erişilebilmektedir.
Bu eser Creative Commons Atıf-GayriTicari 4.0 Uluslararası Lisansı ile lisanslanmıştır.