Dergiler / Turkish Journal of Biology / 2016 / Cilt: 40 - Sayı: 2

Cardiomyogenic differentiation potential of human lipoaspirate-derivedstem cells on hyaluronic acid/gelatin plasma gels

Sayfa
369–379
Yayın Tarihi
2022-10-17
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The cardiac gene expression on HA/G plasma gels in the presence of activin-a + BMP-4 or insulin + valproic acid was more pronounced than in the presence of 5-azacytidine only, and scaffold and chemical modifier combinations were crucial for cardiomyogenic differentiation.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Cardiomyogenic differentiation from mesenchymal stem cells has emerged as a novel approach for repair of damaged myocardium.
📊
Temel Bulgular & Veri:In the present study, differentiation potential of human adipose-derived stem cells (ASCs) to cardiomyocytes has been investigated by growing them on hyaluronic acid/gelatin (HA/G) plasma gels and coverslips and supplementing the growth medium with chemical modifiers (activin-a, BMP-4, insulin, valproic acid, and 5-azacytidine) in various combinations.
💡
Sonuç & Katkı:The cardiac gene expression on HA/G plasma gels in the presence of activin-a + BMP-4 or insulin + valproic acid was more pronounced than in the presence of 5-azacytidine only, and scaffold and chemical modifier combinations were crucial for cardiomyogenic differentiation.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Cardiomyogenic differentiation from mesenchymal stem cells has emerged as a novel approach for repair of damaged myocardium. Cell transplantation through direct cell injection is not an optimal method due to the lack of cell-extracellular matrix interactions. In the present study, differentiation potential of human adipose-derived stem cells (ASCs) to cardiomyocytes has been investigated by growing them on hyaluronic acid/gelatin (HA/G) plasma gels and coverslips and supplementing the growth medium with chemical modifiers (activin-a, BMP-4, insulin, valproic acid, and 5-azacytidine) in various combinations. The HA/G plasma gels were produced from human blood plasma-derived fibrinogen, gelatin, and human umbilical cord-derived hyaluronic acid. A network-based approach was employed to select marker genes for cardiomyogenic differentiation, and the expression levels of three markers (GATA4, TBX5, and cTnI) were followed by RT-qPCR to investigate the cardiomyogenic differentiation potential of ASCs. Results indicated that each combination of chemical modifiers led to different expression levels in the aforementioned cardiac markers, and this was material-dependent, too. The cardiac gene expression on HA/G plasma gels in the presence of activin-a + BMP-4 or insulin + valproic acid was more pronounced than in the presence of 5-azacytidine only, and scaffold and chemical modifier combinations were crucial for cardiomyogenic differentiation.

🔖

Bu Makaleye Atıf Yap

GÖV, E., ARĞA, K. Y., KENAR, H., HALBUTOĞULLARI, Z. S., KARAGÖZ, E. (2022). Cardiomyogenic differentiation potential of human lipoaspirate-derivedstem cells on hyaluronic acid/gelatin plasma gels. Turkish Journal of Biology, Cilt: 40 - Sayı: 2, 369–379. https://ajindex.com/articles/600418

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (12)

  1. Alvord G, Roayaei J, Stephens R, Baseler MW, Lane HC, Lempicki RA (2007). The DAVID Gene Functional Classification Tool: a novel biological module-centric algorithm to functionally analyze large gene lists. Genome Biol 8: R183. Asumda FZ, Chase PB (2012). Nuclear cardiac troponin and tropomyosin are expressed early in cardiac differentiation of rat mesenchymal stem cells. Differentiation 83: 106–115.
  2. Bai X, Alt E (2010). Myocardial regeneration potential of adipose tissue-derived stem cells. Biochem Bioph Res Co 401: 321–326.
  3. Bai X, Yan Y, Song YH, Seidensticker M, Rabinovich B, Metzele R, Bankson JA, Vykoukal D, Alt E (2010). Both cultured and freshly isolated adipose tissue-derived stem cells enhance cardiac function after acute myocardial infarction. Eur Heart J 31: 489–501.
  4. Christman KL, Fok HH, Sievers RE, Fang Q, Lee RJ (2004). Fibrin glue alone and skeletal myoblasts in a fibrin scaffold preserve cardiac function after myocardial infarction. Tissue Eng 10: 403–409.
  5. Dimarakis I, Levicar N, Nihoyannopoulos P, Gordon MY, Habib NA (2006). In vitro stem cell differentiation into cardiomyocytes: Part 2: Chemicals, extracellular matrix, physical stimuli and coculture assays. J Cardiothor Ren Res 1: 115–121.
  6. Gomes AV, Potter JD, Szczesna-Cordary D (2002). The role of troponin in muscle contraction. IUBMB Life 54: 323–333.
  7. Hartung S, Schwanke K, Haase A, David R, Franz WM, Martin U, Zweigerdt R (2012). Directing cardiomyogenic differentiation of human pluripotent stem cells by plasmid-based transient overexpression of cardiac transcription factors. Stem Cells Dev 22: 1112–1125.
  8. Karagoz K, Raghu S, Arga KY (2015). Triple negative breast cancer: a multi-omics network discovery strategy for candidate targets and driving pathways. Omics 19: 115–130.
  9. Karaoz E, Doğan BN, Aksoy A, Gacar G, Akyüz S, Ayhan S, Genç ZS, Yürüker S, Duruksu G, Demircan PÇ (2010). Isolation and in vitro characterisation of dental pulp stem cells from natal teeth. Histochem Cell Biol 133: 95–112.
  10. Kattman SJ, Huber TL, Keller GM (2006). Multipotent Flk-1+ cardiovascular progenitor cells give rise to the cardiomyocyte, endothelial, and vascular smooth muscle lineages. Develop Cell 11: 723–732.
  11. Korurer E, Kenar H, Doger E, Karaoz E (2014). Production of a composite hyaluronic acid/gelatin blood plasma gel for hydrogel-based adipose tissue engineering applications. J Biomed Mater Res A 102: 2220–2229.
  12. Laflamme MA, Chen KY, Naumova AV, Muskheli V, Fugate JA, Dupras SK, Reinecke H, Xu C, Hassani