Mesenchymal stem cells seeded onto nanofiber scaffold for myocardial regeneration

2021 ◽  
pp. 1-12
Author(s):  
Mohamed S. Kishta ◽  
Hanaa H. Ahmed ◽  
Mohamed A. M. Ali ◽  
Hadeer A. Aglan ◽  
Mohamed Ragaa Mohamed
2008 ◽  
Vol 149 (1) ◽  
pp. 47-56 ◽  
Author(s):  
Sasa Janjanin ◽  
Wan-Ju Li ◽  
Meredith T. Morgan ◽  
Rabie M. Shanti ◽  
Rocky S. Tuan

Author(s):  
Mahboobe Ghaedi ◽  
Masoud Soleimani ◽  
Iman Shabani ◽  
Yuyou Duan ◽  
Abbas Lotfi

AbstractThe emerging fields of tissue engineering and biomaterials have begun to provide potential treatment options for liver failure. The goal of the present study is to investigate the ability of a poly L-lactic acid (PLLA) nanofiber scaffold to support and enhance hepatic differentiation of human bone marrow-derived mesenchymal stem cells (hMSCs). A scaffold composed of poly L-lactic acid and collagen was fabricated by the electrospinning technique. After characterizing isolated hMSCs, they were seeded onto PLLA nanofiber scaffolds and induced to differentiate into a hepatocyte lineage. The mRNA levels and protein expression of several important hepatic genes were determined using RT-PCR, immunocytochemistry and ELISA. Flow cytometry revealed that the isolated bone marrow-derived stem cells were positive for hMSC-specific markers CD73, CD44, CD105 and CD166 and negative for hematopoietic markers CD34 and CD45. The differentiation of these stem cells into adipocytes and osteoblasts demonstrated their multipotency. Scanning electron microscopy showed adherence of cells in the nanofiber scaffold during differentiation towards hepatocytes. Our results showed that expression levels of liver-specific markers such as albumin, α-fetoprotein, and cytokeratins 8 and 18 were higher in differentiated cells on the nanofibers than when cultured on plates. Importantly, liver functioning serum proteins, albumin and α-1 antitrypsin were secreted into the culture medium at higher levels by the differentiated cells on the nanofibers than on the plates, demonstrating that our nanofibrous scaffolds promoted and enhanced hepatic differentiation under our culture conditions. Our results show that the engineered PLLA nanofibrous scaffold is a conducive matrix for the differentiation of MSCs into functional hepatocyte-like cells. This represents the first step for the use of this nanofibrous scaffold for culture and differentiation of stem cells that may be employed for tissue engineering and cell-based therapy applications.


2009 ◽  
Vol 9 ◽  
pp. 118-129 ◽  
Author(s):  
Markus D. Schofer ◽  
Ulrich Boudriot ◽  
Irini Leifeld ◽  
Romina I. Sütterlin ◽  
Markus Rudisile ◽  
...  

The aim of this study was to enhance synthetic poly(L-lactic acid) (PLLA) nanofibers by blending with collagen I (COLI) in order to improve their ability to promote growth and osteogenic differentiation of stem cellsin vitro. Fiber matrices composed of PLLA and COLI in different ratios were characterized with respect to their morphology, as well as their ability to promote growth of human mesenchymal stem cells (hMSC) over a period of 22 days. Furthermore, the course of differentiation was analyzed by gene expression of alkaline phosphatase (ALP), osteocalcin (OC), and COLI. The PLLA-COLI blend nanofibers presented themselves with a relatively smooth surface. They were more hydrophilic as compared to PLLA nanofibers alone and formed a gel-like structure with a stable nanofiber backbone when incubated in aqueous solutions. We examined nanofibers composed of different PLLA and COLI ratios. A composition of 4:1 ratio of PLLA:COLI showed the best results. When hMSC were cultured on the PLLA-COLI nanofiber blend, growth as well as osteoblast differentiation (determined as gene expression of ALP, OC, and COLI) was enhanced when compared to PLLA nanofibers alone. Therefore, the blending of PLLA with COLI might be a suitable tool to enhance PLLA nanofibers with respect to bone tissue engineering.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Karl F. Schüttler ◽  
Michael W. Bauhofer ◽  
Vanessa Ketter ◽  
Katja Giese ◽  
Daphne A. Eschbach ◽  
...  

2013 ◽  
Vol 9 (6) ◽  
pp. 6905-6914 ◽  
Author(s):  
C.N. Manning ◽  
A.G. Schwartz ◽  
W. Liu ◽  
J. Xie ◽  
N. Havlioglu ◽  
...  

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