3D Poly(Lactic Acid) Scaffolds Promote Different Behaviors on Endothelial Progenitors and Adipose-Derived Stromal Cells in Comparison With Standard 2D Cultures

被引:14
作者
Biagini, Giuliana [1 ]
Senegaglia, Alexandra Cristina [2 ]
Pereira, Tarciso [3 ]
Berti, Lucas Freitas [3 ]
Marcon, Bruna Hilzendeger [1 ]
Stimamiglio, Marco Augusto [1 ]
机构
[1] Frocruz Parana, Inst Carlos Chagas, Lab Biol Basica Celulas Tronco, Curitiba, Parana, Brazil
[2] Pontificia Univ Catolica Parana, Escola Med, Nucleo Tecnol Celular, Curitiba, Parana, Brazil
[3] Univ Tecnol Fed Parana, Post Grad Program Biomed Engn, Dept Mech Engn, Curitiba, Parana, Brazil
关键词
mesenchymal stem cells; tissue engineering; 3D scaffold; expanded CD133+cells; poly(lactic acid)-PLA; MESENCHYMAL STEM-CELLS; UMBILICAL-CORD BLOOD; PLA SCAFFOLDS; BONE-MARROW; PRINTED PLA; TISSUE; CD133(+); CARTILAGE;
D O I
10.3389/fbioe.2021.700862
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Tissue engineering is a branch of regenerative medicine, which comprises the combination of biomaterials, cells and other bioactive molecules to regenerate tissues. Biomaterial scaffolds act as substrate and as physical support for cells and they can also reproduce the extracellular matrix cues. Although tissue engineering applications in cellular therapy tend to focus on the use of specialized cells from particular tissues or stem cells, little attention has been paid to endothelial progenitors, an important cell type in tissue regeneration. We combined 3D printed poly(lactic acid) scaffolds comprising two different pore sizes with human adipose-derived stromal cells (hASCs) and expanded CD133(+) cells to evaluate how these two cell types respond to the different architectures. hASCs represent an ideal source of cells for tissue engineering applications due to their low immunogenicity, paracrine activity and ability to differentiate. Expanded CD133(+) cells were isolated from umbilical cord blood and represent a source of endothelial-like cells with angiogenic potential. Fluorescence microscopy and scanning electron microscopy showed that both cell types were able to adhere to the scaffolds and maintain their characteristic morphologies. The porous PLA scaffolds stimulated cell cycle progression of hASCs but led to an arrest in the G1 phase and reduced proliferation of expanded CD133(+) cells. Also, while hASCs maintained their undifferentiated profile after 7 days of culture on the scaffolds, expanded CD133(+) cells presented a reduction of the von Willebrand factor (vWF), which affected the cells' angiogenic potential. We did not observe changes in cell behavior for any of the parameters analyzed between the scaffolds with different pore sizes, but the 3D environment created by the scaffolds had different effects on the cell types tested. Unlike the extensively used mesenchymal stem cell types, the 3D PLA scaffolds led to opposite behaviors of the expanded CD133(+) cells in terms of cytotoxicity, proliferation and immunophenotype. The results obtained reinforce the importance of studying how different cell types respond to 3D culture systems when considering the scaffold approach for tissue engineering.</p>
引用
收藏
页数:15
相关论文
共 60 条
  • [1] Porous scaffolds for bone regeneration
    Abbasi, Naghmeh
    Hamlet, Stephen
    Love, Robert M.
    Nguyen, Nam-Trung
    [J]. JOURNAL OF SCIENCE-ADVANCED MATERIALS AND DEVICES, 2020, 5 (01): : 1 - 9
  • [2] Engineering Biomaterials for Enhanced Tissue Regeneration
    Abbott R.D.
    Kaplan D.L.
    [J]. Current Stem Cell Reports, 2016, 2 (2) : 140 - 146
  • [3] Impact of 3-D printed PLA- and chitosan-based scaffolds on human monocyte/macrophage responses: Unraveling the effect of 3-D structures on inflammation
    Almeida, Catarina R.
    Serra, Tiziano
    Oliveira, Marta I.
    Planell, Josep A.
    Barbosa, Mario A.
    Navarro, Melba
    [J]. ACTA BIOMATERIALIA, 2014, 10 (02) : 613 - 622
  • [4] The Protein Content of Extracellular Vesicles Derived from Expanded Human Umbilical Cord Blood-Derived CD133+ and Human Bone Marrow-Derived Mesenchymal Stem Cells Partially Explains Why both Sources are Advantageous for Regenerative Medicine
    Angulski, Addeli B. B.
    Capriglione, Luiz G.
    Batista, Michel
    Marcon, Bruna H.
    Senegaglia, Alexandra C.
    Stimamiglio, Marco A.
    Correa, Alejandro
    [J]. STEM CELL REVIEWS AND REPORTS, 2017, 13 (02) : 244 - 257
  • [5] [Anonymous], 2012, ISO 10993-12Biological Evaluation of Medical Devices. Part 12: Sample Preparation and Reference Materials
  • [6] [Anonymous], 2010, 129 OECD
  • [7] Deconstructing the third dimension - how 3D culture microenvironments alter cellular cues
    Baker, Brendon M.
    Chen, Christopher S.
    [J]. JOURNAL OF CELL SCIENCE, 2012, 125 (13) : 3015 - 3024
  • [8] The CD133+ Cell as Advanced Medicinal Product for Myocardial and Limb Ischemia
    Bongiovanni, Dario
    Bassetti, Beatrice
    Gambini, Elisa
    Gaipa, Giuseppe
    Frati, Giacomo
    Achilli, Felice
    Scacciatella, Paolo
    Carbucicchio, Corrado
    Pompilio, Giulio
    [J]. STEM CELLS AND DEVELOPMENT, 2014, 23 (20) : 2403 - 2421
  • [9] Novel markers for the prospective isolation of human MSC
    Buehring, Hans-Joerg
    Battula, Venkata Lokesh
    Treml, Sabrina
    Schewe, Bernhard
    Kanz, Lothar
    Vogel, Wichard
    [J]. HEMATOPOIETIC STEM CELLS VI, 2007, 1106 : 262 - 271
  • [10] Biocompatibility and biodegradation of poly(lactic acid) (PLA) and an immiscible PLA/poly(ε-caprolactone) (PCL) blend compatibilized by poly(ε-caprolactone-b-tetrahydrofuran) implanted in horses
    Carvalho, Julia R. G.
    Conde, Gabriel
    Antonioli, Marina L.
    Dias, Paula P.
    Vasconcelos, Rosemeri O.
    Taboga, Sebastiao R.
    Canola, Paulo A.
    Chinelatto, Marcelo A.
    Pereira, Gener T.
    Ferraz, Guilherme C.
    [J]. POLYMER JOURNAL, 2020, 52 (06) : 629 - 643