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Åstrand, Carolina
Publikasjoner (3 av 3) Visa alla publikasjoner
Leino, M., Åstrand, C., Hughes-Brittain, N., Robb, B., McKean, R. & Chotteau, V. (2018). Human embryonic stem cell dispersion in electrospun PCL fiber scaffolds by coating with laminin-521 and E-cadherin-Fc. Journal of Biomedical Materials Research. Part B - Applied biomaterials, 106(3), 1226-1236
Åpne denne publikasjonen i ny fane eller vindu >>Human embryonic stem cell dispersion in electrospun PCL fiber scaffolds by coating with laminin-521 and E-cadherin-Fc
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2018 (engelsk)Inngår i: Journal of Biomedical Materials Research. Part B - Applied biomaterials, ISSN 1552-4973, E-ISSN 1552-4981, Vol. 106, nr 3, s. 1226-1236Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Advances in human pluripotent cell cultivation and differentiation protocols have led to production of stem cell-derived progenitors as a promising cell source for replacement therapy. Three-dimensional (3-D) culture is a better mimic of the natural niche for stem cells and is widely used for disease modeling. Here, we describe a nonaggregate culture system of human embryonic stem cells inside electrospun polycaprolactone (PCL) fiber scaffolds combined with defined extracellular proteins naturally occurring in the stem cell niche. PCL fiber scaffolds coated with recombinant human laminin-521 readily supported initial stem cell attachment and growth from a single-cell suspension. The combination of recombinant E-cadherin-Fc and laminin-521 further improved cell dispersion rendering a uniform cell population. Finally, we showed that the cells cultured in E-cadherin-Fc- and laminin-521-coated PCL scaffolds could differentiate into all three germ layers. Importantly, we provided a chemically defined 3-D system in which pluripotent stem cells grown and differentiated avoiding the formation of cell aggregates.

sted, utgiver, år, opplag, sider
Wiley, 2018
Emneord
pluripotent stem cells, electrospun scaffold, PCL, three-dimensional culture, extracellular matrix coating
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-225172 (URN)10.1002/jbm.b.33928 (DOI)000427068200030 ()28577328 (PubMedID)2-s2.0-85020120426 (Scopus ID)
Forskningsfinansiär
EU, FP7, Seventh Framework Programme, 2-2013-601700
Merknad

QC 20180404

Tilgjengelig fra: 2018-04-04 Laget: 2018-04-04 Sist oppdatert: 2018-04-11bibliografisk kontrollert
Ravichandran, R., Åstrand, C., Patra, H. K., Turner, A. P. F., Chotteau, V. & Phopase, J. (2017). Intelligent ECM mimetic injectable scaffolds based on functional collagen building blocks for tissue engineering and biomedical applications. RSC Advances, 7(34), 21068-21078
Åpne denne publikasjonen i ny fane eller vindu >>Intelligent ECM mimetic injectable scaffolds based on functional collagen building blocks for tissue engineering and biomedical applications
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2017 (engelsk)Inngår i: RSC Advances, ISSN 2046-2069, E-ISSN 2046-2069, Vol. 7, nr 34, s. 21068-21078Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Hydrogels comprising natural extracellular matrix (ECM) components are very attractive as scaffolds for regenerative medicine applications due to their inherent biointeractive properties. Responsive materials that adapt to their surrounding environments and regulate transport of ions and bioactive molecules manifest significant advantages for biomedical applications. Although there are many exciting challenges, the opportunity to design, fabricate and engineer stimuli-responsive polymeric systems based on ECM components is particularly attractive for regenerative medicine. Here we describe a one-pot approach to fabricate in situ fast gellable intelligent ECM mimetic scaffolds, based on methacrylated collagen building blocks with mechanical properties that can be modulated in the kPa-MPa range and that are suitable for both soft and hard tissues. Physiochemical characterizations demonstrate their temperature and pH responsiveness, together with the structural and enzymatic resistance that make them suitable scaffolds for long-term use in regenerative medicine and biomedical applications. The multifunctionality of these hydrogels has been demonstrated as an in situ depot-forming delivery platform for the adjustable controlled release of proteins and small drug molecules under physiological conditions and as a structural support for adhesion, proliferation and metabolic activities of human cells. The results presented herein should be useful to the design and fabrication of tailor-made scaffolds with tunable properties that retain and exhibit sustained release of growth factors for promoting tissue regeneration.

sted, utgiver, år, opplag, sider
ROYAL SOC CHEMISTRY, 2017
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-207725 (URN)10.1039/c7ra02927f (DOI)000399722300040 ()2-s2.0-85018519019 (Scopus ID)
Merknad

QC 20170524

Tilgjengelig fra: 2017-05-24 Laget: 2017-05-24 Sist oppdatert: 2017-11-29bibliografisk kontrollert
Al-Khalili, L., Gillner, K., Zhang, Y., Åstrand, C., Shokri, A., Hughes-Brittain, N., . . . Chotteau, V. (2016). Characterization of Human CD133+Cells in Biocompatible Poly(l-lactic acid) Electrospun Nano-Fiber Scaffolds. Journal of Biomaterials and Tissue Engineering, 6(12), 959-966
Åpne denne publikasjonen i ny fane eller vindu >>Characterization of Human CD133+Cells in Biocompatible Poly(l-lactic acid) Electrospun Nano-Fiber Scaffolds
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2016 (engelsk)Inngår i: Journal of Biomaterials and Tissue Engineering, ISSN 2157-9083, E-ISSN 2157-9091, Vol. 6, nr 12, s. 959-966Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

CD133+ cells are potential myogenic progenitors for skeletal muscle regeneration to treat muscular dystrophies. The proliferation of human CD133+ stem cells was studied for 14 days in 3D biomimetic electrospun poly-L-lactic acid (PLLA) nano-fiber scaffolds. Additionally, the myogenic differentiation of the cells was studied during the last 7 days of the culture period. The cells were homogeneously distributed in the 3D scaffolds while colony formation and myotube formation occurred in 2D. After a lag phase due to lower initial cell attachment and an adaptation period, the cell growth rate in 3D was comparable to 2D after 7 and 14 days of culture. The expression of the stem cell (SC) marker PAX7 was 1.5-fold higher in 3D than 2D while the differentiation markers MyoG, Desmin and MyoD were only slightly changed (or remain unchanged) in 3D but strongly increased in 2D (12.6, 3.9, and 7.9-fold), and the myotube formation observed in 2D was absent in 3D. The marker expression during proliferation and differentiation, together with the absence of myotubes in 3D, indicates a better maintenance of stemness in 3D PLLA and stronger tendency for spontaneous differentiation in 2D culture. This makes 3D PLLA a promising biomaterial for the expansion of functional CD133+ cells.

sted, utgiver, år, opplag, sider
American Scientific Publishers, 2016
Emneord
Myogenic Progenitor Cell, CD133+Cells, Myogenic Differentiation, 3D Cell Culturing, Electrospun Biodegradable Nano-Fiber Scaffold
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-198952 (URN)10.1166/jbt.2016.1531 (DOI)000387148500005 ()2-s2.0-84998636398 (Scopus ID)
Forskningsfinansiär
EU, FP7, Seventh Framework Programme
Merknad

QC 20170113

Tilgjengelig fra: 2017-01-13 Laget: 2016-12-22 Sist oppdatert: 2017-11-29bibliografisk kontrollert
Organisasjoner