Chondrogenic predifferentiation of human mesenchymal stem cells in collagen type I hydrogels

Standard

Chondrogenic predifferentiation of human mesenchymal stem cells in collagen type I hydrogels. / Fensky, Florian; Reichert, Johannes C; Traube, Andrea; Rackwitz, Lars; Siebenlist, Sebastian; Nöth, Ulrich.

in: BIOMED ENG-BIOMED TE, Jahrgang 59, Nr. 5, 01.10.2014, S. 375-383.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Fensky, F, Reichert, JC, Traube, A, Rackwitz, L, Siebenlist, S & Nöth, U 2014, 'Chondrogenic predifferentiation of human mesenchymal stem cells in collagen type I hydrogels', BIOMED ENG-BIOMED TE, Jg. 59, Nr. 5, S. 375-383. https://doi.org/10.1515/bmt-2013-0076

APA

Fensky, F., Reichert, J. C., Traube, A., Rackwitz, L., Siebenlist, S., & Nöth, U. (2014). Chondrogenic predifferentiation of human mesenchymal stem cells in collagen type I hydrogels. BIOMED ENG-BIOMED TE, 59(5), 375-383. https://doi.org/10.1515/bmt-2013-0076

Vancouver

Bibtex

@article{eb5ba6898794481594018e519d3f73a1,
title = "Chondrogenic predifferentiation of human mesenchymal stem cells in collagen type I hydrogels",
abstract = "Abstract Hyaline cartilage displays a limited regenerative potential. Consequently, therapeutic approaches have been developed to treat focal cartilage lesions. Larger-sized lesions are commonly treated by osteochondral grafting/mosaicplasty, autologous chondrocyte implantation (ACI) or matrix-induced chondrocyte implantation (MACI). As an alternative cell source to chondrocytes, multipotent mesenchymal stem cells (MSCs) are regarded a promising option. We therefore investigated the feasibility of predifferentiating human MSCs incorporated in hydrogels clinically applied for MACI (CaReS{\textregistered}). MSC-laden hydrogels were cast and cultured over 10 days in a defined chondrogenic differentiation medium supplemented with TGF-β1. This was followed by an 11-day culture in TGF-β1 free media. After 21 days, considerable contraction of the hydrogels was observed. Histochemistry showed cells of a chondrocyte-like morphology embedded in a proteoglycan-rich extracellular matrix. Real-time polymerase chain reaction (RT-PCR) analysis showed the expression of chondrogenic marker genes, such as collagen type II and aggrecan. In summary, we demonstrate that chondrogenic differentiation of human mesenchymal stem cells embedded in collagen type I hydrogels can be induced under the influence of TGF-β1 over a period of 10 days.",
author = "Florian Fensky and Reichert, {Johannes C} and Andrea Traube and Lars Rackwitz and Sebastian Siebenlist and Ulrich N{\"o}th",
year = "2014",
month = oct,
day = "1",
doi = "10.1515/bmt-2013-0076",
language = "English",
volume = "59",
pages = "375--383",
journal = "BIOMED ENG-BIOMED TE",
issn = "0013-5585",
publisher = "Walter de Gruyter GmbH & Co. KG",
number = "5",

}

RIS

TY - JOUR

T1 - Chondrogenic predifferentiation of human mesenchymal stem cells in collagen type I hydrogels

AU - Fensky, Florian

AU - Reichert, Johannes C

AU - Traube, Andrea

AU - Rackwitz, Lars

AU - Siebenlist, Sebastian

AU - Nöth, Ulrich

PY - 2014/10/1

Y1 - 2014/10/1

N2 - Abstract Hyaline cartilage displays a limited regenerative potential. Consequently, therapeutic approaches have been developed to treat focal cartilage lesions. Larger-sized lesions are commonly treated by osteochondral grafting/mosaicplasty, autologous chondrocyte implantation (ACI) or matrix-induced chondrocyte implantation (MACI). As an alternative cell source to chondrocytes, multipotent mesenchymal stem cells (MSCs) are regarded a promising option. We therefore investigated the feasibility of predifferentiating human MSCs incorporated in hydrogels clinically applied for MACI (CaReS®). MSC-laden hydrogels were cast and cultured over 10 days in a defined chondrogenic differentiation medium supplemented with TGF-β1. This was followed by an 11-day culture in TGF-β1 free media. After 21 days, considerable contraction of the hydrogels was observed. Histochemistry showed cells of a chondrocyte-like morphology embedded in a proteoglycan-rich extracellular matrix. Real-time polymerase chain reaction (RT-PCR) analysis showed the expression of chondrogenic marker genes, such as collagen type II and aggrecan. In summary, we demonstrate that chondrogenic differentiation of human mesenchymal stem cells embedded in collagen type I hydrogels can be induced under the influence of TGF-β1 over a period of 10 days.

AB - Abstract Hyaline cartilage displays a limited regenerative potential. Consequently, therapeutic approaches have been developed to treat focal cartilage lesions. Larger-sized lesions are commonly treated by osteochondral grafting/mosaicplasty, autologous chondrocyte implantation (ACI) or matrix-induced chondrocyte implantation (MACI). As an alternative cell source to chondrocytes, multipotent mesenchymal stem cells (MSCs) are regarded a promising option. We therefore investigated the feasibility of predifferentiating human MSCs incorporated in hydrogels clinically applied for MACI (CaReS®). MSC-laden hydrogels were cast and cultured over 10 days in a defined chondrogenic differentiation medium supplemented with TGF-β1. This was followed by an 11-day culture in TGF-β1 free media. After 21 days, considerable contraction of the hydrogels was observed. Histochemistry showed cells of a chondrocyte-like morphology embedded in a proteoglycan-rich extracellular matrix. Real-time polymerase chain reaction (RT-PCR) analysis showed the expression of chondrogenic marker genes, such as collagen type II and aggrecan. In summary, we demonstrate that chondrogenic differentiation of human mesenchymal stem cells embedded in collagen type I hydrogels can be induced under the influence of TGF-β1 over a period of 10 days.

U2 - 10.1515/bmt-2013-0076

DO - 10.1515/bmt-2013-0076

M3 - SCORING: Journal article

C2 - 24803605

VL - 59

SP - 375

EP - 383

JO - BIOMED ENG-BIOMED TE

JF - BIOMED ENG-BIOMED TE

SN - 0013-5585

IS - 5

ER -