## Abstract Availability of human embryonic stem cells (hESC) has enhanced human neural differentiation research. The derivation of neural progenitor (NP) cells from hESC facilitates the interrogation of human embryonic development through the generation of neuronal subtypes and supporting glial ce
Direct and progressive differentiation of human embryonic stem cells into the chondrogenic lineage
โ Scribed by Guochun Gong; Deborah Ferrari; Caroline N. Dealy; Robert A. Kosher
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 422 KB
- Volume
- 224
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
Treatment of common and debilitating degenerative cartilage diseases particularly osteoarthritis is a clinical challenge because of the limited capacity of the tissue for selfโrepair. Because of their unlimited capacity for selfโrenewal and ability to differentiate into multiple lineages, human embryonic stem cells (hESCs) are a potentially powerful tool for repair of cartilage defects. The primary objective of the present study was to develop culture systems and conditions that enable hESCs to directly and uniformly differentiate into the chondrogenic lineage without prior embryoid body (EB) formation, since the inherent cellular heterogeneity of EBs hinders obtaining homogeneous populations of chondrogenic cells that can be used for cartilage repair. To this end, we have subjected undifferentiated pluripotent hESCs to the high density micromass culture conditions we have extensively used to direct the differentiation of embryonic limb bud mesenchymal cells into chondrocytes. We report that micromass cultures of pluripotent hESCs undergo direct, rapid, progressive, and substantially uniform chondrogenic differentiation in the presence of BMP2 or a combination of BMP2 and TGFโฮฒ1, signaling molecules that act in concert to regulate chondrogenesis in the developing limb. The gene expression profiles of hESCโderived cultures harvested at various times during the progression of their differentiation has enabled us to identify cultures comprising cells in different phases of the chondrogenic lineage ranging from cultures just entering the lineage to well differentiated chondrocytes. Thus, we are poised to compare the abilities of hESCโderived progenitors in different phases of the chondrogenic lineage for cartilage repair. J. Cell. Physiol. 224: 664โ671, 2010. ยฉ 2010 WileyโLiss, Inc.
๐ SIMILAR VOLUMES
## Abstract Pluripotent embryonic stem (ES) cells have the capability to differentiate to various cell types and may represent an alternative cell source for the treatment of cartilage defects. Here, we show that differentiation of ES cells toward the chondrogenic lineage can be enhanced by alterin
## Abstract Availability of human chondrocytes is a major limiting factor regarding drug discovery projects and tissue replacement therapies. As an alternative human mesenchymal stem cells (hMSCs) from bone marrow are taken into consideration as they can differentiate along the chondrogenic lineage
## Abstract The chondrogenic differentiation of bone marrowโderived human mesenchymal stem cells (MSCs) in a collagen type I hydrogel, which is in clinical use for matrixโbased autologous chondrocyte transplantation (ACT), was investigated. Collagen hydrogels with 2.5 ร 10^5^ MSCs/mL were fabricate
Electromagnetic fields (EMF) have been shown to exert beneficial effects on cartilage tissue. Nowadays, differentiated human mesenchymal stem cells (hMSCs) are discussed as an alternative approach for cartilage repair. Therefore, the aim of this study was to examine the impact of EMF on hMSCs during