2002
DOI: 10.1016/s0142-9612(01)00086-2
|View full text |Cite
|
Sign up to set email alerts
|

Fluorescently labeled mesenchymal stem cells (MSCs) maintain multilineage potential and can be detected following implantation into articular cartilage defects

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

1
68
0
4

Year Published

2006
2006
2019
2019

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 115 publications
(79 citation statements)
references
References 34 publications
1
68
0
4
Order By: Relevance
“…40 The chondrocytes were also detected in the defect up to 14 weeks after ACI using fluorescent dye. 41 Emans et al 42 demonstrated transplantation of chondrocyte or periosteal cell=scaffold constructs into an osteochondral defect and examined cell viability by fluorescent labeling 5 days after transplantation.…”
Section: Discussionmentioning
confidence: 99%
“…40 The chondrocytes were also detected in the defect up to 14 weeks after ACI using fluorescent dye. 41 Emans et al 42 demonstrated transplantation of chondrocyte or periosteal cell=scaffold constructs into an osteochondral defect and examined cell viability by fluorescent labeling 5 days after transplantation.…”
Section: Discussionmentioning
confidence: 99%
“…The later, identified as marrow stromal cells or mesenchymal stem cells (MSCs), not only support hematopoiesis but also differentiate along various mesodermal lineages to generate osteoblasts, chondrocytes, and adipocytes. [1][2][3] Because of these properties, MSCs have been exploited for their potential to repair or regenerate damaged tissues of mesenchymal origin, including bone fracture healing, 4 tendon repair, 5 cartilage regeneration, 6,7 and support of engraftment after chemotherapy. 8 One group has also identified a subpopulation of bone marrowderived cells, termed multipotent adult progenitor cells (MAPCs), which possess longer proliferative capacity and broader differentiation potential than MSCs, 9,10 including cells of all 3 germ layers in vitro, as well as the ability to generate chimeric mice when injected into blastocysts.…”
Section: Introductionmentioning
confidence: 99%
“…MSCs can be extracted from several organs, such as fetal liver, umbilical cord blood, bone marrow, placenta, adipose tissue, muscle, and dermis (Kraemer 1995), and can be induced to differentiate into cells of the articular cartilage Liechty et al 2000;Toma et al 2002) or chondrocyte lineages (Im et al 2001;Quintavalla et al 2002;Wakitani et al 1994). Furthermore, as IVD cells have phenotypes similar to those of chondrocytes, it would appear that IVD cells are differentiated from MSCs (Risbud et al 2004).…”
Section: Introductionmentioning
confidence: 99%