Literature DB >> 17333068

[Use of bone marrow mesenchymal stem cells for ex vivo cartilage regeneration].

S Grässel1, N Ahmed.   

Abstract

Articular cartilage disorders and injuries often result in lifelong chronic pain and compromised quality of life. When it comes to local articular cartilage defects, modern medicine is limited to short-term pain relief and inflammation control. In extreme cases the affected tissue is surgically removed and replaced by a synthetic prosthesis of limited durability. Cell-based therapies to regenerate articular cartilage have been in use since 1994. Such therapies provide a healthy population of cells to the injured site and require differentiated chondrocytes from the uninjured site as base material. Their usage often leads to donor site morbidity and they generate rigid fibrous cartilage where more flexible hyaline cartilage is required. The major restrictive factors for such methods are inadequate number and limited proliferation capacity of chondrocytes in vitro. Tissue engineering of adult marrow stromal cells/mesenchymal stem cells (MSCs) with their almost unlimited proliferation potential and proven capability to differentiate into chondrocytes for ex vivo generation of cartilage tissue still remains a vision. For optimal harnessing of MSCs as chondroprogenitor cells, basic background information regarding commitment to the lineage, cartilage differentiation and the regulatory factors and molecules involved is essential.

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Year:  2007        PMID: 17333068     DOI: 10.1007/s00132-007-1058-7

Source DB:  PubMed          Journal:  Orthopade        ISSN: 0085-4530            Impact factor:   1.087


  42 in total

1.  The splice variants VEGF121 and VEGF189 of the angiogenic peptide vascular endothelial growth factor are expressed in osteoarthritic cartilage.

Authors:  T Pufe; W Petersen; B Tillmann; R Mentlein
Journal:  Arthritis Rheum       Date:  2001-05

2.  The role of vascular endothelial growth factor in human dental pulp cells: induction of chemotaxis, proliferation, and differentiation and activation of the AP-1-dependent signaling pathway.

Authors:  K Matsushita; R Motani; T Sakuta; N Yamaguchi; T Koga; K Matsuo; S Nagaoka; K Abeyama; I Maruyama; M Torii
Journal:  J Dent Res       Date:  2000-08       Impact factor: 6.116

Review 3.  Stem cells and their niches.

Authors:  Kateri A Moore; Ihor R Lemischka
Journal:  Science       Date:  2006-03-31       Impact factor: 47.728

Review 4.  The control of chondrogenesis.

Authors:  Mary B Goldring; Kaneyuki Tsuchimochi; Kosei Ijiri
Journal:  J Cell Biochem       Date:  2006-01-01       Impact factor: 4.429

5.  Cellular activation of proMMP-13 by MT1-MMP depends on the C-terminal domain of MMP-13.

Authors:  Vera Knäuper; Louise Bailey; Joanna R Worley; Paul Soloway; Margaret L Patterson; Gillian Murphy
Journal:  FEBS Lett       Date:  2002-12-04       Impact factor: 4.124

6.  Smad3 induces chondrogenesis through the activation of SOX9 via CREB-binding protein/p300 recruitment.

Authors:  Takayuki Furumatsu; Masanao Tsuda; Noboru Taniguchi; Yoshitaka Tajima; Hiroshi Asahara
Journal:  J Biol Chem       Date:  2004-12-28       Impact factor: 5.157

7.  Biochemical characterization of human collagenase-3.

Authors:  V Knäuper; C López-Otin; B Smith; G Knight; G Murphy
Journal:  J Biol Chem       Date:  1996-01-19       Impact factor: 5.157

8.  Sox9 is required for cartilage formation.

Authors:  W Bi; J M Deng; Z Zhang; R R Behringer; B de Crombrugghe
Journal:  Nat Genet       Date:  1999-05       Impact factor: 38.330

9.  Cloning, expression, and type II collagenolytic activity of matrix metalloproteinase-13 from human osteoarthritic cartilage.

Authors:  P G Mitchell; H A Magna; L M Reeves; L L Lopresti-Morrow; S A Yocum; P J Rosner; K F Geoghegan; J E Hambor
Journal:  J Clin Invest       Date:  1996-02-01       Impact factor: 14.808

10.  Treatment of deep cartilage defects in the knee with autologous chondrocyte transplantation.

Authors:  M Brittberg; A Lindahl; A Nilsson; C Ohlsson; O Isaksson; L Peterson
Journal:  N Engl J Med       Date:  1994-10-06       Impact factor: 91.245

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  1 in total

1.  Transplanted bone marrow stromal cells migrate, differentiate and improve motor function in rats with experimentally induced cerebral stroke.

Authors:  Jeng-Rung Chen; Guang-Yan Cheng; Ching-Chung Sheu; Guo-Fang Tseng; Tsyr-Jiuan Wang; Yong-San Huang
Journal:  J Anat       Date:  2008-07-18       Impact factor: 2.610

  1 in total

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