In-advance trans-medullary stimulation of bone marrow enhances spontaneous repair of full-thickness articular cartilage defects in rabbits

被引:0
作者
Kazuya Nishizawa
Shinji Imai
Tomohiro Mimura
Mitsuhiko Kubo
Susumu Araki
Suguru Shioji
Yoshinori Takemura
Yoshitaka Matsusue
机构
[1] Shiga University of Medical Science,Department of Orthopaedic Surgery
来源
Cell and Tissue Research | 2010年 / 341卷
关键词
In-advance trans-medullary stimulation; Mesenchymal stromal cells; Articular cartilage; Basic fibroblast growth factor; Rabbit;
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摘要
Mesenchymal stromal cells (MSCs), especially those lying close to cartilage defects, are an important cell source for cartilage regeneration. We hypothesize that a larger number of MSCs might become available, if the bone marrow in the immediate vicinity of the subchondral bone is stimulated for MSCs in advance of the creation of cartilage defects. A trans-medullary passage-way reaching the immediate vicinity of the subchondral bone was created 4 days prior to the creation of cartilage defects. In another setting, basic fibroblast growth factor (bFGF) was administered through the trans-medullary passage-way in order to augment the stimulation of MSCs. The rabbits were killed at various times after the creation of cartilage defects. Triple staining of bromodeoxyuridine (BrdU), CD44 and CD45 and histological evaluation were subsequently performed. A considerable proportion of the proliferating cells were identified as bone-marrow-derived MSCs. Enumeration of BrdU-positive cells demonstrated that trans-medullary stimulation, especially with bFGF, increased the number of proliferating cells. The histological grading score of trans-medullary stimulation with bFGF group was superior to that of the other groups. Thus, in-advance stimulation of the bone marrow effectively increases the number of proliferating cells. The putative progenitor cells for chondrocytes stimulated thereby are likely to be recruited to the osteochondral defects at the appropriate time, contributing to the repair of full-thickness articular cartilage defects at the early follow-up time point.
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页码:371 / 379
页数:8
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共 197 条
[1]  
Acharya P(2008)Fibroblast migration is mediated by CD44-dependent TGF beta activation J Cell Sci 121 1393-1402
[2]  
Majumdar S(1990)Ki-67 monoclonal antibody (MAb) reacts with a proliferation associated nuclear antigen in the rabbit Histochemistry 94 201-204
[3]  
Jacob M(1994)Treatment of deep cartilage defects in the knee with autologous chondrocyte transplantation N Engl J Med 331 889-895
[4]  
Hayden J(2002)Articular cartilage injuries Clin Orthop Relat Res 402 21-37
[5]  
Mrass P(1998)Articular cartilage repair and transplantation Arthritis Rheum 41 1331-1342
[6]  
Weninger W(2001)Mesenchymal stem cells: building blocks for molecular medicine in the 21st century Trends Mol Med 7 259-264
[7]  
Assoian R(1972)The repair of large osteochondral defects. An experimental study in horses Clin Orthop Relat Res 82 253-262
[8]  
Puré E(1988)Basic fibroblast growth factor (FGF) promotes cartilage repair in vivo Biochem Biophys Res Commun 156 611-618
[9]  
Apte S(2006)Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement Cytotherapy 8 315-317
[10]  
Brittberg M(1989)Growth-promoting effects of acidic and basic fibroblast growth factor on rabbit articular chondrocytes aging in culture Exp Cell Res 183 388-398