Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 13 de 13
Filter
Add more filters










Publication year range
1.
Osteoarthritis Cartilage ; 16(1): 70-82, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17644010

ABSTRACT

OBJECTIVE: Articular cartilage is separated from subchondral bone by the tidemark and a calcified cartilage zone. Advancement of the calcified region and tidemark duplication are both hallmarks of osteoarthritis (OA). Currently the mechanisms controlling post-natal articular cartilage mineralization are poorly understood. The objective of this study is to test the hypothesis that cellular communication between different cartilage layers regulates articular chondrocyte mineralization. DESIGN: Co-culture models were established to evaluate the interaction of chondrocytes derived from the surface, middle and deep zones of articular cartilage. The cultures were stimulated with triiodothyronine (T3) to promote chondrocyte hypertrophy. The effects of zonal chondrocyte interactions on chondrocyte mineralization were examined over time. RESULTS: Co-culture of deep zone chondrocytes (DZCs) with surface zone chondrocytes (SZCs) suppressed the T3-induced increase in alkaline phosphatase (ALP) activity and related mineralization. Moreover, SZC-DZC co-culture was associated with a significantly higher parathyroid hormone-related peptide (PTHrP) expression when compared to controls. When PTHrP(1-40) was added to the DZC-only culture, it suppressed DZC ALP activity similar to the inhibition observed in co-culture with SZC. In addition, treatment with PTHrP reversed the effect of T3 stimulation on the expression of hypertrophic markers (Indian hedgehog, ALP, matrix metalloproteinases-13, Type X collagen) in the DZC cultures. Moreover, blocking the action of PTHrP significantly increased ALP activity in SZC+DZC co-culture. CONCLUSION: Our findings demonstrate the role of zonal chondrocyte interactions in regulating cell mineralization and provide a plausible mechanism for the post-natal regulation of articular cartilage matrix organization. These findings also have significant implications in understanding the pathology of articular cartilage as well as devising strategies for functional cartilage repair.


Subject(s)
Alkaline Phosphatase/metabolism , Cartilage, Articular/drug effects , Chondrocytes/drug effects , Parathyroid Hormone-Related Protein/pharmacology , Triiodothyronine/pharmacology , Animals , Cartilage, Articular/metabolism , Cattle , Chondrocytes/metabolism , Coculture Techniques , Collagen Type X/metabolism , Hedgehog Proteins/metabolism , Matrix Metalloproteinase 13/metabolism , Parathyroid Hormone-Related Protein/metabolism
2.
J Bone Joint Surg Br ; 89(5): 672-85, 2007 May.
Article in English | MEDLINE | ID: mdl-17540757

ABSTRACT

Gene therapy with insulin-like growth factor-1 (IGF-1) increases matrix production and enhances chondrocyte proliferation and survival in vitro. The purpose of this study was to determine whether arthroscopically-grafted chondrocytes genetically modified by an adenovirus vector encoding equine IGF-1 (AdIGF-1) would have a beneficial effect on cartilage healing in an equine femoropatellar joint model. A total of 16 horses underwent arthroscopic repair of a single 15 mm cartilage defect in each femoropatellar joint. One joint received 2 x 10(7) AdIGF-1 modified chondrocytes and the contralateral joint received 2 x 10(7) naive (unmodified) chondrocytes. Repairs were analysed at four weeks, nine weeks and eight months after surgery. Morphological and histological appearance, IGF-1 and collagen type II gene expression (polymerase chain reaction, in situ hybridisation and immunohistochemistry), collagen type II content (cyanogen bromide and sodium dodecyl sulphate-polyacrylamide gel electrophoresis), proteoglycan content (dimethylmethylene blue assay), and gene expression for collagen type I, matrix metalloproteinase (MMP)-1, MMP-3, MMP-13, aggrecanase-1, tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) and TIMP-3 were evaluated. Genetic modification of chondrocytes significantly increased IGF-1 mRNA and ligand production in repair tissue for up to nine weeks following transplantation. The gross and histological appearance of IGF-1 modified repair tissue was improved over control defects. Gross filling of defects was significantly improved at four weeks, and a more hyaline-like tissue covered the lesions at eight months. Histological outcome at four and nine weeks post-transplantation revealed greater tissue filling of defects transplanted with genetically modified chondrocytes, whereas repair tissue in control defects was thin and irregular and more fibrous. Collagen type II expression in IGF-1 gene-transduced defects was increased 100-fold at four weeks and correlated with increased collagen type II immunoreaction up to eight months. Genetic modification of chondrocytes with AdIGF-1 prior to transplantation improved early (four to nine weeks), and to a lesser degree long-term, cartilage healing in the equine model. The equine model of cartilage healing closely resembles human clinical cartilage repair. The results of this study suggest that cartilage healing can be enhanced through genetic modification of chondrocytes prior to transplantation.


Subject(s)
Cartilage, Articular/injuries , Chondrocytes/transplantation , Genetic Therapy/methods , Insulin-Like Growth Factor I/biosynthesis , Wound Healing , Adenoviridae/genetics , Animals , Arthroscopy , Cartilage, Articular/metabolism , Cartilage, Articular/pathology , Cartilage, Articular/surgery , Chondrocytes/metabolism , Collagen Type II/biosynthesis , Collagen Type II/genetics , Disease Models, Animal , Female , Gene Expression , Genetic Vectors , Horses , Insulin-Like Growth Factor I/genetics , Insulin-Like Growth Factor I/physiology , Male , Proteoglycans/metabolism , RNA, Messenger/genetics , Transduction, Genetic
3.
Tissue Antigens ; 66(6): 674-82, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16305684

ABSTRACT

The hereditary conservation in the genetically encoded CD1D sequences of various primates was analyzed. Genomic CD1D sequences of 17 rhesus macaques with distinct origins, eight Indian and nine Chinese, were examined and differences of only one or two nucleotides were detected and the consensus sequence of rhesus CD1D was determined. CD1D consensus sequences of three African green monkeys (AGMs) and the rhesus monkeys were then compared to study the evolutionary differences among interspecies. The CD1D consensus sequence determined from AGMs apparently differed by seven nucleotides from the rhesus consensus sequence, and nucleotide difference induced only three amino acid changes within Exon3, corresponding to the alpha2 domain of CD1d having a hydrophobic ligand-binding pocket. Such changes in the alpha2 domain may alter the characteristics of the SIV-derived glycolipid/lipid antigens presented by each CD1d molecule to innate natural killer T cells. In addition, the CD1D genomic sequences of three chimpanzees (chimps) were determined. To our surprise, although Exon2 and Exon3 reflecting antigen-binding alpha1 and alpha2 domains in chimps' CD1D were identical to that in humans except one amino acid, three amino acids within Exon4, reflecting alpha3 domain, were distinct from humans, and one of them was identical to those in rhesus and AGM CD1D. On the basis of the findings, the evolutionary relationship of the CD1d molecules among the various primates and their HIV-1/SIV susceptibility will be discussed.


Subject(s)
Antigens, CD1/genetics , Chlorocebus aethiops/genetics , Dendritic Cells/immunology , Evolution, Molecular , Macaca mulatta/genetics , Amino Acid Sequence , Animals , Antigens, CD1d , Base Sequence , Conserved Sequence , DNA/genetics , Humans , Molecular Sequence Data , Sequence Homology, Amino Acid , Sequence Homology, Nucleic Acid , Species Specificity
4.
J Orthop Res ; 19(5): 751-8, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11562118

ABSTRACT

Bone morphogenic protein-7 (BMP-7) supports ectopic cartilage and bone formation, is expressed in normal articular cartilage, and increases matrix synthesis in chondrocytes. Based on this knowledge, we hypothesized that an adenovirus (Ad) vector encoding human BMP-7 could be used to modify chondrocytes genetically to improve their capacity for cartilage repair. An adenovirus vector encoding BMP-7 (AdBMP-7) was constructed and its bioactivity confirmed by ectopic bone formation assay. AdBMP-7 modification of bovine chondrocytes induced expression of BMP-7 mRNA and bioactive protein, resulting in an increase in incorporation of 35SO4- into proteoglycan, 3H-proline uptake into protein, and the expression of the cartilage-specific matrix genes, aggrecan and type II collagen. An in vitro model of chondrocyte transplantation was used to demonstrate the feasibility of using genetically modified chondrocytes to enhance formation of cartilage-like tissue. When transplanted onto cartilage explants and maintained in vitro for 3 weeks, chondrocytes modified with AdBMP-7 formed 1.9-fold thicker tissue than chondrocytes modified with a control vector (P < 0.001). This tissue was positive for type II collagen and proteoglycan but negative for type X collagen and demonstrated a cartilage-like morphology. These observations suggest that Ad-mediated transfer of BMP-7 gene to chondrocytes enhances the chondrocyte-specific matrix synthesis and their capacity to form cartilage-like tissue, thus representing a strategy that may improve cell-based cartilage repair.


Subject(s)
Bone Morphogenetic Proteins/genetics , Cartilage, Articular/cytology , Chondrocytes/physiology , Extracellular Matrix Proteins/genetics , Extracellular Matrix/metabolism , Transforming Growth Factor beta , Adenoviridae/genetics , Aggrecans , Animals , Bone Morphogenetic Protein 7 , Bone Morphogenetic Proteins/metabolism , Cartilage, Articular/physiology , Cattle , Chondrocytes/cytology , Chondrocytes/transplantation , Collagen/genetics , Gene Expression/physiology , Genetic Vectors , In Vitro Techniques , Lectins, C-Type , Proteoglycans/genetics , RNA, Messenger/analysis
6.
Orthop Clin North Am ; 31(3): 473-84, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10882472

ABSTRACT

Gene therapy is a novel therapeutic modality for repair and regeneration of musculoskeletal tissues, including the spine. Various methods for therapeutic gene transfer are presented in this article. Several studies in which gene transfer has been used specifically to enhance spine fusion in animal models are reviewed.


Subject(s)
Genetic Therapy/methods , Spinal Fusion/methods , Transforming Growth Factor beta , Adaptor Proteins, Signal Transducing , Animals , Bone Morphogenetic Protein 2 , Bone Morphogenetic Proteins/genetics , Carrier Proteins/genetics , Cytoskeletal Proteins , Disease Models, Animal , Gene Transfer Techniques , Humans , Intracellular Signaling Peptides and Proteins , LIM Domain Proteins
7.
J Clin Invest ; 103(4): 579-87, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10021467

ABSTRACT

Primary fibroblasts are not efficiently transduced by subgroup C adenovirus (Ad) vectors because they express low levels of the high-affinity Coxsackie virus and adenovirus receptor (CAR). In the present study, we have used primary human dermal fibroblasts as a model to explore strategies by which Ad vectors can be designed to enter cells deficient in CAR. Using an Ad vector expressing the human CAR cDNA (AdCAR) at high multiplicity of infection, primary fibroblasts were converted from being CAR deficient to CAR sufficient. Efficiency of subsequent gene transfer by standard Ad5-based vectors and Ad5-based vectors with alterations in penton and fiber was evaluated. Marked enhancement of binding and transgene expression by standard Ad5 vectors was achieved in CAR-sufficient fibroblasts. Expression by AdDeltaRGDbetagal, an Ad5-based vector lacking the arginine-glycine-aspartate (RGD) alphaV integrin recognition site from its penton base, was achieved in CAR-sufficient, but not CAR-deficient, cells. Fiber-altered Ad5-based vectors, including (a) AdF(pK7)betagal (bearing seven lysines on the end of fiber) (b) AdF(RGD)betagal (bearing a high-affinity RGD sequence on the end of fiber), and (c) AdF9sK betagal (bearing a short fiber and Ad9 knob), demonstrated enhanced gene transfer in CAR-deficient fibroblasts, with no further enhancement in CAR-sufficient fibroblasts. Together, these observations demonstrate that CAR deficiency on Ad targets can be circumvented either by supplying CAR or by modifying the Ad fiber to bind to other cell-surface receptors.


Subject(s)
Adenoviruses, Human , Capsid Proteins , Gene Transfer Techniques , Genetic Vectors , Receptors, Virus/metabolism , Adenoviruses, Human/metabolism , Capsid/genetics , Capsid/metabolism , Cells, Cultured , Fibroblasts/cytology , Gene Expression , Humans , Receptors, Virus/genetics , Transgenes , Up-Regulation
8.
Am J Respir Cell Mol Biol ; 20(3): 361-70, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10030833

ABSTRACT

Robust expression of genes transferred by adenovirus (Ad) vectors depends upon efficient entry of vectors into target cells. Cells deficient in the coxsackie/adenovirus receptor (CAR) are difficult targets for Ad-mediated gene transfer. We hypothesized that low levels of CAR expression may be responsible, in part, for the relative inefficiency of Ad-mediated gene transfer to human alveolar macrophages (AMs). CAR gene expression was detected in human AMs by reverse transcription-polymerase chain reaction and at low levels by Northern analysis. Indirect immunofluorescence showed specific, low-intensity surface staining for CAR, but at levels below those found on the positive-control A549 human lung epithelial cell line. Consistent with this, AMs expressed Ad vector transgenes 100 to 1,000-fold less efficiently than A549 cells, as assessed using the beta-galactosidase reporter (chemiluminescence assay) and green fluorescent protein (fluorescence microscopy and flow cytometry). At high multiplicity of infection, AMs from an HIV+ individual could be transduced with an AdIFNgamma vector to secrete detectable human interferon-gamma. Ad transgene expression by AMs was blocked by capsid fiber protein, suggesting that CAR is required in the pathway for productive Ad entry into alveolar macrophages. To confirm that Ad transgene expression by AMs is limited by low levels of CAR expression, cells were infected with an Ad vector containing the CAR complementary DNA (cDNA). Enhanced expression of CAR protein was demonstrated by indirect immunofluorescence, and the CAR cDNA-transduced cells showed 5-fold enhancement of subsequent Ad transgene expression. These observations demonstrate that human AMs can be targets for Ad-mediated gene transfer, but that efficiency of transgene expression is limited, at least in part, by low levels of CAR expression.


Subject(s)
Adenoviridae/genetics , Gene Transfer Techniques , Genetic Vectors , Macrophages, Alveolar/virology , Receptors, Virus/analysis , Coxsackie and Adenovirus Receptor-Like Membrane Protein , Enterovirus , Green Fluorescent Proteins , Humans , Interferon-gamma/genetics , Luminescent Proteins/genetics , RNA, Messenger/analysis , Receptors, Virus/biosynthesis , Receptors, Virus/genetics , beta-Galactosidase/genetics
9.
Arthroscopy ; 14(1): 80-4, 1998.
Article in English | MEDLINE | ID: mdl-9486339

ABSTRACT

Nine patients had combined anterior cruciate ligament (ACL) disruption and patella dislocation and underwent surgical reconstruction of one or both of these injuries. Six patients had both the ACL reconstructed and the patella realigned, and three had only the ACL reconstructed. Associated injuries were present in eight cases; these included meniscal tears in eight patients and medial collateral ligament injuries in two of these same patients. At final follow-up, at an average 19.7 months, examination revealed an average grade 1A Lachman and no pivot on all patients who underwent ACL reconstruction. No patients had hypermobile patellae or apprehension. One patient had a 4 degrees loss of extension and none had a loss of flexion. Two patients had continued anterior knee pain at final follow-up; one of these patients was the same person who had a loss of extension. None had recurrent instability of the ACL and none had recurrent instability of the patella.


Subject(s)
Anterior Cruciate Ligament Injuries , Joint Dislocations/surgery , Patella/injuries , Adolescent , Adult , Anterior Cruciate Ligament/surgery , Female , Follow-Up Studies , Humans , Knee Injuries/complications , Knee Injuries/surgery , Male , Pain/etiology , Patella/surgery , Postoperative Complications , Treatment Outcome
12.
J Bone Joint Surg Am ; 75(12): 1795-803, 1993 Dec.
Article in English | MEDLINE | ID: mdl-8258550

ABSTRACT

Our study evaluated tendon-to-bone healing in a dog model. Twenty adult mongrel dogs had a transplantation of the long digital extensor tendon into a 4.8-millimeter drill-hole in the proximal tibial metaphysis. Four dogs were killed at each of five time-periods (two, four, eight, twelve, and twenty-six weeks after the transplantation), and the histological and biomechanical characteristics of the tendon-bone interface were evaluated. Serial histological analysis revealed progressive reestablishment of collagen-fiber continuity between the bone and the tendon. A layer of cellular, fibrous tissue was noted between the tendon and the bone, along the length of the bone tunnel; this layer progressively matured and reorganized during the healing process. The collagen fibers that attached the tendon to the bone resembled Sharpey fibers. High-resolution radiographs showed remodeling of the trabecular bone that surrounded the tendon. At the two, four, and eight-week time-periods, all specimens had failed by pull-out of the tendon from the bone tunnel. The strength of the interface was noted to have significantly and progressively increased between the second and the twelfth week after the transplantation. At the twelve and twenty-six-week time-periods, all specimens had failed by pull-out of the tendon from the clamp or by mid-substance rupture of the tendon. The progressive increase in strength was correlated with the degree of bone ingrowth, mineralization, and maturation of the healing tissue, noted histologically.


Subject(s)
Bone and Bones/physiology , Bone and Bones/surgery , Tendons/physiology , Tendons/transplantation , Wound Healing , Animals , Biomechanical Phenomena , Bone Remodeling , Bone and Bones/pathology , Dogs , Ligaments/surgery , Tendons/pathology , Wound Healing/physiology
13.
Am J Psychiatry ; 150(5): 813-5, 1993 May.
Article in English | MEDLINE | ID: mdl-8480830

ABSTRACT

Some depressed patients may suffer from restricted central hypothyroidism, which could occur if levels of the thyroid hormone transport protein transthyretin were low. CSF transthyretin was measured in eight inpatients with refractory major depression and nine neurological patients. The depressed patients had significantly lower transthyretin levels than the comparison subjects, suggesting that central hypothyroidism, with normal peripheral thyroid concentrations, could occur in some depressed patients.


Subject(s)
Depressive Disorder/cerebrospinal fluid , Prealbumin/cerebrospinal fluid , Adult , Depressive Disorder/etiology , Female , Hospitalization , Humans , Hypothyroidism/complications , Male , Middle Aged , Nervous System Diseases/cerebrospinal fluid , Pilot Projects
SELECTION OF CITATIONS
SEARCH DETAIL
...