Disruption of the thrombospondin-2 gene alters the lamellar morphology but does not permit vascularization of the adult mouse lumbar disc
© Gruber et al.; licensee BioMed Central Ltd. 2008
Received: 22 May 2008
Accepted: 21 August 2008
Published: 21 August 2008
The biological basis for the avascular state of the intervertebral disc is not well understood. Previous work has suggested that the presence of thrombospondin-1 (TSP-1), a matricellular protein, in the outer annulus reflects a role for this protein in conferring an avascular status to the disc. In the present study we have examined thrombospondin-2 (TSP-2), a matricellular protein with recognized anti-angiogenic activity in vivo and in vitro.
We examined both the location and expression of TSP-2 in the human disc, and its location in the disc and bordering soft tissues of 5-month-old normal wild-type (WT) mice and of mice with a targeted disruption of the TSP-2 gene. Immunohistochemistry and quantitative histology were utilized in this study.
TSP-2 was found to be present in some, but not all, annulus cells of the human annulus and the mouse annulus. Although there was no difference in the number of disc cells in the annulus of TSP-2-null mice compared with that of WT animals, polarized light microscopy revealed a more irregular lamellar collagen structure in null mouse discs compared with WT mouse discs. Additionally, vascular beds at the margins of discs of TSP-2-null mice were substantially more irregular than those of WT animals. Counts of platelet endothelial cell adhesion molecule-1-positive blood vessels in the tissue margin bordering the ventral annulus showed a significantly larger vascular bed in the tissue bordering the disc of TSP-2-null mice compared with that of WT mice (P = 0.0002). There was, however, no vascular ingrowth into discs of the TSP-2-null mice.
These data confirm a role for TSP-2 in the morphology of the disc and suggest the presence of other inhibitors of angiogenesis in the disc. We have shown that although an increase in vasculature was present in the TSP-2-null tissue in the margin of the disc, vascular ingrowth into the body of the disc did not occur. Our results point to the need for future research to understand the transition from the well-vascularized status of the fetal and young discs to the avascular state of the adult human disc or the small mammalian disc.
The thrombospondins (TSPs) are multifunctional matricellular proteins; TSP-1 and TSP-2 have strong anti-angiogenic properties, are present in a number of tissues where they bind to the extracellular matrix (ECM) and, in turn, are themselves able to bind receptors, enzymes, cytokines, proteases, and other ECM proteins [1–6]. TSP-1 and TSP-2 bind matrix metalloproteinase-2, and thereby act to clear this matrix metalloproteinase from the pericellular ECM . Both TSP-1 and TSP-2 function in the cellular response to injury, but only TSP-1 is capable of activating the small latent transforming growth factor beta complex [7, 8].
Previous studies have shown that mice with a disruption of the TSP-2 gene exhibit disordered collagen fibrillogenesis, fragile skin, ligament and tendon laxity, and increased vascularity . Recent work has also shown that the TSP-2-null mouse has a reduction in tissue transglutaminase, an enzyme that acts to introduce covalent intermolecular cross-links in collagen and other proteins; this finding accounts in part for the matrix abnormalities seen in the TSP-2-null mouse, such as fragile skin and lax ligaments . TSP-2-null mice also exhibit significantly greater vascularity in adult and embryonic adipose tissue, and in adult and neonatal dermis .
Bone studies have shown that TSP-2-null mice have increased cortical density in long bones, and a mid-diaphyseal endosteal bone formation rate that is increased compared with that of wild-type (WT) mice . TSP-2-null mice also exhibit an elevated bone formation rate (compared with that of WT mice) following mechanical loading .
TSP-1 is present in the outer annulus of both human and sand rat discs and, at apparently lower levels, in the inner annulus . This work is suggestive of a role for TSP-1 in the avascular status of the disc .
The biological basis for the avascular state of the human adult disc is not well understood, but this question is important because the resulting lowered nutritive state of the disc might be a factor in disc degeneration . Nutrients are believed to reach cells within the disc predominantly through the vertebral endplate, and disc cells are kept viable by nutrients moving by diffusion through the disc matrix.
Several recent studies have utilized murine cervical, lumbar or tail discs as experimental models. The reader is referred to recent reports that provide useful histologic data [13–16] or biomechanical data  on the age-related changes in the normal mouse disc.
The objective of the present work was to examine mice with a targeted disruption of the TSP-2 gene to determine whether mice lacking TSP-2 would show enhanced vascularity of the adult annulus. We first determined the immunolocalization of TSP-2 in the human disc and the normal mouse disc, and subsequently examined mice with a targeted disruption of the TSP-2 gene with respect to the morphology and cellularity of the annulus, the presence of vascular beds within the disc, and vascularity of the soft tissue margin of the disc that serves to supply nutrition to the disc via diffusion. Our studies confirm the expression of TSP-2 in both the human annulus and the WT mouse annulus, but show no vascular ingrowth into the discs of TSP-2-null mice.
Materials and methods
Clinical study population
The experimental study of disc specimens was approved prospectively by the authors' Human Subjects Institutional Review Board at Carolinas Medical Center. The need for informed consent was waived since disc tissue was removed as part of routine surgical practice. The Thompson grading system is used to score disc degeneration over the spectrum of stages from a healthy disc (Thompson grade I) to discs with advanced degeneration (Thompson grade V) .
Patient specimens were derived from surgical disc procedures performed on individuals with herniated discs and degenerative disc disease. Surgical specimens were transported to the laboratory in sterile tissue culture medium, less than 30 minutes after surgical removal, and were placed in 10% neutral buffered formalin for no longer than 24 hours. Care was taken to remove all granulation tissue and to sample only disc tissue. Nonsurgical control donor disc specimens were obtained via the National Cancer Institute Cooperative Human Tissue Network; the specimens were shipped overnight to the laboratory in sterile tissue culture medium and were processed as described below. Specimen procurement from the Cooperative Human Tissue Network was included in our approved protocol by our human subjects Institutional Review board.
Human disc tissues were processed undecalcified and embedded in paraffin, and were processed for immunohistochemistry as described below.
TSP-2 immunolocalization in human disc specimens
Four specimens of human disc tissue were utilized for localization of TSP-2 with immunocytochemistry: a surgical specimen from a 16-year-old female, L3 to L4 (Thompson grade II); a surgical specimen from a 42-year-old female, C5 to C6 (Thompson grade III); a Cooperative Human Tissue Network specimen from a 40-year-old male (Thompson grade II); and a Cooperative Human Tissue Network specimen from L5 to S1 from a 33-year-old female, L3 to L4 (Thompson grade IV).
Gene expression studies in human disc cells
Human disc tissue, annulus cells in monolayer, and annulus cells in three-dimensional culture were assayed for gene expression using the Affymetrix microarray system (Affymetrix, Santa Clara, CA 95051, USA). Cells from the annulus were examined from four subjects: a 52-year-old female, Thompson grade III; a 63-year-old male, Thompson grade IV; a 65-year-old female, Thompson grade IV; and a 33-year-old female control donor, Thompson grade III.
Disc tissue was studied using laser capture microdissection to harvest cells, followed by microarray analysis as previously described . Cultured cells were placed in Extraction Buffer from the PicoPure RNA Isolation Kit (Arcturus, Mountainview, CA, USA). Total RNA was extracted from the tissue according to instructions in the PicoPure RNA Isolation Kit, reverse-transcribed to double-stranded cDNA, subjected to two rounds of transcription, and hybridized to the DNA microarray in the Affymetrix Fluidics Station 400. Affymetrix human U133 X3P arrays were used. The GCOS Affymetrix GeneChip Operating System (version 1.2) was used to determine gene expression levels for TSP-2 (NM_003247.1).
Animal studies were performed after approval by the Institutional Animal Care and Use Committee at the University of Washington. The WT control mice and the TSP-2-null mice studied here have been described previously .
Light microscopy studies of disc tissues
Light microscopy was performed on the lumbar and thoracic spines of four WT mice and four TSP-2-null mice, aged 5 months. Specimens were fixed in either 10% neutral buffered formalin or 70% ethanol, and were decalcified in a solution of 22.5% formic acid (Allegiance, McGraw Park, IL, USA) and 10% sodium citrate (Sigma, St Louis, MO, USA). Complete decalcification was determined by radiography. The spine was cut in sagittal section, embedded in paraffin, and sectioned at 4 μm. Sections were stained with Masson-trichrome stain for the evaluation of general disc features, for polarized light microscopy, and for cell counts.
TSP-1 and TSP-2 in the mouse disc
TSP-1 was identified in the mouse disc with an antibody that recognizes primarily TSP-1 (AB-4, Clone A6.1; LabVision Corporation, Freemont, CA, USA) at a concentration of 8 μg/ml, as previously described . The negative control used with each experiment was mouse IgG1 (Dako-Cytomation, Carpinteria, CA, USA) used at the same concentration. Positive controls (skin and breast tissue) were also included.
Immunolocalization of TSP-2 was performed with an anti-TSP-2 antibody specific for TSP-2, as previously described , with antigen retrieval. Antigen retrieval was performed using Dako Target Retrieval Solution, pH 6.0, for 20 minutes at 95°C, followed by cooling for 20 minutes. Negative controls were processed in the absence of the primary antibody.
Scoring of PECAM-1-positive blood vessels
Platelet endothelial cell adhesion molecule-1 (PECAM-1) was identified as follows: sections were deparaffinized in xylene (Allegiance) and were rehydrated through graded concentrations of alcohol (AAPER, Shelbyville, KY, USA) to distilled water. As shown previously, antigen retrieval methods were required ; antigen retrieval was performed using Dako Target Retrieval Solution, pH 6.0, for 20 minutes at 95°C, followed by cooling for 20 minutes. Endogenous peroxidase was blocked with 3% H2O2 (Sigma). Slides were incubated overnight at 4°C with anti-PECAM-1 IgG (Santa Cruz Biotechnology, Santa Cruz, CA, USA) at a 1:100 dilution. Goat IgG (Vector Laboratories, Burlingame, CA, USA) was used as a negative control. The secondary antibody was biotinylated rabbit anti-goat IgG (Vector) applied for 20 minutes, followed by peroxidase-conjugated streptavidin (Dako) for 10 min and Vector NovaRed (Vector) for 5 minutes. Slides were rinsed in water, counterstained with light green (Polysciences, Warrington, PA, USA), dehydrated, cleared, and mounted with resinous mounting media. Control tissues included mouse spleen and human tonsil.
The number of PECAM-1-positive vascular structures in 40× magnification fields was scored along the border of the ventral disc margin. Only tissue bordering the disc (not including adjacent end plates) was scored. The margins of 20 discs for WT mice and of 15 discs for TSP-2-null mice were evaluated.
Histomorphometry was performed on the annulus of lumbar discs to determine cell densities in WT mice and TSP-null mice. Quantitative histomorphometry was performed on tissue sections stained with Masson-trichrome dye using the OsteoMeasure system (OsteoMetrics, Atlanta, GA, USA).
Standard statistical methods employed SAS software (version 9.1; SAS Institute, Cary, NC, USA), and GraphPad InStat® (version 3.06; GraphPad Inc., San Diego, CA, USA). P < 0.05 was considered statistically significant. Analyses performed included calculation of descriptive statistics and the Wilcoxon rank sum test, which was utilized to assess data from counts of PECAM-positive blood vessels in the soft tissue of the disc margins. Data are expressed as the mean ± standard error of the mean (number).
TSP-2 and its gene expression in human discs
TSP in the mouse lumbar disc
Annulus cell numbers in lumbar discs of WT mice and TSP-2-null mice
Morphology of collagen in discs of WT mice and TSP-2-null mice
Peripheral vascularity around lumbar discs of WT mice and TSP-2-null mice
TSP-2 in the disc
TSP-2, a matricellular protein with recognized anti-angiogenic activity in vivo and in vitro, was found to be present in some, but not all, cells of the human and mouse annulus. Microarray analysis also verified expression of TSP-2 in the human annulus.
It is interesting that the response to a lack of TSP-2 expression in null mice was insufficient to produce vascular ingrowth into the disc. The disc may indeed be unusual in this regard, since surrounding soft tissues bordering the disc displayed the expected increased vascular bed previously seen in soft tissues of the TSP-2-null animal . The annulus contains TSP-2, but apparently does not rely solely upon it to inhibit blood vessel growth; TSP-2 may therefore not participate in regression of neonatal vessels in the disc.
Morphology of the annulus in the TSP-2-null mouse
Although there was no difference in the number of disc cells in the annulus of TSP-2-null mice versus WT animals, an important finding in the present study is the irregular, uneven collagen lamellar structure seen by polarized light microscopy in null mouse discs versus WT mouse discs. Appropriate annular morphology and integrity are essential to the function of the intervertebral disc, and cells in the outer annulus are polarized for directed secretion of ECM components . Ultimately it is the ECM that undergoes failure with disc degeneration; dehydration and matrix fraying culminate in tears within the annulus during biomechanical loading and torsion. Nucleus pulposus and annulus material rupture through these tears, and impinge on nerves, thus causing pain.
Kyriakides and colleagues found that dermal collagen fibers were disorganized in the TSP-2-null mouse, and that the skin of these mice displayed decreased tensile strength . These authors hypothesized that TSP-2 might function as a collagen fibril-associated protein that participates in the regulation of collagen fibril diameter and fibrillogenesis. This hypothesis suggests another avenue to be explored in disc cell biology. Other possibilities include the ability of TSP-2 to regulate the activity of matrix metalloproteinase-2  and tissue transglutaminase . Additional studies of the disc characteristics of the TSP-2-null mouse are needed to determine whether there are ultrastructural changes in collagen fibers similar to those seen in the tendons of TSP-2-null mice (that is, increased numbers of large-diameter fibrils) and to determine whether there is decreased tensile strength in TSP-2-null discs.
Vascular changes in soft tissue bordering the disc in the TSP-2-null mouse
Although there is a rich vascular supply to the developing and newborn disc, vascularity decreases with maturity, and the adult human disc is avascular. This condition is also present in many other species, including the sand rat, a small rodent model of spontaneous, age-related disc degeneration [25, 26].
The small vascular beds along the dorsal and ventral annular surfaces, and vascularization of the vertebral endplate, constitute the main accesses to vasculature for the disc, and nutrients subsequently reach the cells of the disc via diffusion through the disc ECM. In humans and in some animals, including the sand rat, the endplate undergoes calcification with increasing age, and access to nutrients thus decreases further [26–31].
Previous work has shown that the majority of cells in the outer annulus of the human disc and the sand rat disc contain TSP-1. Since TSP-2 has established anti-angiogenic properties, we hypothesized that this matricellular protein might contribute to the avascular state of the disc by its capacity to inhibit vascular ingrowth along the disc margin. One objective of this work was to examine mice with a targeted disruption of the TSP-2 gene to determine whether mice lacking TSP-2 would show enhanced vascularity of the adult annulus. Our studies show that, even in the absence of expression of the TSP-2 gene, vascular ingrowth into the body of the disc did not occur.
The results of the quantitative assessment of the vascular bed in soft tissue along the disc margins that we presented here are similar to those previously published by Kyriakides and colleagues, who counted blood vessels in adipose, dermis, and thymic tissues of WT mice and TSP-2-null mice . A similar increase in vasculature was therefore seen in the TSP-2-null mouse tissue in the margin of the disc. It is interesting to note that the previous investigators also showed that the differences seen in neonatal or embryonic dermis were not as great as those in adult tissue.
In the TSP-2-null specimens examined here, the expected increased vascular bed was present in the soft tissue margin adjacent to the disc. Although we have not measured any nutrient diffusion rates in these discs, we note that this increased adjacent vascularity may potentially result in an increased availability of nutrients to the disc.
It is also of interest to comment on the question of potential compensation between the two TSPs. There is no evidence to date for compensation. Although we have not tested whether upregulation of TSP1 might contribute to the lack of vascularization of the annulus in TSP-2-null mice, the evidence in the literature suggests that compensation by either of the two TSPs does not occur .
Angiogenesis is seen in herniated disc tissue, and basic fibroblast growth factor has been noted in at least some of the blood vessels in the prolapsed disc. In contrast, no immunoreactivity for fibroblast growth factor was seen in intact, nonherniated discs . Vascular endothelial growth factor and platelet-derived growth factor have also been identified in herniated disc tissue [34–37].
There is a complex biological relationship between the intact disc matrix and cells, and the nearby vasculature outside the disc. We now recognize a number of inhibitors of angiogenesis, as discussed in several reviews [38–42]. There are angiogenesis inhibitors that function by inhibition of one, or more than one, angiogenic protein. Endogenous anti-angiogenic proteins have a number of interesting properties ; some can specifically target newly-formed vasculature, but not older blood vessels. Relevant to the disc, tissue inhibitor of metalloproteinase-1 and ECM fragments, including those from collagen, merit further study of their anti-angiogenic potential. Also relevant to the disc are the findings that aggrecan may act in an anti-angiogenic factor , as may other matrix proteoglycan components .
Chondromodulin-I, which is present in the disc , also acts as an endothelial cell growth inhibitor in fetal bovine cartilage, in growth plates, and in embryonic cartilaginous sites. In addition to TSPs, this matrix protein might exert an anti-angiogenic influence in the TSP-2-null mouse discs studied here. The work presented here points to the importance of additional studies of TSP-1-null mice and TSP-2-null mice. In addition, future studies of anti-angiogenic factors in the disc are needed to understand the change from the well-vascularized status of the fetal and young discs to the avascular adult human disc or small mammalian disc.
There is a complex biological relationship between the intact disc matrix and cells and the nearby vasculature outside the disc. We have shown that although an increase in vasculature was present in the TSP-2-null tissue in the margin of the disc, vascular ingrowth into the body of the disc did not occur. The present study also identified a change in lamellar collagen structure in the annulus of the TSP-2-null mouse disc. Our results point to the need for future research to understand the transition from the well-vascularized status of the fetal and young discs to the avascular state of the adult human or small mammalian disc.
= extracellular matrix
= platelet endothelial cell adhesion molecule-1
= wild type.
Supported in part by National Institutes of Health grant AR-45418 (to PB) and grant GM40711 (to EHS).
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