Skip to main content
  • Research article
  • Open access
  • Published:

Long-term cyclical in vivoloading increases cartilage proteoglycan content in a spatially specific manner: an infrared microspectroscopic imaging and polarized light microscopy study


Understanding the changes in collagen and proteoglycan content of cartilage due to physical forces is necessary for progress in treating joint disorders, including those due to overuse. Physical forces in the chondrocyte environment can affect the cellular processes involved in the biosynthesis of extracellular matrix. In turn, the biomechanical properties of cartilage depend on its collagen and proteoglycan content. To understand changes due to physical forces, this study examined the effect of 80 cumulative hours of in vivo cyclical joint loading on the cartilage content of proteoglycan and collagen in the rabbit metacarpophalangeal joint. The forepaw digits of six anesthetized New Zealand White adult female rabbits were repetitively flexed at 1 Hz with an estimated joint contact pressure of 1 to 2 MPa. Joints were collected from loaded and contralateral control specimens, fixed, decalcified, embedded, and thin-sectioned. Sections were examined under polarized light microscopy to identify and measure superficial and mid zone thicknesses of cartilage. Fourier Transform Infrared microspectroscopy was used to measure proteoglycan and collagen contents in the superficial, mid, and deep zones. Loading led to an increase in proteoglycan in the cartilage of all six rabbits. Specifically, there was a 46% increase in the cartilage deep zone (p = 0.003). The collagen content did not change with loading. Joint loading did not change the superficial and mid zone mean thicknesses. We conclude that long-term (80 cumulative hours) cyclical in vivo joint loading stimulates proteoglycan synthesis. Furthermore, stimulation is localized to cartilage regions of high hydrostatic pressure. These data may be useful in developing interventions to prevent overuse injuries or in developing therapies to improve joint function.


Extracellular matrix composition dictates the mechanical properties of cartilage. Proteoglycan and collagen are two important structural components of the cartilage extracellular matrix [1, 2]. The highly anionic glycosaminoglycan (GAG) component of proteoglycan provides hydration and swelling pressure to the tissue and enables it to resist compressive forces. The difference between the ionic composition of the cartilage matrix and the cartilage interstitial fluid gives rise to the osmotic pressure that is always present in the extracellular matrix, even in cartilage that is unloaded [3]. Specifically, the negative fixed charges on the GAGs control the concentration of mobile ions in cartilage [4]. Because an increase in the concentration of mobile ions increases the hydrostatic pressure of cartilage, there is a direct relation between fixed charged density and the mechanical properties of cartilage, particularly stiffness [5]. Collagen fibrils confine the proteoglycan expansion and provide the extracellular matrix with tensile strength [6, 7].

Cartilage is a non-homogeneous tissue. It can be divided into three distinct zones based on collagen fibril orientation [8]. The superficial zone is characterized with the fibrils aligned tangentially to the surface, the mid zone shows random alignment, whereas the deep zone contains fibrils that are oriented perpendicularly to the surface [9]. The distribution of proteoglycan and collagen varies with depth in different cartilage zones and is responsible for the load-carrying capability of cartilage. Remodeling of cartilage, as well as degradation of proteoglycans and/or the collagen fibrils, not only alters the chemical makeup of cartilage but also changes its mechanical properties. The cellular processes involved can be affected by physical forces in the chondrocyte environment as demonstrated by studies that have examined the biosynthetic response of articular cartilage explants to in vitro loading [1014]. However, the biosynthetic response of cartilage to physiological loading within intact joints is not clear.

To investigate this response, we have developed a rabbit model of in vivo cyclical joint loading [15]. After chronic exposure (80 cumulative hours), loaded joints were prepared as thin sections to evaluate localization of extracellular matrix changes. The thicknesses of specific cartilage zones were measured with polarized light microscopy (PLM), which uses the birefringence of collagen to visualize fiber alignment [9]. Changes in chemical composition in the superficial, mid, and deep zones were examined using Fourier Transform Infrared (FTIR) microspectroscopy. FTIR microspectroscopy is a novel non-destructive method for visualizing the spatial distribution and the amount of chemical constituents in thin tissue sections [16]. Absorption peaks in an infrared spectrum represent a fingerprint of the sample under study. Infrared spectroscopy combined with microscopy can yield molecular information at the microscopic level. Our hypothesis is that physiologic, in vivo cyclical joint loading alters the regional chemical composition of cartilage, specifically proteoglycan.

Materials and methods

Joint loading

A novel in vivo rabbit model of repetitive joint flexion and loading was developed to simulate hand activities associated with the workplace [15]. All procedures received prior approval and oversight from the University of California's Care and Use of Animals Committee and institutional approval. The digits of adult female New Zealand White rabbits (n = 6) were repetitively flexed and loaded. Loading was performed with the rabbits under anesthesia. A Grass-Telefactor stimulator (Grass Technologies, West Warwick, RI, USA) was used to excite the flexor digitorum profundus (FDP) muscle of the experimental limb at 1 Hz, causing the digits to flex. A light-weight finger cuff was attached to the third digit and connected to a load cell. The stimulator voltage was adjusted to achieve an equivalent to 17.5% of the maximum muscle force of this type and size of rabbit (preliminary data, n = 4 rabbits). This stimulation setting resulted in the load cell measurement of 0.42 N peak force at the third digit tip. Applying free-body analysis to our cyclical joint loading protocol, we estimated that the joint contact force is approximately 3 N and the 'nominal' joint contact pressure is between 1 and 2 MPa. Loading was carried out for 80 cumulative hours in 2-hour increments, 3 days a week for 14 weeks. The contra-lateral limb (control) was neither stimulated nor loaded.

Once the loading was completed, the rabbits were euthanized and the metacarpophalangeal (MCP) joints of both limbs were removed, fixed in formalin, decalcified, embedded in paraffin, and sectioned in the sagittal plane. One section (7 μm) from each joint was placed onto an infrared-reflecting microscope slide (MirrIR low-e microscope slides; Kevley Technologies, Chesterland, OH, USA) for FTIR analyses. Three sections from each joint were placed onto Starfrost slides (Fisher Scientific International, Hampton, NH, USA) for PLM.

FTIR analyses

The FTIR data were collected at 16-cm-1 resolution using a mid-infrared Michelson-type step-scan interferometer (ThermoNicolet 870; Thermo Electron Corporation, Waltham, MA, USA) coupled to an ImageMax infrared microscope (Thermo Electron Corporation) with a 64 × 64-pixel mercury cadmium telluride focal plane array detector [17] under N2 purge. All FTIR imaging was carried out at the Musculoskeletal and Quantitative Imaging Research Center, University of California (San Francisco, CA, USA). Information on the amounts and distribution of proteoglycan and collagen was collected in a 200 × 100 μm region of interest (ROI). The 100-μm depth was found previously to cover the entire uncalcified cartilage of the rabbit MCP joint [15]. The FTIR images were baseline-subtracted and background-corrected. A standard paraffin spectrum was subtracted from the spectra to account for any changes in the spectra due to the embedding medium. The paraffin spectrum was collected from a 7-μm-thick section of the same paraffin as used in the embedding medium. The amount of proteoglycan was measured as the mean integrated area of the sugar peak (1,185 - 960 cm-1) in the ROI defined above for each FTIR image [18]. The amount of collagen was measured as the mean integrated area of the amide I peak (1,710 - 1,595 cm-1) in the same ROIs [18]. All FTIR data processing was performed using the Isys software package version 2.1 R1247 (Spectral Dimensions, Inc., Olney, MD, USA).

Polarized light microscopy

Sections on slides for PLM were immersed in xylene for three cycles of 5 minutes each at 20°C to remove paraffin, which interferes with analysis. The sections were unstained and covered with a coverslip using xylene-based mounting medium (Cytoseal; Richard-Allan Scientific, Kalamazoo, MI, USA). Data were collected using a light microscope fitted with polarizers (Axioskop2; Carl Zeiss, Göttingen, Germany) and connected to a digital CCD (charge-coupled device) camera (Axiocam; Carl Zeiss). Specimens were transilluminated by polarized light. A × 20 objective was used for digital image collection. Axiovision software version 3.1 (Carl Zeiss) was used for camera control and digital image collection. During data collection, the joint articular surface for each section was aligned 45° to the polarizer axis to achieve a maximum in light intensity which is dependent upon the angle of the specimen relative to the axis of the cross polarizers. Digital images were captured. The superficial and mid zone mean thicknesses of rabbit MCP cartilage were measured in a 300 × 100 μm ROI positioned on the palmar surface of the metacarpal bone, a location used for previous studies [15]. The superficial and mid zones were outlined manually, and the areas of the zones were measured. The mean thicknesses for the superficial and mid zones were calculated as the area divided by the width.

Proteoglycan distribution

Zonal variation of the amounts of proteoglycan and collagen was determined. Using the data from PLM, thicknesses corresponding to the superficial, mid, and deep zones were assigned to each FTIR dataset. Based on PLM analysis, the superficial zone was designated from the joint surface (at 0 μm) to 8 μm from the joint surface. The mid zone was from 8 to 53 μm, and the deep zone was from 53 to 100 μm [9]. The amounts of proteoglycan and collagen were calculated for each cartilage zone.

Statistical analyses

To identify changes with loading in the biochemical content of cartilage, the outcome measures were mean integrated value of total proteoglycan in the full cartilage thickness and mean integrated value of total collagen in the full cartilage thickness. To identify changes with loading in the zonal thickness, the outcome measures were cartilage superficial zone mean thickness and cartilage mid zone mean thickness. To identify depth-specific changes in proteoglycan due to loading, the outcome measures were mean integrated value of proteoglycan in the superficial zone of cartilage, mean integrated value of proteoglycan in the mid zone of cartilage, and mean integrated value of proteoglycan in the deep zone of cartilage.

Two-tailed, paired Student t tests were used to compare control and loaded specimens (Sigma Plot version 8.1; Systat Software, Inc., Richmond, CA, USA). The statistical significance level alpha (α) was 0.05.


Proteoglycan and collagen content in the total uncalcified cartilage

The amount of proteoglycan increased in the loaded joint compared with the control joint for all six rabbits (Table 1). The mean (± standard deviation [SD]) of integrated proteoglycan peak values of the control joints was 4.4 (± 1.9), which increased to 6.5 (± 2.4) for the loaded joints (p = 0.03). The mean percentage increase in proteoglycan due to loading was 64%; the median was 29.5%. A control rabbit was housed under identical conditions but without FDP stimulation or anesthesia. No difference in the amount of proteoglycan was observed between right and left joints of the limbs of this control rabbit (data not shown).

Table 1 Proteoglycan content in cartilage of cyclically loaded rabbit metacarpophalangeal joints and their contra-lateral controls

Collagen content was also measured using FTIR (Table 2). The mean (± SD) of integrated collagen peak values of the control joints was 35.3 (± 5.3) and for the loaded joints was 33.5 (± 3.8); the difference was not significant (p = 0.20).

Table 2 Collagen content in the cartilage of cyclically loaded rabbit metacarpophalangeal joints and their contra-lateral controls

The amount of proteoglycan in each ROI was normalized to the collagen content (Table 3). The mean (± SD) of normalized proteoglycan of the control joints was 0.12 (± 0.06), which increased to 0.19 (± 0.07) for the loaded joints, a statistically significant difference (p = 0.03). The mean percentage increase in normalized proteoglycan due to loading was 83%; the median was 35%. There was no difference between the right and left limbs of the non-treated control rabbit after normalizing to collagen.

Table 3 Normalized proteoglycan content in the cartilage of cyclically loaded rabbit metacarpophalangeal joints and their contra-lateral controls

Superficial and mid zone thicknesses

The superficial and mid zone thicknesses of rabbit MCP joint cartilage were measured using PLM (Figure 1; Table 4). The mean (± SD) superficial zone thicknesses for the control and loaded joints were 8.11 μm (± 1.2) and 8.3 μm (± 1.7), respectively. The mean (± SD) mid zone thicknesses for the control and loaded joints were 44.03 μm (± 7.9) and 45.72 μm (± 8.2), respectively. There were no statistically significant differences between the thicknesses of the control versus the loaded joints for the superficial (p = 0.77) and mid (p = 0.73) zones.

Figure 1
figure 1

Microscopic images of joint cartilage from region of interest. (a) Rabbit MCP joint sections were stained with iron hematoxylin, safranin O, and fast green. This combination of stains identifies the uncalcified cartilage (red), calcified cartilage (dark red), and bone (blue-green). The tidemark (arrow) is apparent and marks the division between the uncalcified and calcified cartilage. (b) Unstained sections were imaged under polarized light microscopy. The superficial zone is indicated by the two arrows at the articular surface. The bracket encloses the mid zone, which due to the anisotropic arrangement of collagen fibers does not exhibit birefringence. Bars = 100 μm.

Table 4 Zone thicknesses of articular cartilage in cyclically loaded rabbit metacarpophalangeal joints and their contra-lateral controls

Zonal variation of proteoglycan

Mean zone thicknesses were applied to the FTIR maps to measure the zonal variation of proteoglycan (Figure 2). The mean (± SD) of integrated proteoglycan peak values (normalized to collagen content) of the control joints in the superficial zone of cartilage was 0.16 (± 0.09) and was 0.18 (± 0.10) for the loaded joints. The difference between the control and loaded superficial zone proteoglycans was not significant (p = 0.60). In the mid zone, the mean (± SD) of integrated proteoglycan peak values (normalized to collagen content) of the control joints was 0.14 (± 0.06) and 0.20 (± 0.09) for the loaded joints. The difference between the control and loaded mid zone proteoglycan was not significant (p = 0.20).

Figure 2
figure 2

Representative Fourier Transform Infrared maps of proteoglycan in the unloaded and loaded joints of one rabbit. The superficial zone was designated from the joint surface (at 0 μm) to 8 μm from the joint surface. The mid zone was from 8 to 53 μm, and the deep zone was from 53 to 100 μm. Each image is 100 μm deep and 200 μm wide. Integrated proteoglycan peak absorbance values are pseudo-colored; red indicates that more proteoglycan is present and blue indicates that less proteoglycan is present. These maps were typical of all rabbits.

However, in the deep zone, the amount of proteoglycan increased significantly with loading (p = 0.003). The mean (± SD) of integrated proteoglycan peak values of the control joints (normalized to collagen content) was 0.11 (± 0.07) and 0.17 (± 0.07) for the loaded joints. In all six rabbits, deep zone proteoglycan increased with loading. The mean of percentage increase in deep zone proteoglycan between control and loaded joints was 76%; the median was 46% (Table 5).

Table 5 Zonal distribution of proteoglycan


This is the first study to measure an increase in proteoglycan content due to physiologic in vivo cyclical joint loading. Using microscopic FTIR spectroscopy, we demonstrate that the increase of proteoglycan is localized to the deep zone of cartilage, indicating that 80 cumulative hours of physiological joint loading leads to stimulation of proteoglycan synthesis in a spatially specific manner.

A number of in vitro studies have measured the metabolic effects of cartilage loading using unconfined compression [1014, 19]. Sah et al. [10], Larsson et al. [11], and Parkkinen et al. [19] have observed increased proteoglycan biosynthesis in bovine articular cartilage explants with dynamic compression. In contrast, others have found a decrease in proteoglycan biosynthesis with unconfined compression in vitro [1214]. These difference can be attributed to both the stimulatory effects (fluid pressure, convective transport) [20, 21] and inhibitory effects (matrix consolidation due to large strains) that occur in unconfined compression [14]. Although compressive loading of cartilage explants provides valuable insights, it does not model true load-carrying in physiologic joint function. From in vitro experiments, it has been proposed that stimulation of proteoglycan synthesis is associated with tissue regions having high interstitial fluid flow [22]. However, the fluid flow and lateral expansion of the cartilage in vivo are limited by the surrounding cartilage and bone [23], and it is the pressurization of the interstitial fluid due to these boundaries that exerts the effective load on cartilage [24, 25]. Ikenoue et al.[26] have demonstrated increased aggrecan expression and synthesis in high-density cultures of human chondrocytes that received intermittent hydrostatic pressure of 1, 5, or 10 MPa at 1 Hz. They also demonstrate increased expression of type II collagen; however, collagen protein increased only at high pressure, 10 MPa, and weakly at 5 MPa. The findings of the low-pressure experiments by Ikenoue et al.[26] are most relevant to the present study because we estimate that the hydrostatic pressure generated within the deep zone of the MCP joints in our experiments is approximately 1 to 2 MPa. Our findings support the hypothesis that increased levels of fluid pressure stimulate proteoglycan biosynthesis.

In our study, the increase in proteoglycans was localized to the deep zone of cartilage. This is in agreement with a previous finding in vitro [27] in which proteoglycan synthesis increased by 102% to 114% in the deep zone after 4 hours of dynamic unconfined loading. The same study, however, found that the stimulatory effect was decreased after 8 hours. This loss of effect may be due to the loss of hydrostatic pressure over time. With unconfined compression in vitro, the fluid can flow out from the explant edges, and this may lead to lower hydrostatic pressure and thus lower proteoglycan production than exists in vivo under the same frequencies and amplitudes of loading.

Our results support the proposed hypothesis that high hydrostatic pressure as produced in cyclical joint loading promotes matrix synthesis in cartilage [28]. Aggrecan gene expression may be upregulated by the hydrostatic pressure of physiologic range that is exerted by cyclical in vivo loading in the deep zone of cartilage. The deep zone of cartilage is loaded primarily under hydrostatic pressure and experiences little fluid flow in vivo [29]. Studies by Hall et al. [30] and Parkkinen et al. [19] demonstrate in vitro that hydrostatic pressure increases proteoglycan synthesis in cartilage explants. Chondrocytes are the sole regulators of cartilage biosynthetic activity and respond to external mechanical stimuli such as hydrostatic pressure and fluid shear [10, 28, 31]. Stretch-activated ion channels might be part of the transduction pathway of repetitive forces [32, 33]. We hypothesize that the increase in proteoglycan in the cartilage deep zone is due to the localized increase in hydrostatic pressure caused by cyclical in vivo loading that leads to signal transduction within the resident chondrocytes.

Our experiment is long-term (>3 months), and therefore we expect all components of proteoglycan synthesis to have been upregulated. For example, the genes required for aggrecan synthesis and post-translational modification include the protein core [34], xylosyl tranferase [35], and sulfotransferases [36]. Recently, the transcription rates of genes for sulfotransferases C4ST1, C4ST2, and C6ST1 all have been shown to increase with in vitro dynamic compression [37].

With FTIR microscpectroscopy, no significant change in the amount of collagen is found with 80 hours of cumulative loading. However, this is expected given the extremely long half-life (200 to 400 years) reported for cartilage collagen [38]. The turnover rate of collagen is much slower than that of aggrecan [39, 40]. It should be noted, however, that alterations to the collagen network organization may have occurred without changes in the amount of collagen after loading. Arokoski et al. [41] observed that, although joint loading through long-distance running in dogs generally did not significantly change the thickness of cartilage zones, birefringence intensity decreased in the superficial zone; the authors attributed this decrease to a localized loss of collagen network organization. Because we were unable to measure birefringence intensity, we cannot make detailed conclusions on collagen network organization in this study.

Our study does not determine the minimum number of hours of loading required to detect an increase in proteoglycan, nor whether this increase is sustained, because all joints were loaded for 80 cumulative hours and a study with multiple time points would be required. Also, because a single loading pattern was used, we cannot draw conclusions about the effect of in vivo loading on proteoglycan at other forces and frequencies. Future studies will test other durations, peak forces, and frequencies of in vivo joint loading.


We conclude that cyclical in vivo joint loading increases the proteoglycan content of the cartilage deep zone via signal transduction stimulated by increased hydrostatic pressure (Figure 3). This is clinically significant because the biomechanical properties of cartilage, and therefore its function, depend to a large extent on its ability to maintain hydration and tissue thickness under mechanical stresses with normal physiological loading. Proteoglycans provide the osmotic resistance necessary for cartilage to resist compressive loads.

Figure 3
figure 3

A proposed mechanism by which cyclical loading leads to changes in articular cartilage mechanical properties. Hydrostatic pressure of cartilage tissue is increased through compression caused by cyclical in vivo joint loading. With loading at physiological frequencies and amplitudes, changes in cellular signaling pathways lead to a detectable increase in proteoglycan synthesis. Changes in chemical composition of cartilage extracellular matrix eventually lead to changes in mechanical properties of the tissue in general.

An increase in the amount of cartilage proteoglycan could indicate a healthy mode of joint response to loading in which chondrocytes detect and respond to changes in their mechanical environment by increasing proteoglycan biosynthesis. However, the mechanical effect of changing the ratio of proteoglycan to collagen was not tested and the contents of other matrix proteins were not measured. Nonetheless, using our in vivo joint loading model, we will be able to test different loading patterns to determine thresholds of healthy and damaging loading. These thresholds would be useful in designing force and frequency patterns to prevent overuse joint injuries. Knowledge of the effects of loading patterns may also benefit tissue engineering strategies and post-surgical rehabilitation.



= flexor digitorum profundus


= Fourier Transform Infrared


= glycosaminoglycan


= metacarpophalangeal


= polarized light microscopy


= region of interest


= standard deviation.


  1. Carney SL, Muir H: The structure and function of cartilage proteoglycans. Physiol Rev. 1988, 68: 858-910.

    CAS  PubMed  Google Scholar 

  2. Eyre D: Collagen of articular cartilage. Arthritis Res. 2002, 4: 30-35. 10.1186/ar380.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  3. Urban JP, Maroudas A, Bayliss MT, Dillon J: Swelling pressures of proteoglycans at the concentrations found in cartilaginous tissues. Biorheology. 1979, 16: 447-464.

    CAS  PubMed  Google Scholar 

  4. Maroudas A, Muir H, Wingham J: The correlation of fixed negative charge with glycosaminoglycan content of human articular cartilage. Biochim Biophys Acta. 1969, 177: 492-500.

    Article  CAS  PubMed  Google Scholar 

  5. Kempson GE, Muir H, Swanson SA, Freeman MA: Correlations between stiffness and the chemical constituents of cartilage on the human femoral head. Biochim Biophys Acta. 1970, 215: 70-77.

    Article  CAS  PubMed  Google Scholar 

  6. Maroudas A, Venn M: Chemical composition and swelling of normal and osteoarthrotic femoral head cartilage. II. Swelling. Ann Rheum Dis. 1977, 36: 399-406.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  7. Basser PJ, Schneiderman R, Bank RA, Wachtel E, Maroudas A: Mechanical properties of the collagen network in human articular cartilage as measured by osmotic stress technique. Arch Biochem Biophys. 1998, 351: 207-219. 10.1006/abbi.1997.0507.

    Article  CAS  PubMed  Google Scholar 

  8. Aspden RM, Hukins DW: Collagen organization in articular cartilage, determined by X-ray diffraction, and its relationship to tissue function. Proc R Soc Lond B Biol Sci. 1981, 212: 299-304.

    Article  CAS  PubMed  Google Scholar 

  9. Benninghoff A: Form und Bau der Gelenkknorpel in ihren Beziehungen zur Funktion. Erste Mitteilung: Die modellierenden und formerhaltenden Faktoren des Knorpelreliefs. (Form and shape of the joint cartilages in their relations with the function. First report: the modeling and shape-holding factors of the cartilage relief). Z Gesamte Anatomie Abt. 1925, 1: 43-64.

    Google Scholar 

  10. Sah RL, Kim YJ, Doong JY, Grodzinsky AJ, Plaas AH, Sandy JD: Biosynthetic response of cartilage explants to dynamic compression. J Orthop Res. 1989, 7: 619-636. 10.1002/jor.1100070502.

    Article  CAS  PubMed  Google Scholar 

  11. Larsson T, Aspden RM, Heinegård D: Effects of mechanical load on cartilage matrix biosynthesis in vitro. Matrix. 1991, 11: 388-394.

    Article  CAS  PubMed  Google Scholar 

  12. Torzilli PA, Grigiene R, Huang C, Friedman SM, Doty SB, Boskey AL, Lust G: Characterization of cartilage metabolic response to static and dynamic stress using a mechanical explant test system. J Biomech. 1997, 30: 1-9. 10.1016/S0021-9290(96)00117-0.

    Article  CAS  PubMed  Google Scholar 

  13. Steinmeyer J, Knue S: The proteoglycan metabolism of mature bovine articular cartilage explants superimposed to continuously applied cyclic mechanical loading. Biochem Biophys Res Commun. 1997, 240: 216-221. 10.1006/bbrc.1997.7641.

    Article  CAS  PubMed  Google Scholar 

  14. Wong M, Siegrist M, Cao X: Cyclic compression of articular cartilage explants is associated with progressive consolidation and altered expression pattern of extracellular matrix proteins. Matrix Biol. 1999, 18: 391-399. 10.1016/S0945-053X(99)00029-3.

    Article  CAS  PubMed  Google Scholar 

  15. King KB, Opel CF, Rempel DM: Cyclical articular joint loading leads to cartilage thinning and osteopontin production in a novel in vivo rabbit model of repetitive finger flexion. Osteoarthritis Cartilage. 2005, 13: 971-978. 10.1016/j.joca.2005.06.015.

    Article  CAS  PubMed  Google Scholar 

  16. Wetzel DL, LeVine SM: Imaging molecular chemistry with infrared microscopy. Science. 1999, 285: 1224-1225. 10.1126/science.285.5431.1224.

    Article  CAS  PubMed  Google Scholar 

  17. Lewis EN, Treado PJ, Reeder RC, Story GM, Dowrey AE, Marcott C, Levin IW: Fourier transform spectroscopic imaging using an infrared focal-plane array detector. Anal Chem. 1995, 67: 3377-3381. 10.1021/ac00115a003.

    Article  CAS  PubMed  Google Scholar 

  18. Camacho NP, West P, Torzilli PA, Mendelsohn R: FTIR microscopic imaging of collagen and proteoglycan in bovine cartilage. Biopolymers. 2001, 62: 1-8. 10.1002/1097-0282(2001)62:1<1::AID-BIP10>3.0.CO;2-O.

    Article  CAS  PubMed  Google Scholar 

  19. Parkkinen JJ, Lammi MJ, Helminen HJ, Tammi M: Local stimulation of proteoglycan synthesis in articular cartilage explants by dynamic compression in vitro. J Orthop Res. 1992, 10: 610-620. 10.1002/jor.1100100503.

    Article  CAS  PubMed  Google Scholar 

  20. Maroudas AI: Balance between swelling pressure and collagen tension in normal and degenerate cartilage. Nature. 1976, 260: 808-809. 10.1038/260808a0.

    Article  CAS  PubMed  Google Scholar 

  21. O'Hara BP, Urban JP, Maroudas A: Influence of cyclic loading on the nutrition of articular cartilage. Ann Rheum Dis. 1990, 49: 536-539.

    Article  PubMed Central  PubMed  Google Scholar 

  22. Buschmann MD, Kim Y-J, Wong M, Frank E, Hunziker EB, Grodzinsky AJ: Stimulation of aggrecan synthesis in cartilage explants by cyclic loading is localized to regions of high interstitial fluid flow. Arch Biochem Biophys. 1999, 366: 1-7. 10.1006/abbi.1999.1197.

    Article  CAS  PubMed  Google Scholar 

  23. Mizrahi J, Maroudas A, Lanir Y, Ziv I, Webber TJ: The "instantaneous" deformation of cartilage: effects of collagen fiber orientation and osmotic stress. Biorheology. 1986, 23: 311-330.

    CAS  PubMed  Google Scholar 

  24. Setton LA, Zhu W, Mow VC: The biphasic poroviscoelastic behavior of articular cartilage: role of the surface zone in governing the compressive behavior. J Biomech. 1993, 26: 581-592. 10.1016/0021-9290(93)90019-B.

    Article  CAS  PubMed  Google Scholar 

  25. Soltz MA, Ateshian GA: Experimental verification and theoretical prediction of cartilage interstitial fluid pressurization at an impermeable contact interface in confined compression. J Biomech. 1998, 31: 927-934. 10.1016/S0021-9290(98)00105-5.

    Article  CAS  PubMed  Google Scholar 

  26. Ikenoue T, Trindade MC, Lee MS, Lin EY, Schurman DJ, Goodman SB, Smith RL: Mechanoregulation of human articular chondrocyte aggrecan and type II collagen expression by intermittent hydrostatic pressure in vitro. J Orthop Res. 2003, 21: 110-116. 10.1016/S0736-0266(02)00091-8.

    Article  CAS  PubMed  Google Scholar 

  27. Kiraly K, Hyttinen MM, Parkkinen JJ, Arokoski JA, Lapvetelainen T, Torronen K, Kiviranta I, Helminen HJ: Articular cartilage collagen birefringence is altered concurrent with changes in proteoglycan synthesis during dynamic in vitro loading. Anat Rec. 1998, 251: 28-36. 10.1002/(SICI)1097-0185(199805)251:1<28::AID-AR6>3.0.CO;2-A.

    Article  CAS  PubMed  Google Scholar 

  28. Wong M, Carter DR: Articular cartilage functional histomorphology and mechanobiology: a research perspective. Bone. 2003, 33: 1-13. 10.1016/S8756-3282(03)00083-8.

    Article  CAS  PubMed  Google Scholar 

  29. Carter DR, Beaupre GS, Wong M, Smith RL, Andriacchi TP, Schurman DJ: The mechanobiology of articular cartilage development and degeneration. Clin Orthop Relat Res. 2004, 427 (suppl): S69-77. 10.1097/01.blo.0000144970.05107.7e.

    Article  PubMed  Google Scholar 

  30. Hall AC, Urban JP, Gehl KA: The effects of hydrostatic pressure on matrix synthesis in articular cartilage. J Orthop Res. 1991, 9: 1-10. 10.1002/jor.1100090102.

    Article  CAS  PubMed  Google Scholar 

  31. Collins-Racie LA, Flannery CR, Zeng W, Corcoran C, Annis-Freeman B, Agostino MJ, Arai M, DiBlasio-Smith E, Dorner AJ, Georgiadis KE, et al: ADAMTS-8 exhibits aggrecanase activity and is expressed in human articular cartilage. Matrix Biol. 2004, 23: 219-230. 10.1016/j.matbio.2004.05.004.

    Article  CAS  PubMed  Google Scholar 

  32. Chiquet M: Regulation of extracellular matrix gene expression by mechanical stress. Matrix Biol. 1999, 18: 417-426. 10.1016/S0945-053X(99)00039-6.

    Article  CAS  PubMed  Google Scholar 

  33. Chiquet M, Fluck M: Early responses to mechanical stress: from signals at the cell surface to altered gene expression. Protein Adaptations and Signal Transduction. Edited by: Storey K, Storey J. 2001, Amsterdam: Elsevier, 97-110.

    Chapter  Google Scholar 

  34. Valhmu WB, Palmer GD, Rivers PA, Ebara S, Cheng JF, Fischer S, Ratcliffe A: Structure of the human aggrecan gene: exon-intron organization and association with the protein domains. Biochem J. 1995, 309 (Pt 2): 535-542.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  35. Gotting C, Kuhn J, Zahn R, Brinkmann T, Kleesiek K: Molecular cloning and expression of human UDP-d-Xylose:proteoglycan core protein beta-d-xylosyltransferase and its first isoform XT-II. J Mol Biol. 2000, 304: 517-528. 10.1006/jmbi.2000.4261.

    Article  CAS  PubMed  Google Scholar 

  36. Kusche-Gullberg M, Kjellen L: Sulfotransferases in glycosaminoglycan biosynthesis. Curr Opin Struct Biol. 2003, 13: 605-611. 10.1016/

    Article  CAS  PubMed  Google Scholar 

  37. Szafranski JD, Grodzinsky AJ: The effects of mechanical deformation, tissue age, and culture duration on the transcription of the chondroitin sulfate biosynthesis associated transcription enzymes in a bovine cartilage explants. Osteoarthritis Cartilage. 2005, 13A: S21-

    Google Scholar 

  38. Maroudas A, Palla G, Gilav E: Racemization of aspartic acid in human articular cartilage. Connect Tissue Res. 1992, 28: 161-169.

    Article  CAS  PubMed  Google Scholar 

  39. Bank RA, Bayliss MT, Lafeber FP, Maroudas A, Tekoppele JM: Ageing and zonal variation in post-translational modification of collagen in normal human articular cartilage. The age-related increase in non-enzymatic glycation affects biomechanical properties of cartilage. Biochem J. 1998, 330 (Pt 1): 345-351.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  40. Maroudas A, Bayliss MT, Uchitel-Kaushansky N, Schneiderman R, Gilav E: Aggrecan turnover in human articular cartilage: use of aspartic acid racemization as a marker of molecular age. Arch Biochem Biophys. 1998, 350: 61-71. 10.1006/abbi.1997.0492.

    Article  CAS  PubMed  Google Scholar 

  41. Arokoski JP, Hyttinen MM, Lapvetelainen T, Takacs P, Kosztaczky B, Modis L, Kovanen V, Helminen H: Decreased birefringence of the superficial zone collagen network in the canine knee (stifle) articular cartilage after long distance running training, detected by quantitative polarised light microscopy. Ann Rheum Dis. 1996, 55: 253-264.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

Download references


The authors thank Yuka Nakamura for animal handling, Alex Portnoy for tissue sectioning, and Andrew Burghardt for assistance with the FTIR techniques. This work was supported by the Centers for Disease Control and Prevention, National Institute of Occupational Safety and Health (grant no. OH007786 to KK); National Institutes of Health, National Institute on Aging (grant no. AG17762 to SM); and the University of California, Berkeley Summer Bioengineering Research Program (to ES).

Author information

Authors and Affiliations


Corresponding author

Correspondence to Karen B King.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

ES carried out the FTIR data acquisition and analysis, performed the statistical analyses, and drafted the manuscript. HL carried out the PLM data acquisition and analysis and helped draft the manuscript. SM provided FTIR equipment and expertise and helped edit the manuscript. DR assisted with the in vivo model and helped edit the manuscript. KK conceived of and supervised the project, supervised all data collection and analysis, and edited the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Authors’ original file for figure 3

Rights and permissions

Reprints and permissions

About this article

Cite this article

Saadat, E., Lan, H., Majumdar, S. et al. Long-term cyclical in vivoloading increases cartilage proteoglycan content in a spatially specific manner: an infrared microspectroscopic imaging and polarized light microscopy study. Arthritis Res Ther 8, R147 (2006).

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • DOI: