Literature DB >> 2758065

The influence of link protein stabilization on the viscometric properties of proteoglycan aggregate solutions.

V C Mow1, W Zhu, W M Lai, T E Hardingham, C Hughes, H Muir.   

Abstract

The dynamic, steady-shear and transient shear flow properties of precisely prepared link-stable (s0 136, 66% aggregate) and link-free (s0 93, 59% aggregate) proteoglycan aggregate solutions at concentrations ranging from 10 to 50 mg/ml were determined using a cone-on-plate viscometer in a mechanical spectrometer. All proteoglycan solutions tested possessed: (1) linear viscoelastic properties - as measured by the dynamic complex modulus under small amplitude steady oscillatory conditions (1 less than or equal to omega less than or equal to 100 rad/s) - and (2) nonlinear shear-rate dependent apparent viscosities and primary normal stress difference under steady shearing conditions (0.25 less than or equal to gamma less than or equal to 250 s-1). Our transient flow data show that all proteoglycan aggregate solutions exhibited transient stress overshoot effects in shear stress and normal stress. From these steady and transient flow data, we conclude that link protein stabilized aggregates have significant effects on their dynamic and steady-shear properties as well as transient flow properties. The transient stress overshoot data provide a measure of the energy per unit volume of fluid required to overcome the proteoglycan networks in solution from a resting state. Thus we found that link-stable aggregates form much stronger networks than link-free aggregates. This is corroborated by the fact that link-stable aggregates form more elastic (lower than delta) and stiffer (higher [G*]) networks than link-free aggregates. The complete spectrum of viscometric flow data is entirely compatible with the proposed role of link protein in adding structural stability to the proteoglycan-hyaluronate bond. In cartilage, the enhanced strength of the networks formed by link-stable aggregates may play an important role in determining the material properties of the tissue and thereby contribute to the functional capacity of cartilage in diarthrodial joints.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2758065     DOI: 10.1016/0304-4165(89)90011-1

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  5 in total

1.  Interstitial fluid flow in tendons or ligaments: a porous medium finite element simulation.

Authors:  S L Butler; S S Kohles; R J Thielke; C Chen; R Vanderby
Journal:  Med Biol Eng Comput       Date:  1997-11       Impact factor: 2.602

2.  Fixed electrical charges and mobile ions affect the measurable mechano-electrochemical properties of charged-hydrated biological tissues: the articular cartilage paradigm.

Authors:  Leo Q Wan; Chester Miller; X Edward Guo; Van C Mow
Journal:  Mech Chem Biosyst       Date:  2004-03

3.  Studies of the articular cartilage proteoglycan aggrecan in health and osteoarthritis. Evidence for molecular heterogeneity and extensive molecular changes in disease.

Authors:  G Rizkalla; A Reiner; E Bogoch; A R Poole
Journal:  J Clin Invest       Date:  1992-12       Impact factor: 14.808

4.  Macromolecular diffusion of biological polymers measured by confocal fluorescence recovery after photobleaching.

Authors:  P Gribbon; T E Hardingham
Journal:  Biophys J       Date:  1998-08       Impact factor: 4.033

5.  Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage.

Authors:  Aarti Sharma; Lindsay D Wood; James B Richardson; Sally Roberts; Nicola J Kuiper
Journal:  Arthritis Res Ther       Date:  2007       Impact factor: 5.156

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.