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Dr Alvin Kwan

Dr Alvin Kwan


School of Biosciences

+44 (0)29 2087 4654
Sir Martin Evans Building, Museum Avenue, Cardiff, CF10 3AX

Through my role as the Head of International, I am responsible for implementing the School’s internationalization programme which includes international student recruitment, student/staff exchange and the development of teaching and research links with partner universities overseas.

Research overview:

  1. Cell and extracellular matrix biology of cartilage development
  2. Metalloproteinases in atherosclerosis
  3. The role of haemodialysates in phenotypic modulation of macrophages in tissue repair


  • Head of International
  • Deputy Head of Student Mobility
  • Assessment Lead: BI2333 Practical Anatomy







The regulation of chondrocyte maturation during endochondral ossification

Bones grow and repair mainly via a complex developmental process known as endochondral ossification in which ossification occurs within a specialised hyaline cartilaginous matrix. In the long bones, this hyaline cartilage is known as the epiphyseal growth plate. Within the growth plate, chondrocytes undergo a stringently controlled developmental sequence leading to terminal chondrocyte differentiation (cell hypertrophy) prior to the transition from cartilage to bone. Chondrocyte differentiation is therefore an important prerequisite of normal bone formation. Current research activities in my laboratory have focussed mainly on two potential regulators of cell differentiation in the growth plate.

  1. Type X collagen – an extracellular matrix molecule which forms a mat-like network around differentiating chondrocytes in the hypertrophic cartilage matrix. Its expression is reinitiated in mature articular cartilage in osteoarthritis and is thought to be the consequence of tissue repair and osteophyte formation. We have identified several receptors for type X collagen on the surface of hypertrophic chondrocytes, these include the integrin a 2 b 1 and the collagen receptors DDR1 and DDR2. We are particularly interested in studying the mechanisms of interactions, the biological effects and signalling events following receptor-type X binding.
  2. Small Acidic Protein (SAP) – a 172 amino acid bHLH-like nuclear protein which is downregulated during chondrocyte hypertrophy and by cyclopamine, an inhibitor of the Hedgehog signalling pathway. We hypothesise that SAP is a novel transcription factor that attenuates chondrocyte differentiation in the epiphyseal growth plate. We are interested in investigating the roles of SAP in endochondral ossification and the characterization of the Hedgehog-responsive element(s) of the SAP gene. We also study the regulation of SAP expression in other disease models such as atherosclerosis.


  • Drs. Farquharson & D. Jefferies, Roslin Institute ( Edinburgh), Midlothian, Scotland
  • Professor Vic Duance, Cardiff School of Biosciences, Cardiff University
  • Dr Birgit Leitinger, Division of Biomedical Sciences, Imperial College,London
  • Dr Sam Evans, Cardiff School of Engineering, Cardiff University
  • Dr Dipak Ramji, Cardiff School of Biosciences, Cardiff University
  • Dr Yoshiharu Mizui, Eisai Co. Ltd., Tsukuba Research Laboratories, Japan