ABSTRACT
The extracellular matrix (ECM) provides cells with positional information and a mechanical
scaffold for adhesion and migration. It consists of collagens, glycoproteins, proteoglycans,
glycosaminoglycans and molecules that are bound specifically by the ECM, such as certain
growth factors/cytokines, matrix metalloproteinases (MMPs) and processing enzymes
such as tissue transglutaminase and procollagen propeptidases. This finely tuned ecosystem
is dysbalanced in chronic fibrogenesis, which can be regarded as a continuous wound-healing
process and which results in scar formation. Importantly, the ECM directs cellular
differentiation, migration, proliferation, and fibrogenic activation or deactivation.
Partially via defined oligopeptide sequences or structural domains, the ECM transfers
specific signals to cells that act in concert with growth factors/cytokines. These
signals either confer stress activation, with a resultant fibrogenic response, or
stress relaxation, with a fibrolytic response. Alternatively, ECM-derived peptides
can modulate angiogenesis, or growth factor and MMP availability and activity. Current
ECM-related antifibrotic strategies are based on the identification and in vivo application
of ECM-derived biomodulatory peptides, peptide sequences, or their nonpeptidic mimetics.
The latter open the opportunity of oral application and an extended biological half-life.
Examples are peptides derived from collagens VI (stress activation) and XIV (stress
relaxation), or collagenous consensus peptides that remove ECM-bound MMPs and growth
factors. Furthermore, certain peptides can be used as targeting structures to the
fibrogenic lesion.
KEYWORD
angiogenesis - antifibrotic - basement membrane - cirrhosis - collagen - cytokine
- endothelin - endostatin - extracellular matrix - fibronectin - fibrosis - growth
factor - integrin - liver - matrix metalloproteinase (MMP) - myofibroblast - proteoglycan
- signal transduction - stellate cell - tissue inhibitors of metalloproteinase (TIMP)