The genetic information contained in a cell needs the appropriate
environment to express itself, not only the intracellular environment
but also the extracel- lular one. The latter is provided to a great
extent by the molecules which constitute the extracellular matrix. On
the one hand, the matrix creates inter alia the right pH and osmotic
envi- ronment and allows the diffusion of messengers targeting the cell
membrane; on the other hand, it has a mechanical effect whose relevance
began to be understood 28 years ago. Basically, the messages that reach
the cell and are then transported to the genome depend on molecular
conformational flexibility. Molecular structures usually prevail because
they represent states of minimum potential energy cre- ating energy
barriers which are activated through conformational changes. From the
periphery to the nucleus the information flows through the activa- tion
of energy barriers. The tools used to switch from low-energy to high-
energy molecular configurations are: the binding of ligands to their
receptors, gradients of electrochemical potential created by ion pumps,
Ca2+ mobiliza- tion, and phosphorylation and dephosphorylation.
Variation in molecular con- figuration through molecular binding is in
itself sufficient to trigger ion pumps and activate kinases and
phosphatases. This is one aspect of the mechanical role of the
extracellular matrix dealt with herein: the induction of molecular and
supramolecular conformational modifications through interactions with
the cell membrane, which promote the transduction and centripetal
progression of signals.