Bp. Eyden, BRIEF REVIEW OF THE FIBRONEXUS AND ITS SIGNIFICANCE FOR MYOFIBROBLASTIC DIFFERENTIATION AND TUMOR-DIAGNOSIS, Ultrastructural pathology, 17(6), 1993, pp. 611-622
This brief review details the structure, nature, and distribution of t
he fibronexus, and discusses its significance for myofibroblastic diff
erentiation and tumor diagnosis. The fibronexus is a cell surface spec
ialization consisting of intracellular actin filaments and extracellul
ar fibronectin filaments associated with subplasmalemmal plaque materi
al. The fibronexus represents an intercellular junction between myofib
roblasts, but in particular is a device for providing contact between
myofibroblasts and matrix that mediates continuity between intracellul
ar contractile filaments and extracellular matrix proteins. Immunoelec
tron microscopy in particular has shown that the intracellular filamen
ts contain actin. The extracellular filaments contain fibronectin and
collectively form the fibronectin fibril. The plaque probably contains
such proteins as vinculin, talin, alpha-actinin, and integrin. Under
appropriate biologic development and fixation conditions, the fibronec
tin fibril of the fibronexus is characterized by and distinguished fro
m lamina by enhanced density, a rigid appearance, failure to adhere cl
osely to the contours of the cell surface (except focally near the pla
que material), and a longitudinally filamentous substructure. Confirma
tion of the presence of a fibronectin fibril may be obtained by the fi
nding of intense cell surface staining with an antifibronectin antibod
y. Problems in identifying the fibronexus may be encountered, however,
due to poor development and fixation, in which case the filamentous s
ubstructure may be inapparent. The fibronexus is such a typical featur
e of and is often so conspicuous in myofibroblasts that it can be rega
rded as, perhaps essential for the interpretation of myofibroblastic d
ifferentiation. Structures with a similar appearance have been documen
ted in fundamentally nonmyofibroblastic cells; these include aortic an
d scleral spur smooth muscle cells and endothelium. Uncertainties rema
in in the protein composition of the fibronexus, the nature of its con
tact with the matrix, and its relationship to similar structures seen
in nonmyofibroblastic cells. Immunoelectron microscopy provides a pote
ntial means of clarifying some of these questions.