Bp. Eyden et al., DEFINING THE MYOFIBROBLAST - NORMAL-TISSUES, WITH SPECIAL REFERENCE TO THE STROMAL CELLS OF WHARTONS JELLY IN HUMAN UMBILICAL-CORD, Journal of submicroscopic cytology and pathology, 26(3), 1994, pp. 347-355
Cells differing widely in tissue distribution, immunophenotype and ult
rastructure have been described as myofibroblasts. The definition of t
he myofibroblast was analysed as applied to normal tissues, with origi
nal observations on Wharton's jelly stromal cells as an example. Strom
al cells in Wharton's jelly were studied by conventional histology, im
munohistochemistry, and electron microscopy. The normal architecture o
f the cord was confirmed by light microscopy. Stromal cells and the sm
ooth-muscle cells of the umbilical vessels were positive for vimentin,
desmin and alpha-smooth muscle actin, while only the stromal cells we
re positive for prolyl 4-hydroxylase. Electron microscopy revealed var
iable but sometimes only moderate amounts of rough endoplasmic reticul
um, bundles of smooth-muscle type filaments with focal densities, a la
rge Golgi apparatus with collagen secretion granules, lipid and glycog
en. There was no convincing evidence for either lamina or fibronexus j
unctions. The nature of the stromal cell was discussed in the light of
these findings. It was concluded that a myofibroblastic designation w
as inappropriate and that these cells had phenotypic similarities to v
ascular smooth muscle cells. The possibility is proposed that most exa
mples of spindle cells cited in the literature as being myofibroblasts
and seen in normal tissues not subjected to trauma or showing patholo
gy may be pericytic or smooth-muscle in nature.