Pi. Francz et al., DIFFERENTIATION AND POLYPEPTIDE EXPRESSION IN HUMAN PAPILLA AND DERMAL FIBROBLASTS INVITRO, European journal of cell biology, 60(2), 1993, pp. 337-345
Proliferation and differentiation of human scalp hair follicle PaPilla
fibroblasts (PF) in the anagenic stage of development and of neighbor
ing dermal fibroblasts (DF) of the same donor were studied with stem c
ell system-specific methods in primary and secondary populations in in
vitro systems. Both populations differentiate along the sequence of m
itotic fibroblasts (MF) MF I-MF II-MF III and postmitotic fibroblasts
(PMF) PMF IV-PMF V-PMF VI-PMF VIIa/PMF VIIb, as described for fibrobla
st stem cell systems in general elsewhere (Bayreuther et al., Mutat. R
es. 256, 233-242 (1991)). PF and DF populations are distinguished by a
number of cell-biological parameters, like population dynamics, maxim
al cumulative population doublings (CPD), changes in cell type frequen
cies, changes in cloning efficiency as a function of the CPD level (CP
DL) of mitotic mass population, in addition by distinct changes of cel
l type frequencies of postmitotic fibroblasts as a function of the dur
ation of maintenance of postmitotic fibroblast population in stationar
y culture. Primary and secondary PFs express cell type-specific high m
olecular weight cellular polypeptides in the M(r) range of 190 to 270
x 10(3) and/or secrete cell type-specific low molecular weight polypep
tides in the M(r) range of 27 to 28 x 10(3) as revealed by two-dimensi
onal gel electrophoresis of [S-35]methionine-labeled and [C-14]proline
-labeled polypeptides. These polypeptides are not expressed in the cor
responding primary or secondary DF cell types. The expression of speci
fic proteins in primary and secondary PF in vitro may correspond to sp
ecific functions of PF in vivo.