Association of enhanced expression of gap junctions with in vitro chondrogenic differentiation of rat nasal septal cartilage-released cells followingtheir dedifferentiation and redifferentiation
S. Loty et al., Association of enhanced expression of gap junctions with in vitro chondrogenic differentiation of rat nasal septal cartilage-released cells followingtheir dedifferentiation and redifferentiation, ARCH ORAL B, 45(10), 2000, pp. 843-856
The nasal septum is an important centre of endochondral ossification during
the development of the facial region. Previous studies have shown that it
is possible to recapitulate the differentiation programme of 21-day-old rat
nasal chondrocytes in vitro. The purpose now was to investigate, in vitro,
the cell condensation phase that represents the earliest morphological eve
nt associated with cartilage differentiation in skeletal development. The s
tudy focuses on the ability of the cells to form condensations before overt
differentiation, with special emphasis on gap-junction expression. The gap
-junction protein connexin 43 was localized by indirect immunofluorescence
as primarily intracellular and, on day 5, at the condensation stage, as spo
t-like contacts between cells. Intracellular injection of the permeable dye
Lucifer yellow led to the staining of up to 20 neighbouring cells, indicat
ing functional gap junctions and coupling, In contrast, treatment of cultur
es with the gap-junction blocker glycyrrhetinic acid inhibited dye coupling
and reduced cartilage differentiation. Northern blotting of connexin 43 mR
NA showed a faint band during the first days of culture, with a striking in
crease after day 4. In addition, the mRNA of the homeodomain-containing gen
e Cart-1 began to be expressed in prechondrogenic condensations and corresp
onded to the expression of type II collagen mRNA. These data indicate that
the early stage of in vitro chondrocyte differentiation is the formation of
cell condensations and the ability to establish cell-to-cell communication
. Connexin 43, together with other molecular mechanisms. mediates the conde
nsation phase of chondrogenesis and sets up the optimal environment in whic
h nasal septal cells may terminally differentiate into chondrocytes. (C) 20
00 Elsevier Science Ltd, All rights reserved.