The question about microtubule length in interphase cells has become actual
now, because parametres of dynamic instability of the plus end of microtub
ules measured in vivo cannot account for a rapid turnover of long microtubu
les. This problem may be solved assuming that microtubules rapidly turnover
via depolymerization from the minus end and/or the real length of microtub
ules is much shorter than the considered one.
We traced microtubules radiating from the centrosome in epitelial cells (PK
and FBT) and in fibroblasts (MEF and L) in the area of 4,0 x 5,5 x 1,5 mu
m with centrioles in its center and microtubules in a large portion of the
cytoplasm in PK cells. The number of microtubules analysed around the centr
osome was no less than 200 for each cell line.
In all cell lines studied, microtubules radiating from the centrosome were
typically no longer than 1 mu m, and about 1/3 of microtubules were 0,2-0,4
mu m long. Only 2,5-8% of microtubules radiating from the centrosome run o
ut of the area studied. The mean length of microtubules surrounding the cen
trosome in all cell lines examined was 0,4-0,8 mu m. The average length of
microtubules attached to the centrosome was less than that of free microtub
ules. Thus, almost all microtubules around the centrosome are short, and on
ly a few attached microtubules can reach the cell periphery. The reconstruc
tion of cytoplasmic microtubules in PK cell was undertaken in an area of 10
x 35 mu m. In the lamella, the mean length of microtubules is about 1,6 mu
m and the majority of microtubules are 0,5 to 1,5 mu m long. The results o
btained support the hypothesis [1] that the majority of microtubules in int
erphase cell are not associated with the centrosome.