Both mitotic and apoptotic cells display hypercondensation of the chromatin
and loss of the nuclear envelope (Lazebnik et at., 1993). Herein, we descr
ibe a third similarity between the two processes. We have observed, initial
ly in apoptotic cells of the PC-12 lineage clusters of 40-60 (similar to 50
) nm vesicles adjoined by a minor contingent of tubule vesicular elements o
f 100-200 nm which are indistinguishable from their vesicular counterparts
in mitotic PC-12 cells. The clusters of similar to 50 nm vesicles were subs
equently observed in all studied rat tissue cells in apoptosis (plasma cell
s and macrophages, secretory epithelial cells from pancreatic acini, ventra
l lobe of prostate and mammary gland). Clusters of similar to 50 nm vesicle
s comparable to those of the PC-12 cells were found in HeLa cells treated w
ith human alfa TNF, in WEHI-3 cells exposed to VM 26 (a teneposide) (Sesso
et at., 1997) and in HL-60 cells treated with thapsigargin, PC-12 and HeLa
cells affixed to coverslips were double labelled and examined with the fluo
rescence microscope to reveal simultaneously the disposition of the chromat
in with Hoechst stain and the distribution of the fluorescence of Golgi or
of Golgi-associated proteins. A common pattern of fluorescence was observed
in a minor proportion of apoptotic cells using three different antibodies
used. The label frequently appeared as finely dispersed granules in the cyt
oplasm. In some apoptotic cells, relatively coarse granules were observed.
This pattern of label distribution is compatible with the disposition of ve
sicular clusters we have encountered in apoptotic PC-12 cells sectioned ser
ially or semi serially. In such sections of both mitotic and apoptotic PC-1
2 cells, we noticed that the conglomerates of 50 nm vesicles were frequentl
y associated with cisternae of the rough ER. Vesicles of similar size were
also noted pinching off from the extremities of Golgi cisternae reduced in
size, These cisternae diminish in length and width when they are in the pro
cess of disassembling at the very beginning of mitosis and in apoptosis.