PKCι depletion initiates mitotic slippage-induced senescence in glioblastoma
Ian J Restall1,2, Doris A E Parolin1, Manijeh Daneshmand1
1a Centre for Cancer Therapeutics; Ottawa Hospital Research Institute ; Ottawa , ON Canada.
Abstract:
Cellular senescence is a tumor suppressor mechanism where cells enter a permanent growth arrest following cellular stress. Oncogene-induced senescence (OIS) is induced in non-malignant cells following the expression of an oncogene or inactivation of a tumor suppressor. Previously, we have shown that protein kinase C iota (PKCι) depletion induces cellular senescence in glioblastoma cells in the absence of a detectable DNA damage response. Here we demonstrate that senescent glioblastoma cells exhibit an aberrant centrosome morphology. This was observed in basal levels of senescence, in p21-induced senescence, and in PKCι depletion-induced senescence. In addition, senescent glioblastoma cells are polyploid, Ki-67 negative and arrest at the G1/S checkpoint, as determined by expression of cell cycle regulatory proteins. These markers are all consistent with cells that have undergone mitotic slippage. Failure of the spindle assembly checkpoint to function properly can lead to mitotic slippage, resulting in the premature exit of mitotic cells into the G1 phase of the cell cycle. Although in G1, these cells have the replicated DNA and centrosomal phenotype of a cell that has entered mitosis and failed to divide. Overall, we demonstrate that PKCι depletion initiates mitotic slippage-induced senescence in glioblastoma cells. To our knowledge, this is the first evidence of markers of mitotic slippage directly in senescent cells by co-staining for senescence-associated β-galactosidase and immunofluorescence markers in the same cell population. We suggest that markers of mitotic slippage be assessed in future studies of senescence to determine the extent of mitotic slippage in the induction of cellular senescence.
Insights
Protein kinase C iota (PKCι) depletion causes glioblastoma cells to enter senescence via mitotic slippage, not DNA damage. Senescent cells show abnormal centrosomes and polyploidy, indicating failed cell division.
Area of Science:
- Oncology
- Cell Biology
- Molecular Biology
Background:
- Cellular senescence is a key tumor suppressor mechanism involving permanent cell growth arrest.
- Oncogene-induced senescence (OIS) is a specific type of senescence triggered by oncogene activation or tumor suppressor inactivation.
- Previous work indicated protein kinase C iota (PKCι) depletion induces senescence in glioblastoma cells without DNA damage.
Purpose of the Study:
- To investigate the mechanism of PKCι depletion-induced senescence in glioblastoma cells.
- To characterize the morphological and cell cycle features of senescent glioblastoma cells.
- To determine if mitotic slippage contributes to senescence in these cells.
Main Methods:
- Induction of senescence in glioblastoma cells via PKCι depletion, p21 expression, or basal conditions.
- Analysis of centrosome morphology using immunofluorescence.
- Assessment of cell cycle status, ploidy, and proliferation markers (Ki-67).
- Co-staining for senescence-associated β-galactosidase and immunofluorescence markers.
Main Results:
- Senescent glioblastoma cells exhibited aberrant centrosome morphology across different senescence induction methods.
- These cells were polyploid, Ki-67 negative, and arrested at the G1/S checkpoint, consistent with mitotic slippage.
- The study provides the first direct evidence of mitotic slippage markers within senescent cells.
Conclusions:
- PKCι depletion induces senescence in glioblastoma cells through a mechanism involving mitotic slippage.
- Aberrant centrosome morphology and polyploidy are key features of this senescence type.
- Future senescence studies should assess mitotic slippage markers to understand their role in senescence induction.
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