Intracellular distribution of Tankyrases as detected by multicolor immunofluorescence techniques

¹Dipartimento di Biologia e Biotecnologie, Università di Pavia; ²Istituto di Genetica Molecolare del CNR, Pavia; ³Laboratorio di Analisi Biochimico-Cliniche, IRCCS San Matteo, Pavia, Italy



Correspondence: Dr. Anna Ivana Scovassi, Istituto di Genetica Molecolare CNR, via Abbiategrasso 207, 27100 Pavia, Italy.
Tel. +39.0382.546334 - Fax +39.0382.422286.
E-mail: scovassi@igm.cnr.it

Key words: apoptosis, confocal microscopy, immunocytochemistry, organelles, PARP, Tanky­rases.

Acknowledgements: the authors are grateful to Dr. Patrizia Vaghi, Centro Grandi Strumenti, University of Pavia, for confocal images. This work was supported by the University of Pavia (Fondo di Ateneo per la Ricerca 2010). SG is supported by the Superpig Program (Funds for Promoting Institutional Agreements, Regione Lombardia, Italy).

Contributions: GS, CS, PV, CA, execution of experiments; MGB, AIS, design of experiments and manuscript writing.

Received for publication: 3 November 2011.
Accepted for publication: 24 November 2011.

©Copyright M.G. Bottone et al., 2012
Licensee PAGEPress, Italy
European Journal of Histochemistry 2012; 56:e4
doi:10.4081/ejh.2012.e4





Introduction

Tankyrases (Tanks) 1 and 2 belong to the poly(ADP-ribosylation) family enzymes1,2 and are soluble proteins that can bind to cytoskeletal, microsome and cytosolic proteins.3,4 A small fraction of Tank 1 is localized at telomeres, where it regulates the accessibility of telomeric DNA to telomerase.5 Tank 1 is required for proper assembly of a bipolar spindle, but not for spindle poles themselves.6 The majority of non-telomeric Tanks reside in the cytosol at multiple loci including centrosomes, Golgi complexes and nuclear pore.7,8 Given their association to membrane bound organelles, Tanks could have additional non-nuclear functions as scaffolding proteins regulating the formation of large protein networks in the cytoplasm.9 Our knowledge on Tank subcellular localization is still fragmentary. Taking into account that the expression of these proteins is upregulated in a variety of cancers,10,11,12,13 the analysis of their level and localization could be instrumental to investigate their possible roles in cancer cells. The aim of the present work was to apply multicolor immunofluorescence protocols to detect the intracellular distribution of Tanks. Moreover, we addressed for the first time their dynamic relocation during apoptosis.

Materials and Methods

Cell culture and treatments

Human HeLa cells (ATCC, Rockville, MD, USA) were grown in 75 cm² flasks in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum, 1% glutamine, 100 U of penicillin and streptomycin (Celbio, Pero, Italy) in 5% CO2 humidified atmosphere. Twenty-four hours before the experiments, cells were seeded on glass coverslips and processed for immunofluorescence microscopy.
In order to induce apoptosis, the cells were incubated with either 100 μM etoposide or 1 μg/mL actinomycin D for 20 h. After the treatments, the samples were fixed with 4% formalin formalin for 30 min at 4°C and post fixed with 70% ethanol for 24 h at -20°C.

Indirect immunofluorescence

Samples were rehydrated for 15 min in PBS and then immunolabeled with the antibodies listed in Table 1. All the incubations were performed at room temperature for 1 h. Cells were then counterstained for DNA with 0.1 μg/mL of Hoechst 33258 (Sigma-Aldrich, Milano, Italy) for 10 min, washed with PBS, and mounted in a drop of Mowiol (Calbiochem-Inalco, Milano, Italy) for confocal microscopy.

Confocal fluorescence microscopy

Confocal laser scanning microscopy was performed with a Leica TCS-SP system mounted on a Leica DMIRBE inverted microscope. For fluorescence excitation, an Ar UV laser at 364 nm was used for Hoechst 33258, Ar visible laser at 488 nm for Alexa 488, and He/Ne laser at 543 for Alexa 594. Spaced (0.5 μm) optical sections were recorded using a 63X oil immersion objective. Images were collected in the 1024×1024-pixel format, stored on a magnetic mass memory, and processed by the Leica confocal software.

Results and Discussion

The intracellular distribution of Tanks and microfilaments has been investigated by multicolor immunofluorescence experiments simultaneously using an antibody recognizing Tanks 1-2, Alexa 488-conjugated phalloidin, and a final staining of nuclear DNA with Hoechst 33258 (blue fluorescence). In control HeLa cells, which displayed the typical pattern of the microfilament network (green fluorescence), Tank labeling (red fluorescence) was mainly confined to the cytoplasm, with few spots within the nucleus (Figure 1a).
To address the destiny of Tanks during apoptosis, HeLa cells were incubated with two known apoptogenic drugs,17 i.e. etoposide (Figure 1b) and actinomycin D (Figure 1c). Hoechst staining confirmed that cells were undergoing apoptosis, with clear signs of nuclear condensation and chromatin fragmentation (Figure 1b,c); moreover, apoptotic cells proved to reorganize their cytoskeleton, with fragmentation of the microfilament bundles and the positivity for phalloidin mainly confined to the peripheral cytoplasmic region (Figure 1b,c; green fluorescence). Tanks 1-2 distribution in early apoptotic cells was essentially restricted to the perinuclear cytoplasmic region (Figure 1b,c; red fluorescence). In the advanced steps of the apoptotic process, HeLa cells showed the typical chromatin fragmentation and membrane blebbing (Figure 1b,c; arrows), characterized by the presence of Tanks within the blebs. This observation indicates that during apoptosis Tanks aggregate in the form of large spots and become components of the protein complexes that are released at the cell surface in the late apoptotic steps.18,19
To better explore the cytoplasmic distribution of Tanks, we performed an accurate analysis of their possible colocalization with some organelles, i.e. Golgi apparatus, mitochondria, endoplasmic reticulum and lysosomes. Figure 2 shows the double immunofluorescence analysis of Tanks (red fluorescence) and the mitochondrial pyruvate dehydrogenase (green fluorescence). As expected, normal HeLa cells (panel a) showed a cytoplasmic staining for mitochondria (green fluorescence) that never overlaps with Tank labeling (red fluorescence). In fact, confocal microscopy fluorescence curves shown in panels a’, a’’ of Figure 2, confirmed that Tanks are not resident mitochondrial proteins. In apoptotic cells (panel b), mitochondria appeared to be condensed, and form large aggregates within the cytoplasm; in this condition too, Tanks never colocalized with mitochondria (Figure 2b’,b’’).
The double immunofluorescence analysis for Tanks and Golgi proteins revealed that both antigens colocalize in control HeLa cells (Figure 3a’,a’’) as well as in early (Figure 3b, arrow) and late (Figure 3b, asterisk) apoptotic cells, where Tanks and Golgi proteins were observed within apoptotic blebs (Figure 3b’,b’’: early apoptosis; Figure 3b’’’,b’’’’: late apoptosis).
Figure 4 shows non-apoptotic (a) and apoptotic (b) HeLa cells probed for Tanks (red fluorescence) and the endoplasmic reticulum (green fluorescence). In both samples, the colocalization of Tanks and the endoplasmic proteins was visible, even within apoptotic blebs (Figure 4a’,a’’; Figure 4b’,b’’). Finally, we found that a pool of Tanks colocates with lysosomal proteins in control cells (Figure 5a,a’,a’’). Remarkably, during apoptosis (Figure 5b) there was a size reduction and aggregation of lysosomes in the cytoplasm, and only a fraction of lysosomes appeared to be labeled for Tanks (Figure 5b’,b’’).
Our results increase the knowledge on the intracellular localization of Tanks. More precisely, we focused on the protein fraction resident within the cytoplasm, which was so far less investigated. We demonstrated for the first time that Tanks 1-2 (or different pools of these proteins) not only associate with Golgi apparatus, as already shown,8 but also with other organelles, i.e. endoplasmic reticulum and lysosomes, which all belong to the vacuolar structure of the cells. In this respect, the evidence that Tanks do not colocate with mitochondria is not surprising.
The observation that Tanks can be detected within apoptotic blebs is also original and novel, and suggests that these proteins do not undergo complete proteolytic cleavage during apoptosis. Thus, Tanks represent additional constituents of apoptotic blebs which are known to contain a plethora of heterogeneous cytoplasmic and nuclear aggregates of proteins and nucleic acids to be extruded from the dying cell,19,20 including another member of the poly(ADP-ribose) polymerase family, PARP-1.21,22
Taking into account that similar results have been obtained in HeLa cells driven to apoptosis with either etoposide or actinomycin D (i.e., with drugs that induce apoptosis through completely different mechanisms), it is tempting to speculate that our observations may reflect a general phenomenon; this point needs however to be confirmed by further analyses performed on other cell lines.

Figure 1. Confocal images of HeLa cells after immunolabeling for Tanks 1-2 (red fluorescence) and microfilaments (green fluorescence): a) control cells; b) cells treated with 100 μM etoposide for 20 h; c) cells treated with 1 μg/mL actinomycin D for 20 h. Arrows in b, c: apoptotic cells. DNA was stained with Hoechst 33258 (blue fluorescence). Scale bar: 20 µm.

Figure 2. Confocal optical sections after immunolabeling for Tanks (red fluorescence) and mitochondria (green fluorescence): a) control HeLa cells; b) cells treated with 100 μM etoposide for 20 h. DNA was counterstained with Hoechst 33258 (blue fluorescence). Lines in a, b represent the region where fusion of green/red fluorescence was measured. Upper (a’,b’) and lower (a’’,b’’) panels refer to green and red fluorescence, respectively. Scale bar: 20 µm.

Figure 3. Confocal optical sections after immunolabeling for Tanks (red fluorescence) and Golgi apparatus (green fluorescence): a) control HeLa cells; b) cells driven to apoptosis by a treatment with 100 μM etoposide for 20 h (arrow: early; asterisk: late apoptotic cells). DNA was counterstained with Hoechst 33258 (blue fluorescence). Lines in a and b represent the region where fusion of green/red fluorescence was measured. Upper (a’,b’,b’’’) and lower (a’’,b’’,b’’’’) panels refer to green and red fluorescence, respectively. Scale bar: 20 µm.

Figure 4. Confocal optical sections after immunolabeling for Tanks (red fluorescence) and endoplasmic reticulum (green fluorescence): a) control HeLa cells b) cells treated with 1 μg/mL actinomycin D for 20 h. DNA was counterstained with Hoechst 33258 (blue fluorescence). Lines in a and b represent the region where fusion of green/red fluorescence was measured. Upper (a’,b’) and lower (a’’,b’’) panels refer to green and red fluorescence, respectively. Scale bar: 20 µm.

Table 1. Primary and secondary antibodies used for multicolor immunofluorescence experiments.

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