Anoctamin 6 differs from VRAC and VSOAC but is involved in apoptosis and supports volume regulation in the presence of Ca2+
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Anoctamin 6 (ANO6), also known as TMEM16F, has been shown to be a calcium-activated anion channel with delayed calcium activation. The cellular function of ANO6 is under debate, and different groups have come to different conclusions about ANO6’s physiological role. Although it is now quite well established that ANO6 is distinct from the volume-regulated anion channel, it is still unclear whether ANO6 or other anoctamins can be activated by cell swelling. In this study, we suggest that ANO1, ANO6, and ANO10 do not contribute to the volume-activated current in ANO-overexpressing HEK293 cells. Furthermore, knock-down of ANO6 in Ehrlich ascites tumor cells (EATC) and Ehrlich–Lettre ascites (ELA) did not decrease but instead significantly increased swelling-activated membrane currents. Knock-down of ANO6 in EATC did not reduce regulatory volume decrease (RVD) in the absence of extracellular calcium, whereas it significantly reduced RVD in the presence of calcium. Interestingly, we found that knock-down of ANO6 in ELA cells resulted in a decrease in cisplatin-induced caspase-3 activity, confirming earlier findings that ANO6 is involved in apoptosis. Finally, knock-down of ANO1 and ANO6 did not affect the volume-sensitive release of taurine in ELA cells. Thus, our data provide evidence that ANO6 cannot be activated directly by cell swelling unless Ca2+ is present. We also conclude that ANO6 carries a current during RVD, provided extracellular calcium is present. Thus, swelling activation of ANO6 requires the presence of free calcium.
KeywordsANO6 TMEM16F VRAC Volume regulation Apoptosis
Anoctamin 6 (ANO6), also known as TMEM16F, is a member of the anoctamin family of transmembrane proteins, which comprises ten members in vertebrates (ANO1–10). Three of the members, ANO1, ANO2, and ANO6 have convincingly been shown to be calcium-activated chloride channels (CaCCs) [2, 9, 28, 31, 32, 33, 36], whereas the functions of the remaining members are less well known. Several anoctamins are known to be mutated or dysregulated in human diseases, such as musculoskeletal disorders, ataxias, and several types of cancer, which emphasizes the need to thoroughly study them . ANO6 is interesting because it has been shown that mutations in this protein are the cause of the congenital bleeding disorder Scott syndrome in humans . ANO6’s involvement in blood coagulation was confirmed in a study of ANO6 knock-out mice, which showed prolonged bleeding time compared with wild-type (WT) mice . Another knock-out mouse study suggested that ANO6 is also important for embryonic development of skeletal tissues . Finally, changes in alternative splicing of human ANO6 are associated with the development of metastasis in breast cancer . ANO6 has been suggested to be involved in a diverse array of processes in the cell, such as externalization of phosphatidylserine [23, 34], cell volume regulation , and cell migration . Although it is now well established that ANO6 constitutes a Ca2+- and depolarization-activated anion channel [1, 24, 31, 33], Yang et al. found that it was a nonselective cation channel . Our group recently conducted a thorough investigation of the properties of the ANO6 channel . We found that ANO6 is a plasma membrane-located Ca2+-activated anion channel with a relatively high cation permeability that is correlated with the ANO6-associated anion permeability (PNa = 0.3 PCl). ANO6’s properties differed significantly from those of ANO1, including a markedly higher EC50 for Ca2+ and a delay of several minutes from cytosolic (Ca2+) increase to Cl− current activation.
In a study from Almaca et al., it was suggested that some anoctamins, including ANO6, contribute to the swelling-activated chloride current (I Cl, swell) . Knock-down (KD) of ANO6 significantly reduced I Cl, swell and impaired the cell’s ability to undergo regulatory volume decrease (RVD) in response to osmotic cell swelling. Recently, however, the results of Shimizu et al. showed that ANO6 is different from the volume-regulated anion channel (VRAC) . Furthermore, Kunzelmann et al. excluded ANO6 as a VRAC candidate, as ANO6 has none of the characteristic fingerprints of VRAC, i.e., isovolumic activation by a decrease in intracellular ionic strength or cell perfusion with GTPγS . Finally, our studies indicated a significant difference between the two channels as revealed by their current responses to a step voltage protocol. Following the initial ohmic current response to a V-step into the positive region of membrane potentials, ANO6 currents are slowly activated [9, 25] in contrast to VRAC currents which are known to be slowly deactivated [12, 24]. ANO6 is thus not identical with VRAC. However, there are still ongoing discussions as to whether ANO6 is activated by cell swelling and whether ANO6 contributes to RVD. This is investigated in the present study. Additionally, we looked at the relation between ANO6 and another still unidentified anion channel, the volume-sensitive organic osmolyte and anion channel (VSOAC), which has previously been suggested to be identical to VRAC, although convincing evidence now indicate that they are distinct channels . Finally, we examined the possible role of ANO6 in cisplatin-induced apoptosis, which is a process that is highly dependent on cell shrinkage .
Materials and methods
Cell culture and transfection
Three different model cell lines were used: The mouse-derived Ehrlich ascites tumor cells (EATC) and Ehrlich–Lettre ascites (ELA) cells and the human-derived human embryonic kidney 293 (HEK293) cells. All cells were maintained at 37 °C aerated with 5 % CO2:95 % O2. HEK293 cells were maintained in DMEM and EATC and ELA cells were kept in RPMI-1640. 10 % fetal bovine serum and 1 % penicillin/streptomycin were added to each media. The medium for the EATC and ELA KD clones and the EATC overexpression clones was supplemented with 10 μg/mL blasticidin to select for resistant clones. EATC and ELA cells were transfected using Lipofectamine 2000 (Invitrogen, Taastrup, Denmark) and HEK293 cells using Trans-IT®-293 (Mirus Bio LLC, Madison, WI, USA). HEK293 cells were used for electrophysiological recordings 24–48 h after transfection.
Isolation of RNA, reverse transcription, PCR, and cDNA cloning
Total RNA was isolated from EATC using the RNeasy Mini Kit (Qiagen, Ballerup, Denmark). cDNA was prepared in a total volume of 40 μL by hybridization of 500 ng oligo dT primers to 4 μg RNA at 65 °C for 5 min followed by extension at 42 °C for 50 min in the presence of 200 U Superscript II reverse transcriptase (Invitrogen, Brondby, Denmark), 500 μM dNTP, 10 μM DTT, 50 mM Tris–HCl, 75 mM KCl, and 3 mM MgCl2, pH 8.3. Finally, the RT was inactivated at 70 °C for 15 min. PCR was performed in a total volume of 20 μL containing 1 μL of the RT reaction, 0.5 mM dNTPs, 0.5 μM of each primer, 2 mM MgCl2 and 2 U Taq polymerase in PCR buffer (conventional PCR) or 2 U Pfu Ultra II fusion HS polymerase (Stratagene, Santa Clara, CA, USA) in Pfu PCR buffer (for cloning). PCR consisted of a denaturizing step of 2 min at 95 °C followed by 35 cycles of 95 °C in 30 s, 58 °C in 30 s and 72 °C in 2 min. Primers used for PCR were: Ano1_for; 5′-gacctgggctat gaggttca-3′, Ano1_rev; 5′-ggctgatgtctttggggata-3′, Ano6_for; 5′-gcagcccttggatcttatca-3′, Ano6_rev; 5′-tgctgtagctcaacggtg tc-3′, Ano10_for; 5′-tctgagtggaccagccttct-3′, Ano10_rev; 5′-agaagagtgaggcgaagcaa-3′. Primers used to clone and generate attB-flanked gateway compatible PCR products were Ano6_for; 5′-ggggacaagtttgtacaaaaaagcaggcttcaccatgcagatgatgactaggaaggtc-3′, Ano6_rev; 5′-ggggaccactttgtacaagaaagctgggtctcattcgagttttggccgcacg-3′, Ano1_for; 5′-ggggacaagtttgtacaaaaaagcaggcttcaccatgagggtccccgagaagtac-3′, Ano1_rev; 5′-ggggaccactttgtacaagaaagctgggtcctacagcgcgtccccatggga-3′, Ano10_for; 5′-ggggacaagtttgtacaaaaaagcaggcttcaccatgagagtgactttatcaacgctg-3′, Ano10_rev; 5′-ggggaccactttgtacaagaaagctgggtctcaggtagcttccttcccatct-3′. PCR products were excised from 0.8 % agarose gels and DNA extracted using E.Z.N.A gel extraction kit (Omega Bio-tek, Norcross, GA, USA). PCR products of mAno6, mAno1 or mAno10 were then recombined into pDONR221 using BP Clonase according to the manufacturer’s instructions (Invitrogen, Taastrup, Denmark) to generate mAno6, mAno1 or mAno10 entry clones. After transformation into E. coli and selection using 50 μg/mL kanamycin, DNA was purified and inserts in entry clones confirmed by full-length DNA sequencing. Finally, using LR-clonase mix, the inserts from entry clones were recombined into pcDNA6.2/EmGFP-Bsd/V5-DEST and pcDNA3.1-DEST47 to generate vectors co-expressing mANO6, mANO1 or mANO10 and EmGFP. Expression plasmids were produced in E. coli using ampicillin (100 μg/mL) as selection agent.
Gel electrophoresis and Western blotting
Cells were lysed in 95 °C lysis buffer (150 mM NaCl, 20 mM HEPES, 1 mM EDTA, 10 % Glycerol, 0.5 % Triton X-100, and 0.5 % SDS) with protease inhibitors (Roche Applied Science) and phosphatase inhibitors added. The lysates were subsequently homogenized, and the supernatant was collected by centrifugation. Protein concentrations were determined using Bio-Rad DC protein assay. SDS-polyacrylamide gel electrophoresis were performed using a 10 % gel (Invitrogen) and transferred to nitrocellulose membranes. The membranes were dyed with Ponceau Red (Sigma) and washed in TBST (10 mM Tris · HCl, pH 7.5, 120 mM NaCl, and 0.1 % Tween 20) before being blocked in a 5 % nonfat dry milk and TBST solution. Membranes were incubated with primary antibody at following concentrations: 1:50 ANO6 (gift from Prof. Kunzelmann), 1:8000 Alpha-tubulin. Membranes were washed in TBST before introduction to secondary antibody (Sigma) 1:5000. The protein bands were visualized using 5-bromo-4-chloro-3-indolyl phosphate-nitro blue tetrazolium (BCIP/NBT; Kirkegaard and Perry Lab) and scanned or alternatively visualized using using enhanced chemiluminiscence using horseradish peroxidase and luminol.
Construction of microRNA plasmids
Interfering microRNA (miRNAi) KD of mANO6 and mANO1 was achieved using BLOCK-iT™ Pol II miR RNAi Expression technology (Invitrogen, Taastrup, Denmark). miRNAi targeting mAno6 and mAno1 were designed using Invitrogen’s online design tool generating sense and antisense single-stranded DNA strings (ssDNA). DNA sequences were: ANO6, sense, 5′-tgctgtttagcgggagtttgatgtgcgttttggccactgactgacgcacatcactcccgctaaa-3′, antisense, 5′-cctgtttagcgggagtgatgtgcgtcagtcagtggccaaaacgcacatcaaactcccgctaaac-3′; ANO1, sense, 5′-gacctgggctat gaggttca-3′ and antisense 5′-ggctgatgtctttggggata-3′. The two ssDNAs were annealed in annealing buffer generating a dsDNA, which was then ligated into pcDNA™6.2-GW/EmGFP-miR generating miR-ANO6-KD or miR-ANO1-KD plasmids. Plasmids were transformed into omnimax T-1 E. coli (Invitrogen, Taastrup, Denmark) and selected using spectinomycin as antibiotic (50 μg/μL). Plasmid inserts were confirmed by sequencing.
Generation of mANO6 or mANO1 stable KD in EATC and ELA
EATC and ELA cells were transfected with miR-ANO6-KD or miR-ANO1-KD plasmids using Lipofectamine 2000 (Invitrogen, Taastrup, Denmark), incubated for 4 h and then re-suspended in fresh medium containing 10 μg/mL blasticidin. After 1 week selection, single cells were picked and transferred to 24- or 96-well trays and allowed to grow into a full clone in the presence of blasticidin. Clones were analyzed using qPCR (as described above) and, if possible, using Western blot analysis . The selected EATC KD clone was named miR-ANO6-1 (EATC ANO6-KD) and the selected ELA KD clones were named miR-ANO6-10 (ELA ANO6-KD), miR-ANO6-15 and miR-ANO1-7 (ELA ANO1-KD).
Cells were plated on poly-l-lysine-coated cover slips. In experiments with overexpression of ANO proteins, transfected cells were identified by their EmGFP expression using a fluorescence microscope. Whole-cell voltage-clamp recordings were performed with the Axopatch 200B amplifier interfaced to a Digidata 1440A using pClamp10 for recording and analysis (Molecular Devices). Analog signals were acquired at 2.5 kHz and filtered at 1 kHz. All recordings were performed at room temperature (20 °C). Patch pipettes were fabricated from borosilicate glass capillaries using a DMZ-Universal Puller (Zeitz Instruments, Munich, Germany) with a resistance of 2–5 MΩ when filled with the internal solution. For activation of I Cl, swell, the pipette solution contained (in mM): CsCl, 90; MgCl2, 2; EGTA, 10; HEPES, 10; Na2-ATP, 5, pH 7.2 with TRIS or NaOH and osmolality adjusted to 295 mOsmol/kg with D-mannitol. The bath was a modified Ringer’s solution and, in the EATC and HEK293 experiments, it contained (in mM): NaCl, 90; CaCl2, 1; MgCl2, 1; and HEPES, 10, at pH 7.4 with TRIS and osmolality adjusted to 190 mOsmol/kg (hypotonic) or 300 mOsmol/kg (isotonic) with d-mannitol. For ELA experiments, the bath contained (in mM): NaCl, 150; CaCl2, 1.5; MgCl2, 1; HEPES, 10; glucose, 10, pH 7.4 with NaOH and osmolality adjusted to 317 mOsmol/kg (isotonic) with d-mannitol. To produce the hypotonic bath, the isotonic solution was diluted 30 % (final osmolality: 222 mOsmol/kg). Osmolality was measured using a vapor pressure depression osmometer (Wescor Vapro 5520). Series resistance was compensated by 60–70 %.
Liquid junction potential changes due to extracellular Cl− replacement were calculated with the Clampex10 software (Axon Instruments) and corrected for by V m = V test − 3.8 mV (EATC and HEK293 experiments) or V m = V test − 4.2 mV (ELA experiments) for I Cl, swell. A ramp protocol ranging from V test = −100 to +100 mV (EATC experiments) or V test = −80 to +80 mV (ELA experiments) over 1 s with a holding potential of V test = 0 mV was run continuously with 15 s intervals to follow the current activation. A step protocol with a holding potential, V hold = 0 mV and steps of 1 s duration ranging from V test = −100 to +100 mV with 20 mV increments was applied before and after hypotonic stimulation of I Cl, swell.
Cell volume measurements
Cell volume was measured by electronic cell sizing in a Beckman–Coulter Multisizer™ 3 (Beckman–Coulter, Copenhagen, Denmark). The tube orifice was 100 μm. Cell density was 20,000 cells/mL, equivalent to a cytocrit of 0.002 %. Mean cell volume was calculated as the median of the volume distribution curves after calibration with latex beads (nominal diameter 10 μm). Volume measurements were carried out in 37 °C isotonic Ringer’s solution (274 mOsmol/kg) for initial cell sizing of the control volume, and in 37 °C hypotonic Ringer’s solution (160 mOsmol/kg) for the RVD responses. Media used for cell volume measurements were filtered (Millipore filters, 0.45 mm) prior to experiments. Both Ringer’s solutions contained (in mM): Na+, 75; Cl−, 75; K+, 2.5; Mg2+, 0.5; Ca2+, 0.5; SO4 2−, 0.5; HPO4 2–, 0.5; MOPS, 3.3; TES, 3.3; HEPES, 5. The osmolality of the isotonic solution was adjusted using sucrose. For Ca2+-free experiments, CaCl2 was substituted by NaCl and EGTA was added to a concentration of 1 mM.
Taurine efflux measurements
ELA WT and KD cells were grown in 6-well plates to 80 % confluency. Before the start of the experiment, the cells were loaded with 3H-taurine (final concentration: 0.04 μM) and incubated for 2 h at 37 °C and 5 % CO2. After incubation, the cells were washed with an isotonic (300 mOsmol/kg) NaCl solution containing (in mM): NaCl, 143; KCl, 5; Na2HPO4, 1; CaCl2, 1; MgSO4, 1; HEPES, 10, and pH adjusted to 7.4. A volume of 1 mL of isotonic NaCl was added to each well at time zero, and every 2 min the solution in each well was transferred to a vial and replaced by either 1 mL fresh isotonic solution (0–8 min) or fresh hypotonic (200 mOsmol/kg) solution (10–24/30 min). The hypotonic solution was obtained by dilution of the isotonic solution with buffered water. Following the final removal of hypotonic solution, 1 mL of 1 M NaOH was added to each well to lyse the cells. The six-well plate was placed on a shaking table for a minimum of 1 h. The cell lysates were then transferred to vials; 1 mL ddH2O was added to each well and subsequently transferred to a vial (this was repeated twice); 3.5 mL Ultima Gold™ scintillation cocktail (PerkinElmer) was added to each vial and the vial was shaken thoroughly. 3H activity was measured using a beta-scintillation counter (Packard). Assuming that there is only one channel type facilitating the taurine release, and that taurine release follows a mono-exponential time course, the fractional rate constant (k) for taurine release in each time interval can be deduced from the following equation: A t = A t–Δt *e−k*Δt , where A t is the cellular activity of 3H-labeled taurine at the end of the given time interval (counts per minute), A t–Δt is the activity at the beginning of the interval (counts per min), k is the fractional rate constant (minutes), and Δt is the length of the interval (2 min). Rate constants for taurine release under isotonic conditions were estimated as the average of release rates at t = 8 min and t = 10 min, whereas the values for hypotonic conditions were estimated as the maximal transport rate after shift to hypotonic bath solution.
Caspase-3 activity assay
Caspase-3 activity was measured using the Fluorometric Homogenous Caspases Assay (Roche Applied Science). 10,000 ELA WT or KD cells per well were added to two 96-well plates. The two 96-well plates were identical and used for caspase-3 activity measurements and protein determination, respectively. The plates were incubated at 37 °C and 5 % CO2 for 24 h. The medium was then replaced by medium containing 10 μM cisplatin and the plates were incubated at 37 °C and 5 % CO2 for 24 h. In the plate used for protein determination, the cells were washed in PBS, and lysis buffer (10 mM Tris-Cl, 1 % SDS) was added. This plate was then incubated at -80 °C for 24 h and protein concentrations were determined using a colorimetric DC protein assay (Bio-Rad), a FLUOstar Optima plate reader (BMG Labtech), and a standard curve based on samples with known protein concentrations. The plate used for caspase-3 activity measurements was frozen (30 min at −80 °C) and thawed (45 min at RT) three times to promote cell lysis. DEVD-R110 and incubation buffer from the assay kit was added to the cells and the plate was covered in aluminum foil and incubated at 37 °C for 1 h. Fluorescence was then measured at 520 nm with an excitation wavelength of 485 nm using the FLUOstar Optima plate reader. The caspase-3 activity of each cell line was calculated as the mean of the measurements in either three or five wells and fluorescence from wells containing only growth medium, DEVD-R110 and incubation buffer was subtracted from the measurements to remove background fluorescence. The caspase-3 activities were then normalized to the measured protein concentrations. Finally, all results were normalized to the caspase-3 activity of WT cells that had not been exposed to cisplatin.
ANO-KD or ANO-expressing cells were compared with WT or mock-transfected cells using two-sided Student’s t tests assuming either equal or unequal variances depending on the result of an F test. The results were considered significant when p < 0.05.
I Cl, swell in mANO1, mANO6, or mANO10-transfected HEK293 cells and mANO6-transfected EATC
I Cl, swell in EATC and ELA cells with stable KD of ANO6
RVD in WT and ANO6-KD EATC
We then tested if ANO6, through its role as a CaCC, could contribute to RVD when extracellular Ca2+ was present. In this experiment, the ANO6-KD cells showed a significantly lower initial slope of 0.093 ± 0.01 min−1 (n = 14) when compared with 0.14 ± 0.01 min−1 (n = 8) in the WT cells (p = 0.012) (Fig. 3c). The recovery after 3 min in the ANO6-KD cells, 75.3 ± 6.5 % (n = 14), was also significantly lower compared with WT, 109.2 ± 5.2 % (n = 8; p = 0.002) (Fig. 3d). When looking at WT cells, the data show that removal of extracellular Ca2+ significantly reduces both the initial slope (p = 0.005) (Fig. 3c) and the recovery after 3 min (p = 0.015) (Fig. 3d), whereas removal of extracellular Ca2+ from ANO6-KD cells had no significant effect on neither the initial slope (p = 0.43) nor the recovery after 3 min (p = 0.56). These results suggest that Ca2+ plays an important role in RVD in EATC, and that this is, at least partly, due to the Ca2+-dependent activity of ANO6. This seems to contradict previous results from our group which showed that RVD in EATC does not depend on Ca2+ . However, the EATC investigated in our previous study was cultured in the abdominal cavity of female Naval Medical Research Institute mice, whereas EATC in the present study were cultured in RPMI-1640 medium. The most likely explanation is that the in vivo-generated cell line had a lower level of anoctamin expression. However, as this cell line is no longer available, a direct proof of this notion cannot be carried out.
Taurine efflux in WT and ANO1- and ANO16-KD ELA cells
Cisplatin-induced caspase-3 activity in WT and ANO6-KD ELA cells
ANO6 and the volume-activated anion current
It has previously been suggested that ANO6 is activated following cell swelling , and it could therefore be speculated that ANO6’s activity is volume regulated. In the present study, however, expression of mANO1, mANO6, or mANO10 in HEK293 cells and mANO6 in EATC, did not affect swelling-activated currents in the absence of intracellular Ca2+ (10 mM EGTA added to the pipette solution) (Fig. 1e). Moreover, KD of ANO6 in EATC and in ELA cells did not reduce the swelling-induced current (Fig. 2e, f). These results are showing that ANO6 as well as ANO1 and ANO10 do not contribute to cell volume-activated currents, which is in agreement with the results obtained by Shimizu et al. . This is not in conflict with the study by Almaca et al. who found that expression of ANO1 and ANO2 enhanced I Cl, swell in whole-cell patch clamp experiments with 0.1 μM-free Ca2+ in the pipette, and knock-down of ANO1, ANO6, ANO8, and ANO9 reduced I Cl, swell under the same conditions . They hypothesized that the anoctamin-mediated I Cl, swell was stimulated through an autocrine mechanism that involves swelling-induced ATP release, binding to the purinergic P2Y2 receptors with a subsequent increase in intracellular Ca2+. It follows that anoctamins’ role in I Cl, swell and RVD would be secondary to an increased intracellular (Ca2+).
ANO6 is involved in RVD in a Ca2+-dependent manner
EATC are well suited for the study of the putative role of anoctamin channels in RVD. It is the first cell type in which an increased Cl− permeability following hypotonic cell swelling was demonstrated , and the cell swelling-activated current as well as Ca2+-activated current are biophysically and pharmacologically well characterized in these cells . In a variety of cells, VRAC as well as CaCC are known to be associated with the RVD response . However, VRAC in ELA cells does not require Ca2+ for activation  (see also Figs. 1 and 2), whereas CaCCs are dependent on influx of Ca2+. To approach the question of whether ANO6 is swelling-activated per se, we investigated if ANO6 has a Ca2+-independent role in RVD by studying cell volume recovery in WT and ANO6-KD EATC in the absence of extracellular Ca2+. Our results show that there is no significant difference between WT and ANO6-KD cells in their ability to undergo RVD in Ca2+-free solution. Almaca et al. previously showed that ANO1, ANO6, ANO8, and ANO9 are essential for RVD in HEK293 cells and that I Cl, swell is reduced in the colonic epithelium and in salivary acinar cells from mice lacking expression of ANO1 [1, 18]. However, these experiments were conducted in the presence of extracellular Ca2+. Thus, neither their results nor their hypothesis mentioned above contradict our conclusion. To replicate their results with our protocol, we repeated our experiment in the presence of extracellular Ca2+. We observed that ANO6-KD cells display the RVD response, but it proceeds at a significantly slower rate compared with the response in WT cells (Fig. 3c, d). This result shows that ANO6 contributes to the physiological RVD in EATC, but only in the presence of Ca2+, i.e., under normal physiological conditions. In whole cell patch clamp studies, the high intracellular Ca2+ required for ANO6 activation is secured by the free Ca2+ concentration in the pipette, whereas in the RVD response of intact cells, the high intracellular Ca2+ at the submembrane domains governing ANO6 activation depends on a putative Ca2+ influx during RVD. Apparently, in our experiments, this influx was sufficient for driving Ca2+ above the threshold for activation of ANO6. The effect of cell swelling on Ca2+ i differs widely between cell types, as does the dependence of RVD on extracellular Ca2+. This is summarized and discussed in . The Ca2+ dependence of RVD is likely to reflect the involvement of Ca2+-activated K+ and/or Cl− channels.
ANO6 and ANO1 do not contribute to taurine efflux
Taurine is an essential organic osmolyte in most mammalian cells, and taurine release after cell swelling is an important component of the RVD response [12, 20]. Under isotonic conditions, taurine release is low and the mechanism behind it is unknown . After hypotonic exposure, the VSOAC is activated, allowing taurine efflux to drastically increase [11, 12]. VSOAC has not been identified at the molecular level and was previously considered to be the same as VRAC. However, evidence now indicates that they are distinct channels . As anoctamins are involved in RVD, we speculated if they were taurine channels. We therefore investigated the effects of ANO1- and ANO6-KD on taurine efflux under isotonic and hypotonic conditions. Our results clearly show that swelling-induced taurine release is not reduced by ANO-KD, i.e., ANO1 and ANO6 are different from VSOAC (Fig. 4b). In some KD clones, we observed a small but significant increase in taurine efflux compared with WT under isotonic conditions. This might be explained by a compensatory mechanism in which taurine release is increased to compensate for the lacking anoctamin activity.
ANO6 is involved in cisplatin-induced apoptosis in ELA cells
AVD has been shown to be both necessary and sufficient to initiate apoptosis in some cell types [7, 8, 22]. AVD is very similar to RVD in many respects and several ion channels, including ANO1 and VRAC, are involved in both processes [1, 26, 29]. We therefore investigated if ANO6 is involved in apoptosis. Our results show that ANO6 plays an important role during cisplatin-induced apoptosis in ELA cells (Fig. 5). This is similar to what Martins et al. found in A549 cells , but in contradiction to the findings of Shimizu et al., who showed that KD of ANO6 does not affect staurosporine-induced AVD in HeLa cells . However, a previous study from our group showed that the subset of ion channels activated following apoptotic stimuli can vary considerably between cell lines , and it is therefore quite possible that ANO6 only contributes to apoptosis in some cell types. With respect to RVD, we showed that influx of Ca2+ was required for ANO6 to play a role in RVD. It is likely that the same is true for AVD, i.e. only in cells where an early influx of Ca2+ is seen there will be a contribution of ANO6 to the AVD process.
Our whole-cell patch clamp data demonstrate that ANO6-dependent Cl− currents, unlike VRAC currents, are not activated by osmotic cell volume increase in the absence of Ca2+ in the pipette. However, there may be not-yet-described compensatory interactions between ANO6 and VRAC, as the latter tend to increase its activity in the absence of ANO6. Furthermore, we show that ANO6 plays a role in RVD provided there is Ca2+ in the bath, once again confirming the central role of Ca2+ in opening of ANO6 channels. Finally, we find that ANO6-KD reduces cisplatin-induced apoptosis in ELA cells, suggesting that ANO6 contributes to AVD.
Arne Nielsen and Birthe J. Hansen are acknowledged for excellent technical assistance and Louise Lindbæk for performing western blots for Fig. 2d. The following authors’ current work addresses differ from the affiliation line: Christian A. Juul (Department of Micro- and Nanotechnology, Technical University of Denmark), Søren Grubb (Biomedical Institute, Faculty of Health Sciences, University of Copenhagen), Kristian A. Poulsen (Køge Gymnasium, DK-4600 Køge, Denmark), Tania Kyed (Andreasen and Elmgaard, DK-2730 Herlev, Denmark) and Nadia Hashem (Department of International Health, Immunology and Microbiology, University of Copenhagen).
The present work was supported by The Danish Council for Independent Research/Natural Sciences (Grants 09-064182, and 10-085373), Lundbeck Foundation (J Nr R32-A3102), and Carlsberg Foundation (2008-01-0639).
Apoptotic volume decrease
Calcium-activated chloride channel
Ehrlich ascites tumor cell
Human embryonic kidney
Regulatory volume decrease
Volume-regulated anion channel
Volume-sensitive organic osmolyte and anion channel
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