kca3 1  (Bioss)

Journal: bioRxiv

Article Title: Cell crowding induces TRPV4 inhibition and its relocation to plasma membranes, implicating pro-invasive cell volume reduction mechanotransduction pathway

doi: 10.1101/2024.07.05.602223

Figure Lengend Snippet: Various ion channels are relocated to the plasma membrane under cell crowding conditions. (A) We used the plasma membrane marker DiIC18(3) to confirm the association of TRPV4 with the plasma membrane in MCF10DCIS.com and MCF10CA1a cells under OC conditions. As described in the Methods section, we stained DiIC18(3) in live cells and co-stained TRPV4 and DAPI in fixed and permeabilized cells. The IF images show TRPV4 (red), DiIC18(3) (DiI, green), and DAPI (blue). The line profile plots on the right demonstrate colocalization of TRPV4 with DiIC18(3) at the plasma membrane (PM), marked by the green DiIC18(3) signal, which overlaps with the red TRPV4 signal. The nucleus location (NUC) is indicated by the blue DAPI signal. Scale bar = 20 μm. (B) We examined the relocation of KCNN4 and PIEZO1 to the plasma membrane in response to cell crowding. Mass spectrometry showed a slight increase in KCNN4 at the plasma membrane under OC conditions. In ND MCF10DCIS.com cells, KCNN4 was predominantly cytosolic, whereas PIEZO1 showed some plasma membrane association. Under OC conditions, both KCNN4 and PIEZO1 showed a modest relocation to the plasma membrane. (C) Line analysis confirmed a slight increase in plasma membrane association for both KCNN4 and PIEZO1 under OC conditions compared to ND conditions. Scale bar = 20 μm. For the statistical analysis, we employed a nonparametric approach using the Mann-Whitney test with a two-tailed p-value. The levels of statistical significance are denoted as follows: **** indicates p < 0.0001, *** indicates p < 0.001, * indicates p < 0.1, and “ns” indicates p > 0.05.

Article Snippet: The primary antibodies used were TRPV4 (Abcam 39260; 1:500 dilution), TfR (ThermoFisher Scientific 13-6800; 1:500 dilution), Piezo1 (Alomone APC-087; 1:500), and KCNN4 (Alomone ALM-051; 1:500).

Techniques: Membrane, Marker, Staining, Mass Spectrometry, MANN-WHITNEY, Two Tailed Test

Journal: bioRxiv

Article Title: Cell crowding induces TRPV4 inhibition and its relocation to plasma membranes, implicating pro-invasive cell volume reduction mechanotransduction pathway

doi: 10.1101/2024.07.05.602223

Figure Lengend Snippet: (A) Using the Fluo-4 assay, we observed an initial calcium spike (marked as “Rise”) in ND MCF10DCIS.com cells in response to 74.4 mOsmol/kg PEG 300, due to osmotic water outflow. This was followed by a homeostatic relaxation, aimed at restoring calcium levels, which likely involved the inhibition of ion channels like TRPV4, leading to their plasma membrane relocation. Scale bars = 20 μm. (B) The same hyperosmotic condition (74.4 mOsm/Kg PEG 300 for 15 min) led to the relocation of KCNN4 and PIEZO1 to the plasma membrane, similar to the relocations observed under OC conditions. Line analysis results showed the relative relocations of each channel in response to hyperosmotic (PEG) and cell crowding (OC) stresses, compared to ND conditions.

Article Snippet: The primary antibodies used were TRPV4 (Abcam 39260; 1:500 dilution), TfR (ThermoFisher Scientific 13-6800; 1:500 dilution), Piezo1 (Alomone APC-087; 1:500), and KCNN4 (Alomone ALM-051; 1:500).

Techniques: Inhibition, Membrane

Journal: PNAS Nexus

Article Title: The SK4 channel allosteric blocker, BA6b9, reduces atrial fibrillation substrate in rats with reduced ejection fraction

doi: 10.1093/pnasnexus/pgae192

Figure Lengend Snippet: BA6b9 treatment reduces the AF substrate of post-MI rats. A) Confirmatory in vitro recordings. Left: Representative trace of WT SK4 currents in the absence and presence of 20 µM BA6b9, displaying a degree of inhibition of ≈56%. Right: Representative traces of an inside-out macropatch from a CHO cell expressing WT SK4 channels in the absence and presence of 10 µM BA6b9 under internal saturating calcium concentrations. Currents were recorded by 10 repetitive 1 s duration voltage ramps from −100 mV to +100 mV from a holding potential of 0 mV. B) BA6b9 treatment significantly reduced AF induction and AF duration. C) Example of postburst AF episodes in the vehicle (left) and BA6b9 (right) groups. D) Mean power spectrum of the AF episodes following long-term BA6b9 vs. vehicle treatment. Notably, the vehicle group demonstrated greater amplitudes over a wide range of frequencies relative to the BA6b9 group. Notch (arrow) indicates the zone where a notch filter was applied due to power supply-related noise (50 Hz). E) Quantitative analysis of delta between the power spectrum integrals of arrhythmic episodes and preburst NSR. Note the significantly higher values in the vehicle group compared to the AF events among BA6b9-treated rats.

Article Snippet: Antigen retrieval was performed using BOND Epitope Retrieval Solution 1 (Citrate buffer, prediluted, pH 6.0) for 20 min at 100°C, followed by peroxide treatment for 10 min. For membranal staining, we primarily incubated the sections with WGA (29022, CF488 WGA, Biotium, 1:500 in PBS) conjugated with Alexa Fluor 488 for 30 min, followed by incubation with blocking buffer (10% normal goat serum, 0.1% Triton, and 10% bovine serum albumin) for 30 min. For analyses of SK4 expression and localization, we incubated the specimens with the primary antibody (ALM-051, Alomone Labs, mouse monoclonal antibody against the 3rd extracellular loop of human SK4, 1:50) for 90 min and then stained with a Cy3-conjugated secondary antibody (711-165-151, Jackson Immunoresearch Laboratories, Cy TM 3-conjugated AffiniPure Donkey Anti-Mouse, 1:100) for 90 min. For Cx43 expression and localization analyses, we incubated the specimens with the primary antibody (C6219, Sigma-Aldrich, rabbit polyclonal antibody against the C-terminus of human/rat Cx43, 1:400) for 90 min and stained with a Cy5-conjugated secondary antibody (711-175-152, Jackson Immunoresearch Laboratories, Cy TM 5-conjugated AffiniPure Donkey Anti-Rabbit, 1:200) for 90 min. At the end of the staining, we incubated the specimens with Vector TrueVIEW Autofluorescence Quenching kit (SP-8400-15, Vector laboratories) for 10 min to improve the signal-to-noise ratio and reduce autofluorescence.

Techniques: In Vitro, Inhibition, Expressing

Journal: PNAS Nexus

Article Title: The SK4 channel allosteric blocker, BA6b9, reduces atrial fibrillation substrate in rats with reduced ejection fraction

doi: 10.1093/pnasnexus/pgae192

Figure Lengend Snippet: Effect of BA6b9 on SK4 expression in the left atrium of rats with MI-induced HF. A) Statistical summary of overall left-atrial SK4 expression; vehicle- vs. BA6b9-treated rats, compared to control ( n = 7, n = 8, n = 4, respectively; one-way ANOVA, F(2, 16) = 14.27, Sidak's multiple comparisons test P = 0.0003). B1) Representative histological LA cross-section from a control rat (upper left), stained with DAB. B2, B3) Representative DAB-stained histological cross-sections of the LA from post-MI rats treated with vehicle (upper right) or BA6b9 (lower left) for 21 days. Brown staining intensity indicates the level of SK4 expression in the tissue, with darker brown indicating stronger expression. B4) Negative control SK4 staining. An inset in each photograph shows the full LA tissue in low resolution.

Article Snippet: Antigen retrieval was performed using BOND Epitope Retrieval Solution 1 (Citrate buffer, prediluted, pH 6.0) for 20 min at 100°C, followed by peroxide treatment for 10 min. For membranal staining, we primarily incubated the sections with WGA (29022, CF488 WGA, Biotium, 1:500 in PBS) conjugated with Alexa Fluor 488 for 30 min, followed by incubation with blocking buffer (10% normal goat serum, 0.1% Triton, and 10% bovine serum albumin) for 30 min. For analyses of SK4 expression and localization, we incubated the specimens with the primary antibody (ALM-051, Alomone Labs, mouse monoclonal antibody against the 3rd extracellular loop of human SK4, 1:50) for 90 min and then stained with a Cy3-conjugated secondary antibody (711-165-151, Jackson Immunoresearch Laboratories, Cy TM 3-conjugated AffiniPure Donkey Anti-Mouse, 1:100) for 90 min. For Cx43 expression and localization analyses, we incubated the specimens with the primary antibody (C6219, Sigma-Aldrich, rabbit polyclonal antibody against the C-terminus of human/rat Cx43, 1:400) for 90 min and stained with a Cy5-conjugated secondary antibody (711-175-152, Jackson Immunoresearch Laboratories, Cy TM 5-conjugated AffiniPure Donkey Anti-Rabbit, 1:200) for 90 min. At the end of the staining, we incubated the specimens with Vector TrueVIEW Autofluorescence Quenching kit (SP-8400-15, Vector laboratories) for 10 min to improve the signal-to-noise ratio and reduce autofluorescence.

Techniques: Expressing, Control, Staining, Negative Control

Journal: PNAS Nexus

Article Title: The SK4 channel allosteric blocker, BA6b9, reduces atrial fibrillation substrate in rats with reduced ejection fraction

doi: 10.1093/pnasnexus/pgae192

Figure Lengend Snippet: Effect of BA6b9 on collagen deposition, α-SMA expression, and SK4 expression in the LA epicardium of rats with MI-induced HF. A) Statistical summary of LA epicardial fibrosis (analysis of six randomized epicardial fields for each atrial section, total of 18 atrial-epicardium fields per animal); vehicle- vs. BA6b9-treated rats, compared to control ( n = 7, n = 8, n = 4, respectively; one-way ANOVA, F(2, 16) = 16.53, Sidak's multiple comparisons test P = 0.0001). A1) Representative histological cross-section of LA myocardium attached to the epicardial tissue from a control rat (left upper row). The analyzed area is marked by dashed lines. A2, A3) Representative histological cross-sections of the LA from post-MI rats treated with vehicle (left middle row) or BA6b9 (left lower row) for 21 days. Sections A1–A3 were stained with Masson's Trichrome. B) Statistical summary of LA epicardial α-SMA expression; (analysis: same as in A; vehicle vs. BA6b9-treated rats, compared to control ( n = 7, n = 8, n = 4, respectively; one-way ANOVA, F(2, 16) = 16.53, Sidak's multiple comparisons test P = 0.0001). B1) Representative histological cross-section of LA myocardium attached to the epicardial tissue from a control rat (middle upper row). B2, B3) Representative histological cross-sections of the LA in post-MI rats treated with vehicle (center) vs. BA6b9 (middle lower row) for 21 days. Sections B1–B3 were stained with Sirius Red. C) Statistical summary of LA epicardial α-SMA expression; (analysis: same as in A; vehicle- vs. BA6b9-treated rats, compared to control ( n = 7, n = 8, n = 4, respectively; one-way ANOVA, F(2, 16) = 10.21, Sidak's multiple comparisons test P = 0.0014). C1) Representative histological cross-section of LA myocardium attached to the epicardial tissue from a control rat (right upper row). C2, C3) Representative histological cross-sections of the LA in post-MI rats treated with vehicle (right middle row) or BA6b9 (right lower row) for 21 days. Sections C1–C3 were stained with DAB. Note the marked thickening of the atrial epicardium in MI rats compared to controls as well as the significant reductions in collagen deposition (A, A1–A3), α-SMA expression (B, B1–B3), and SK4 expression (C, C1–C3) in the BA6b9-treated rats compared to the vehicle group. An inset in each photograph shows the full LA tissue in low resolution.

Article Snippet: Antigen retrieval was performed using BOND Epitope Retrieval Solution 1 (Citrate buffer, prediluted, pH 6.0) for 20 min at 100°C, followed by peroxide treatment for 10 min. For membranal staining, we primarily incubated the sections with WGA (29022, CF488 WGA, Biotium, 1:500 in PBS) conjugated with Alexa Fluor 488 for 30 min, followed by incubation with blocking buffer (10% normal goat serum, 0.1% Triton, and 10% bovine serum albumin) for 30 min. For analyses of SK4 expression and localization, we incubated the specimens with the primary antibody (ALM-051, Alomone Labs, mouse monoclonal antibody against the 3rd extracellular loop of human SK4, 1:50) for 90 min and then stained with a Cy3-conjugated secondary antibody (711-165-151, Jackson Immunoresearch Laboratories, Cy TM 3-conjugated AffiniPure Donkey Anti-Mouse, 1:100) for 90 min. For Cx43 expression and localization analyses, we incubated the specimens with the primary antibody (C6219, Sigma-Aldrich, rabbit polyclonal antibody against the C-terminus of human/rat Cx43, 1:400) for 90 min and stained with a Cy5-conjugated secondary antibody (711-175-152, Jackson Immunoresearch Laboratories, Cy TM 5-conjugated AffiniPure Donkey Anti-Rabbit, 1:200) for 90 min. At the end of the staining, we incubated the specimens with Vector TrueVIEW Autofluorescence Quenching kit (SP-8400-15, Vector laboratories) for 10 min to improve the signal-to-noise ratio and reduce autofluorescence.

Techniques: Expressing, Control, Staining

Journal: Molecular Medicine Reports

Article Title: M2 macrophage‑derived exosomes alleviate KCa3.1 channel expression in rapidly paced HL‑1 myocytes via the NF‑κB (p65)/STAT3 signaling pathway

doi: 10.3892/mmr.2024.13179

Figure Lengend Snippet: Electricity of KCa3.1 was measured using a whole cell clamp in different groups. (A) Membrane currents were recorded with the protocol shown in the inset of the HL-1 myocytes in different groups before and after application of TRAM-34 (1 µmol/l). (B) Current-voltage relationships of TRAM-34-sensitive current mean values derived by digitally subtracting the current before TRAM-34 application from the current after TRAM-34 application. (C) Current density of KCa3.1 in each group. Data are presented as the mean ± SEM (n=5). **P<0.01, ***P<0.001 and ****P<0.0001. PDTC, pyrrolidine dithiocarbamate; NC, negative control.

Article Snippet: The primary antibodies used were F4/80 (1:100; cat. no. 28463-1-Ap; Proteintech Group, Inc.), CD206 (1:75; cat. no. GB113497; Wuhan Servicebio Technology Co., Ltd.), KCa3.1 (1:100; cat. no. bs-6675r; BIOSS) and NF-κB (p-p65; 1:100; cat. no. cy6367; Shanghai Abways Biotechnology Co., Ltd.).

Techniques: Membrane, Derivative Assay, Negative Control

Journal: Molecular Medicine Reports

Article Title: M2 macrophage‑derived exosomes alleviate KCa3.1 channel expression in rapidly paced HL‑1 myocytes via the NF‑κB (p65)/STAT3 signaling pathway

doi: 10.3892/mmr.2024.13179

Figure Lengend Snippet: Western blot analysis is used to determine the levels of KCa3.1, p-p65, STAT3, IL-1β and KCa3.1 in several groups and immunofluorescent double staining is used to measure the expression of KCa3.1 and p-p65. (A) Representative gel bands depicting the expression of different proteins using specific antibodies. GAPDH was used as the loading control. (B-E) Protein levels of KCa3.1, p-p65, STAT3 and IL-1β. (F) Immunofluorescence double staining of p-p65 (red) and KCa3.1(green) in different groups (n=3). Scale bars, 100 µm. (G) The mean fluorescence intensities of KCa3.1 and p-p65 were measured using ImageJ software. Data are presented as the mean ± SEM, and analyzed by one-way ANOVA followed by Tukey's multiple comparisons test (n=3). *P<0.05, **P<0.01, ***P<0.001 and ****P<0.0001. p-, phosphorylated; PDTC, pyrrolidine dithiocarbamate; NC, negative control.

Article Snippet: The primary antibodies used were F4/80 (1:100; cat. no. 28463-1-Ap; Proteintech Group, Inc.), CD206 (1:75; cat. no. GB113497; Wuhan Servicebio Technology Co., Ltd.), KCa3.1 (1:100; cat. no. bs-6675r; BIOSS) and NF-κB (p-p65; 1:100; cat. no. cy6367; Shanghai Abways Biotechnology Co., Ltd.).

Techniques: Western Blot, Double Staining, Expressing, Control, Immunofluorescence, Fluorescence, Software, Negative Control