In the present study, the Trpc6 knockout (Trpc6^−/−) mice (C57BL/6J) were obtained by Suzhou Cyagen Biosciences (Suzhou) Inc. The genotype of Trpc6^−/− homozygous mice was determined by PCR amplification and agarose gel electrophoresis separation (Fig. S1). WT mice were obtained from the same litter of Trpc6^−/− mice. The mice were bred in an environmentally controlled room (temperature, 22–24°C; relative humidity, 50–60%) under a 12-h light/dark cycle with unlimited access to food and water. After the acclimatization of 50 male mice (20–25 g) at 8 weeks of age, they were divided into five groups: WT, Trpc6^−/−, WT + high fat diet (HFD) + streptozotocin (STZ), Trpc6^−/− + HFD and Trpc6^−/− + HFD + STZ (n=10 per group). The mice of the WT and Trpc6^−/− groups were fed with a growth-maintenance diet and the other mice were given a HFD of 20% carbohydrates, 20% protein and 60% fat (cat. no. D12492, Jiangsu Xietong Pharmaceutical Bio-engineering Co., Ltd.) for eight weeks.

After eight weeks, the mice of the WT + HFD + STZ and Trpc6^−/− + HFD + STZ groups (fasting without water restriction for 8 h) were treated intraperitoneally with STZ (110 mg/kg, Shanghai Yuanye Bio-Technology Co., Ltd.), which was dissolved in a 0.1 M sodium citrate buffer to induce the T2DM model (27). The fasting blood glucose (FBG) level was measured after 72 h. Mice with a FBG concentration ≥16.7 mM were considered optimal for further experiments. Next, each group was given the same diet as described previously for eight weeks. The health and behavior of the animals were monitored daily. Throughout the experiment, one mouse in the Trpc6^−/− + HFD + STZ group succumbed to infection at week 13 and one mouse in the WT + HFD + STZ group succumbed to hyperglycemia at weeks 13 and 14, respectively. The remaining mice were sacrificed. The mice were anesthetized using an intraperitoneal (IP) injection of tribromoethanol (300 mg/kg) and sacrificed by cervical dislocation after orbital blood extraction (once; ~0.2 ml) when they did not respond to gentle stimulation. All experiments were conducted under the approval of the Anhui Medical University Ethics Committee (approval no. LLSC20190302). When a click in the neck of the mouse was clearly heard, i.e., cervical spine detachment, spinal cord rupture and the heartbeat of the mouse stopped and the spontaneous respiration ceased it was considered that the mouse was dead and both kidneys were quickly removed. One kidney was fixed with paraformaldehyde (4%) for histological examination and the other was placed at −80°C for western blot analysis.

The body weight and FBG levels were observed to evaluate the T2DM model. The body weight (n=8-10) was measured once every two weeks. The FBG levels were measured every two weeks from 8–16 weeks by using a portable blood glucose meter (Sinocare Inc.). The test was performed using a second drop of blood from the tail vein, the total blood volume being ~40 µl. Following the sacrifice of the mice, the serum creatinine (SCR) and blood urea nitrogen (BUN) were measured using urea assay kit and creatinine assay kit (Nanjing Jiancheng Bioengineering Institute; cat. nos. C013-2-1 and C011-2-1). At 16 weeks, the 24 h urine samples were collected and kits used as follows: the urinary albumin level (cat. no. C035-2-1), serum total cholesterol (TC; cat. no. A111-1-1), triglyceride (TG; cat. no. A110-1-1), free fatty acids (FFA; cat. no. A042-2-1), low density lipoprotein (LDL-C; no. A113-1-1) and high-density lipoprotein (HDL-C; cat. no. A112-1-1) (all Nanjing Jiancheng Bioengineering Institute). All kit procedures were conducted strictly according to the manufacturer instructions.

The morphological examination of the kidneys was performed using hematoxylin and eosin (H&E), periodic acid-Schiff (PAS; Beijing Solarbio Science & Technology Co., Ltd.; cat. no. G1208) and Masson's trichrome staining (Beijing Solarbio Science & Technology Co., Ltd.; cat. no. G1340) methods. H&E staining was conducted to observe the pathological changes of the kidney (28). Briefly, the kidneys (n=4) were fully fixed with paraformaldehyde (4%) at 4°C for 24 h, dehydrated and embedded in paraffin, then cut into 5-µm thick sections. The kidney sections were deparaffinized in xylene and rehydrated in graded alcohol series (anhydrous ethanol, 85% ethanol and 75% ethanol), and then stained with hematoxylin for 4 min and eosin for 35 sec at room temperature (RT). After being rinsed with running water, the tissues were sealed using neutral resin and were imaged using an Intelligent Tissue Section Imaging System (3DHISTECH, Ltd.) to observe renal histopathological changes. Renal injury was scored in a blinded manner with the following scoring criteria: no injury=0; <25%=1; 25–50%=2; 50–75%=3; and >75%=4.

Masson's staining was performed to observe tissue fibrosis (29). For Masson staining, the paraffin sections (n=4) were first dewaxed, hydrated and stained with hematoxylin for 4 min, then underwent acidic ethanol fractionation for 15 sec and were stained with Masson's blue solution for 5 min. This was followed by fuchsin staining for 9 min, phosphomolybdic acid for 3 min, then aniline blue staining for 6 min. All steps were performed at RT. The sections were then sealed using neutral resin and imaged using the Intelligent Tissue Section Imaging System (3DHISTECH, Ltd.). Finally, the mean density of Masson staining from five random areas (magnification, ×400) per section was analyzed by the Image-pro Plus 6.0 image software (Media Cybernetics, Inc.) to evaluate renal fibrosis.

PAS staining was further performed to measure the disposition of acidic glycoproteins in order to assess renal injury (30). The renal paraffin sections (n=4) were dewaxed and hydrated, then stained in the Schiff solution for 8 min and the hematoxylin solution for 1 min at RT. The sections were sealed using neutral resin. The results of PAS-staining were imaged with the Intelligent Tissue Section Imaging System (3DHISTECH, Ltd.). The positive areas were purplish red and the cell nuclei were blue. To evaluate the extent of renal fibrosis, the mean intensity of positive mesangial cells and the ratio of mesangial area to glomerular (%) from five random areas (magnification, ×400) per section were analyzed by the Image-Pro Plus 6.0 software (Media Cybernetics, Inc.).

Dihydroethidium (DHE) was used to measure ROS production (31). Briefly, mice (n=3) were injected via the tail vein with DHE (0.1 ml/10 g, 100 µM; Beyotime Institute of Biotechnology). The mouse was euthanized by cervical dislocation after 30 min and the kidneys were quickly removed and embedded in OCT composite media (Sakura Finetek USA, Inc.) at −20°C for 1 h. The renal tissue was sectioned at 10 µm using a cryostat (CM3050; Leica Microsystems GmbH) and the sections rinsed three times with PBS buffer and stained with Hoechst solution (5 mg/l; MilliporeSigma) at RT for 5 min. The section was washed and sealed with an anti-fluorescent quenching agent, then imaged using the Intelligent Tissue Section Imaging System (3DHISTECH, Ltd.). Finally, the fluorescence intensity from three random areas (magnification, ×400) per section was examined using the Image-Pro Plus software (Media Cybernetics, Inc.) to detect the levels of ROS production.

The β-Gal activity was examined by β-Gal staining for senescence-associated injury. The frozen sections (n=3) were first warmed to RT, allowed to dry slightly, fixed with the β-Gal fixative (Beyotime Institute of Biotechnology) for 15 min, then washed three times with PBS. The PBS was then discarded and the β-Gal staining working solution was added to the sections for incubation at 37°C overnight. The staining solution was then discarded, rinsed three times with PBS and imaged using the Intelligent Tissue Section Imaging System (3DHISTECH, Ltd.). Finally, the mean density (blue) from three random areas (magnification, ×400) per tissue was examined with the Image-Pro Plus software (Media Cybernetics, Inc.) to estimate β-Gal activity.

The 5 µm paraffin sections of kidney tissue (n=4) were dewaxed and rehydrated. For antigen retrieval, the section was heated using a microwave oven for 8 min in sodium citrate buffer, stopped for 7 min, then reheated for 8 min. The section was then incubated in H₂O₂ (3%) at RT for 30 min to block endogenous peroxidase and then sealed with blocking solution at RT for 1 h. The sections were incubated in rabbit polyclonal antibodies (Table SI) at 4°C overnight. The sections were rinsed with PBS and incubated with polymer-coupled peroxidase-labeled goat anti-rabbit IgG at RT for 1 h, then the section was stained with a DAB kit and hematoxylin. Finally, at the end of the light-protected sealing, the sections were imaged by the Intelligent Tissue Section Imaging System (3DHISTECH, Ltd.). The mean intensity from five random renal cortex regions (magnification, ×400) per tissue was quantified by Image-Pro Plus software (Media Cybernetics, Inc.) to assess the expression of fibronectin (FN) and collagen IV (COL4).

Total proteins from renal cortexes (n=4) were isolated by the RIPA lysates buffer (cat. no. P0013B; Beyotime Institute of Biotechnology) in a fully automated sample freeze grinder (Shanghai Jingxin Industrial Development Co., Ltd.). After lysing for 30 min on ice, the tissue lysate was centrifuged (12,000 × g) at 4°C for 20 min to extract the supernatant. The protein concentration was determined using a BCA assay kit, and then the protein (20 µg) was separated on 10% gels using SDS-PAGE and transferred onto PVDF membranes. Next, the membrane was blocked with the 5% defatted milk at RT for 1 h and was incubated in the primary antibodies (Table SI) at 4°C overnight. The membrane was then washed three times in TBS with 0.05% Tween-20 (TBST) and was incubated in the corresponding secondary antibodies of goat anti-mouse IgG (cat. no. S0002; Affinity Biosciences; 1:10,000) or goat anti-rabbit IgG (cat. no. S0001; Affinity Biosciences; 1:10,000) for 1 h at RT. After being rinsed in TBST three times, the Western ECL kit (Bio-Rad Laboratories, Inc.) was applied to visualize the results and the Chemi Imaging System (Q4800 mini, Bioshine Chemi) was used to image the bands. The intensity of protein bands was measured by an image J v1.53 software (National Institutes of Health). The results were normalized to β-actin to indicate the change in target protein.

Briefly, the renal cortex specimen was sectioned into 1 mm³ pieces and transferred to 2.5% glutaraldehyde at 4°C for 2 h (n=3). After washing with PBS, the tissues were fixed with osmium tetroxide (1%) at RT for 2 h and embedded in Epon 812 for 12 h at 45°C, and then heated at 72°C for 24 h after dehydration. Ultrathin sections (70 nm) were sliced with an ultra-microtome (Leica UC7; Leica Microsystems GmbH). The section was double stained using lead citrate (stained for 30 min at RT) and uranyl acetate (stained at 4°C overnight before embedding). Ultrastructural images were taken by a transmission electron microscope (HT7700; Hitachi High-Technologies Corporation). Glomerular ultrastructural damage was determined by observing the glomerular mesangial and foot processes.

The human mesangial cell (HMC) line was purchased from the Modern Analysis and Testing Center of Central South University. The HMC line was cultured with DMEM medium containing 10% FBS (Zhejiang Tianhang Biotechnology Co., Ltd.) and placed in a 37°C incubator. The HMCs were divided into four groups: control, high glucose (HG; 25 mM) + palmitic acid (PA; 200 µM), vector + HG + PA and TRPC6-siRNA + HG + PA. The sequences of the short interfering RNAs (siRNAs) were: TRPC6 siRNA sense, 5′-GAGCAUCAUUGACGCAAAUTT-3′ and antisense, 5′-AUUUGCGUCAAUGAUGCUCTT-3′; and negative control siRNA sense, 5′-UUCUCCGAACGUGUCACGUTT-3′ and antisense, 5′-ACGUGACACGUUCGGAGAATT-3′. First, the cells were cultured in the dishes (35 mm) for 24 h and then transfected with Lipofectamine™ 2000 (Thermo Fisher Scientific, Inc.) with an empty vector or siRNA for 48 h at 37°C according to the manufacturer's instructions. After treatment with PA and/or HG for 24 h, the HMCs were incubated in a Fura-2 AM dye solution with F-127 for 20 min at 37°C and rinsed with an extracellular solution three times. The fluorescence density was detected every 3 sec under alternating excitation at 340 and 380 nm (F340 and F380) using a Digital Calcium Imaging Analysis Platform (IX73, DG-4PLUS/OF30; Olympus Corporation). The ratio (F340/F380) was measured with extracellular Ca²⁺ (1 mM) for 300 sec to estimate the basal level of [Ca²⁺]_i. Then, the BAPTA (1 mM, MedChemExpress), a calcium chelator, or 2 mM CaCl₂ were added into the extracellular solution and the Δ ratio (F340/F380) was used to estimate the change of calcium homeostasis after BAPTA or high calcium stimulation. The experiment was repeated three times independently.

Nile red staining was used to evaluate the production of lipids in the tissue sections. All steps were performed at room temperature. The frozen sections (n=3) were incubated in Nile red dilution (1 µg/ml) for 20 min. After rinsing three times, the sections were stained using Hoechst33258 for 4 min and were sealed using an anti-fluorescence quencher. All steps were performed at RT. The sections were imaged by the Intelligent Tissue Section Imaging System (3DHISTECH, Ltd.). The red fluorescence intensity from three renal cortex regions (magnification, ×400) per section was quantified using Image-Pro Plus software (Media Cybernetics, Inc.) to evaluate the lipid production in mouse kidney cortical regions.

The experimental results in the present study are shown as mean ± SD of ≥3 independent experiments. For statistical analysis, the data was analyzed using the GraphPad Prism 9.0 statistical software (GraphPad; Dotmatics). Data from each group were analyzed first by one-way ANOVA, then the difference between the two groups was performed by Tukey's test. P<0.05 was considered to indicate a statistically significant difference.

The results revealed that body weight increased slowly in both WT and Trpc6^−/− groups, suggesting that Trpc6 knockout had no obvious influence on body weight of normal mice. However, in Trpc6^−/− + HFD mice, body weight significantly increased from 2–16 weeks compared with the WT control mice (Fig. S2A; P<0.01). The T2DM mice showed significant weight loss in both WT + HFD + STZ and Trpc6^−/− + HFD + STZ groups after STZ injection, compared with the WT mice (Fig. S2A; P<0.01). Compared with the WT + HFD + STZ mice, Trpc6 knockout visibly delayed body weight loss (Fig. S2A; P<0.01) in Trpc6^−/− T2DM mice. The FBG results indicated that the FBG was raised in the Trpc6^−/− + HFD mice compared with the WT control mice, but within the normal range. After STZ modeling, the FBG levels were raised in both WT + HFD + STZ and Trpc6^−/− + HFD + STZ mice compared with the WT mice (Fig. S2B; P<0.01). However, compared with the WT + HFD + STZ mice, Trpc6 knockout decreased the FBG levels (Fig. S2B; P<0.01) in T2DM mice, but the levels were still >20 mM. Additional renal function indexes showed that the levels of BUN, SCR and urine protein were clearly raised in WT + HFD + STZ mice compared with the WT mice (Fig. S2C-E; P<0.05 or P<0.01); however, compared with the WT + HFD + STZ mice, knockout Trpc6 markedly decreased the levels of BUN, SCR and urine protein in T2DM mice (Fig. S2C-E; P<0.05). Furthermore, HFD-treatment alone had no influence on renal function in Trpc6^−/− mice compared with the WT control mice. The results revealed that Trpc6 knockout significantly improved renal function, but had only a weak hypoglycemic effect in T2DM mice.

The present study further evaluated the change of lipid metabolism-related parameters of FFA, TC, TG, LDL-C and HDL-C in serum and FFA in renal tissue. The results showed no significant difference in these parameters in Trpc6^−/− mice compared with the WT mice, indicating that knockout Trpc6 had no influence on lipid metabolism in normal mice. However, the levels of these parameters, were markedly raised in the WT + HFD + STZ mice, with the exception of HDL-C (Fig. S2F-K; P<0.05 or P<0.01). Compared with WT + HFD + STZ mice, Trpc6 knockout clearly decreased the levels of TG, TC and LDL-C (Fig. S2F, J and I; P<0.05 or P<0.01) but there was no statistical difference in HDL-C and FFA in T2DM mice. The data indicated that Trpc6 knockout may ameliorate blood lipid metabolism, but had no effect on FFA in renal tissues of T2DM mice.

The present study further explored renal injury by using H&E staining, immunoblotting and PAS staining in Trpc6^−/− T2DM mice. The H&E staining indicated that there was no obvious renal injury in WT, Trpc6^−/− and Trpc6^−/− + HFD group non-T2DM mice. When compared with the WT mice, the renal tissue showed evident damages in WT + HFD + STZ mice; the glomerular mesangial cells were expanded and proliferated and a number of renal tubular cells were vacuolated and detached. However, these pathological changes were improved in Trpc6^−/− + HFD + STZ mice (Fig. 1A and B; P<0.05). The present study further evaluated the biomarker, kidney injury molecule-1 (KIM-1), by western blotting (32). The results revealed that the expression of KIM-1 in the kidney of WT + HFD + STZ mice was clearly raised compared with WT mice (Fig. 1C and D; P<0.01), but was markedly reduced in Trpc6^−/− + HFD + STZ mice compared with WT + HFD + STZ mice (Fig. 1C and D; P<0.01). PAS staining was used to assess glomerulosclerosis and renal damage (33). The PAS staining results revealed that more PAS-positive substances were found in the glomeruli and renal tubulointerstitial in WT + HFD + STZ mice compared with the WT mice (Fig. 2A-C; P<0.01). Trpc6 knockout significantly alleviated PAS-positive substances in Trpc6^−/− + HFD + STZ mice compared with WT + HFD + STZ mice (Fig. 2A-C; P<0.05). The results revealed that Trpc6 knockout clearly protected against renal injury in T2DM mice.

Renal fibrosis is another important marker of renal damages. The present study used Masson staining to examine whether Trpc6 knockout had protective effects on glomerular fibrosis in T2DM mice. The results indicated that little fibrosis was found in the renal tubules and glomeruli in the WT, Trpc6^−/− and Trpc6^−/− + HFD groups. Compared with the WT mice, the tubular interstitial and glomerular fibrosis (blue) was markedly increased in WT + HFD + STZ mice (Fig. 2A and D; P<0.01). By contrast, Trpc6 knockout clearly alleviated renal fibrosis in Trpc6^−/− + HFD + STZ mice compared with WT + HFD + STZ mice (Fig. 2A and D; P<0.05). The results revealed that knockout Trpc6 may protect against renal fibrosis in T2DM mice and that HFD treatment alone had no influence on renal injury in Trpc6^−/− mice.

Transmission electron microscopy was performed to detect the effect of Trpc6 knockout on the glomerular microstructure in T2DM mice. The results showed that there was almost no glomerular damage in WT, Trpc6^−/− and Trpc6^−/− + HFD group non-T2DM mice (Fig. 3). Compared with the WT control mice, the WT + HFD + STZ mice showed obvious glomerular ultrastructure damages. The foot processes showed obvious fusion and disappearance (Fig. 3). However, Trpc6 knockout clearly improved these glomerular ultrastructure damages in Trpc6^−/− + HFD + STZ mice when compared with WT + HFD + STZ mice (Fig. 3). The data indicate that Trpc6 knockout clearly improves the glomerular ultrastructure in T2DM mice.

ROS-induced oxidative stress injury plays a main role in DKD progression (34); therefore, ROS accumulation in the renal cortex was assessed using DHE staining. The results revealed that there was almost no ROS production in the renal cortex in the WT and Trpc6^−/− mice. Compared with the WT mice, ROS production was clearly increased in both WT + HFD + STZ mice and Trpc6^−/− + HFD + STZ mice (Fig. 4A and B; P<0.01). Similarly, ROS production was also slightly raised in Trpc6^−/− + HFD mice (Fig. 4A and B; P<0.01). These data indicated that knockout Trpc6 showed no influence on the production of ROS in the renal cortex of T2DM mice and that ROS may be an upstream regulator of TRPC6 in T2DM.

β-Gal is one of the essential markers of cellular senescence and is also involved in the pathogenesis of renal fibrosis (35). The present study developed a β-Gal staining to assess renal senescence in T2DM mice. The results revealed that there was only a small amount of β-Gal expression in the WT and Trpc6^−/− groups. Compared with WT mice, the expression of β-Gal was clearly increased in WT + HFD + STZ mice (Fig. S3A and B; P<0.01). The activities of β-Gal were also increased in Trpc6^−/− + HFD mice when compared with Trpc6^−/− mice (Fig. S3A and B; P<0.01). However, the activities of β-Gal were clearly reduced in Trpc6^−/− + HFD + STZ mice when compared with WT + HFD + STZ mice (Fig. S3A and B; P<0.01). These results indicated that knockout of Trpc6 improved renal aging injury in T2DM mice.

To confirm the role of Trpc6 knockout in renal fibrosis in T2DM mice, the expression of the COL4 and FN genes were measured using immunohistochemistry (36). The results demonstrated that the expression of COL4 and FN were clearly increased in the kidney of WT + HFD + STZ mice when compared with WT mice (Fig. 5A-C; P<0.01) and the expression of COL4 and FN were clearly reduced in the Trpc6^−/− + HFD + STZ mice compared with WT + HFD + STZ mice (Fig. 5A-C; P<0.05 or P<0.01). The results indicated that knockout Trpc6 can alleviate renal fibrosis in T2DM-induced DKD.

In addition, the levels of TGF-β and p-SMAD2/3 proteins were examined in T2DM mice. The results showed that the levels of TGF-β and p-SMAD2/3 were clearly raised in WT + HFD + STZ mice when compared with WT control mice (Fig. 6A, B and D; P<0.01); however, the expression of p-SMAD2/3 and TGF-β were clearly decreased in the Trpc6^−/− + HFD + STZ mice when compared with WT + HFD + STZ mice (Fig. 6A, B and D; P<0.05). The results indicated that knockout of Trpc6 may attenuate renal fibrosis by inhibiting the pathway of TGF-β/SMAD2/3in T2DM mice.

Next, NLRP3 inflammasomes in the kidney were measured to investigate whether Trpc6 knockout can attenuate renal inflammation in T2DM mice. The results revealed that expression of NLRP3, cleaved-caspase-1 (P20) and ASC were clearly raised in the renal cortex of WT + HFD + STZ mice when compared with WT mice (Fig. 7A-D; P<0.01). However, Trpc6 knockout clearly decreased the expression of NLRP3, caspase-1 and ASC in Trpc6^−/− + HFD + STZ mice when compared with WT + HFD + STZ mice (Fig. 7A-D; P<0.01 or P<0.05). The results suggested that T2DM promoted renal inflammation and that Trpc6 knockout attenuated renal inflammation by inhibiting NLRP3 inflammasomes in T2DM.

The effect of Trpc6 knockout on CD36 and p-PLC expression in T2DM mice was evaluated. The results revealed that CD36 and p-PLC expression was markedly upregulated in the kidney of WT + HFD + STZ mice and Trpc6^−/− + HFD + STZ mice when compared with WT control mice (Fig. S4A-D; P<0.01 or P<0.05). Compared with the WT + HFD + STZ mice, knockout Trpc6 had no significant influence on the levels of CD36 and p-PLC/PLC in renal cortex tissues of T2DM mice (Fig. S4A-D; P>0.05). The results suggest that the CD36 and PLC signaling may be the upstream regulator of TRPC6 in T2DM mice.

Nile red staining was used to assess the amount of lipid deposition in kidney. The results revealed that the renal lipid deposition in WT + HFD + STZ mice and Trpc6^−/− + HFD + STZ groups was markedly increased when compared with WT control mice (Fig. S5A and B; P<0.01) and that knockout Trpc6 shows no significant influence on renal lipid deposition in T2DM mice. Similarly, HFD-treatment alone also increased renal lipid deposition in Trpc6^−/− + HFD mice (Fig. S5A and B; P<0.01). These data indicated that knockout Trpc6 has no significant effect on the renal lipid deposition in T2DM mice and that lipid deposition may be the upstream regulator of TRPC6 in T2DM.

Next, changes in CN-NFAT2 signaling in Trpc6^−/− T2DM was detected mice. The results revealed that there was a slight expression of TRPC6 in the kidney cortex of WT mice, but that TRPC6 expression was markedly increased in the kidneys of WT + HFD + STZ mice when compared with WT control mice (Fig. 8A and B; P<0.01). Additionally, TRPC6 was almost absent in kidney tissues of Trpc6^−/− mice, Trpc6^−/− + HFD mice and Trpc6^−/− + HFD + STZ mice. Furthermore, the results indicated that CN and NFAT2 expression was markedly increased in the kidneys of WT + HFD + STZ mice when compared with WT control mice (Fig. 8A and B; P<0.01); however, Trpc6 knockout clearly decreased CN and NFAT2 expression in the kidney of Trpc6^−/− + HFD + STZ mice when compared with WT + HFD + STZ mice (Fig. 8A and B; P<0.05). The results indicated that TRPC6-CN-NFAT2 signaling may play a key role in promoting DKD in T2DM and that Trpc6 knockout can partially inhibit the CN-NFAT2 signaling pathway in mice of T2DM.

Finally, the effects of Trpc6 knockdown on [Ca²⁺]_i was evaluated by using calcium imaging in PA + HG-induced HMCs. The results revealed that the HMCs exhibited a significant calcium overload after PA + HG stimulation with [Ca²⁺]_i increase and calcium homeostasis imbalance after BAPTA and CaCl₂ stimulation, compared with the control group (Fig. 9A-D; P<0.01 or P<0.05). As compared with the PA + HG group, treatment with TRPC6-siRNA decreased the [Ca²⁺]_i and reduced the Δ Ratio F340/F380 induced by BAPTA and CaCl₂ stimulation (Fig. 9A-D; P<0.01 or P<0.05). These results indicated that PA + HG treatment can activate the TRPC6 channels in HMCs and that Trpc6 knockdown can ameliorate the dysregulation of calcium homeostasis induced by PA + HG.