TRP Proteins Research Articles

P0651 Evaluating tryptophan as a biomarker for treatment success in Inflammatory Bowel Disease patients undergoing therapy

Abstract Background Patients with inflammatory bowel disease (IBD) display heterogenous responses to different treatment modalities suggesting distinct disease pathomechanisms. Herein, tryptophan (Trp) metabolism is associated with a range of chronic inflammatory disease, but the relevance to guide treatment decision in IBD remains unclear. Here, we sought to evaluate Trp serum level as a biomarker of treatment response in IBD in comparison to established disease biomarkers. Methods We analyzed and compared the serum levels of Trp and C-reactive protein (CRP) from patients with Ulcerative Colitis (UC) (n = 15) and Crohns Disease (CD) (n = 10). Longitudinal analyses of 100 serum Trp measurements were obtained and associated with inflammatory IBD markers during the induction period of various biological agents including TNF-α inhibitors (n=2), interleukin inhibitors (n=11), JAK inhibitors (n= 8), Sphingosine modulators (n=3) and integrin inhibitors (n=1). Results As expected, we found an inverse correlation between CRP and Trp (rs = -0.219, p = 0.045), indication a weak, negative correlation between the two variables across all patients. However, while this effect was predominantly observed in UC (r = - 0.317, p = 0.003), patients with CD showed no significant correlation between CRP and Trp levels (rs = -0.082, p = 0.763). In line with these findings, the observed correlation showed significant correlation in the different treatment modalities. Patients who received either interleukin- or JAK inhibitors displayed a stronger correlation (rs = -0.542, p = 0.001 and rs = - 0.358, p = 0.007 respectively), while patients receiving TNF-α-/ integrin inhibitors or Sphingosine-1-phosphate receptor modulators did not show a significant correlation. Conclusion Highlighting the heterogeneity of responses to different biologics, we observed a correlation between high serum Trp levels and a decline in biomarkers associated with a disease flare. These observations were most pronounced in patients with UC receiving treatment with interleukin- and JAK inhibitors suggesting potential therapeutic relevance in indicating early signs of successful induction treatment. References Wang S, van Schooten FJ, Jin H, Jonkers D, Godschalk R. The Involvement of Intestinal Tryptophan Metabolism in Inflammatory Bowel Disease Identified by a Meta-Analysis of the Transcriptome and a Systematic Review of the Metabolome. Nutrients. 2023 Jun 26;15(13):2886. doi: 10.3390/nu15132886. PMID: 37447212; PMCID: PMC10346271. Ding, Xueyan, Bin, Peng, Wu, Wenwen, Chang, Yajie, Zhu, Guoqiang, Tryptophan Metabolism, Regulatory T Cells, and Inflammatory Bowel Disease: A Mini Review, Mediators of Inflammation, 2020, 9706140, 10 pages, 2020. https://doi.org/10.1155/2020/9706140 Susanna Nikolaus, Berenice Schulte, Natalie Al-Massad, Florian Thieme, Dominik M. Schulte, Johannes Bethge, Ateequr Rehman, Florian Tran, Konrad Aden, Robert Häsler, Natalie Moll, Gregor Schütze, Markus J. Schwarz, Georg H. Waetzig, Philip Rosenstiel, Michael Krawczak, Silke Szymczak, Stefan Schreiber,Increased Tryptophan Metabolism Is Associated With Activity of Inflammatory Bowel Diseases,Gastroenterology,Volume 153, Issue 6,2017,Pages 1504-1516.e2,ISSN 0016-5085,https://doi.org/10.1053/j.gastro.2017.08.028.

Mechanistic Insights into the Stimulatory Effect of Melanogenesis of 4-Methylcoumarin Derivatives in B16F10 Melanoma Cells.

Vitiligo is a skin condition characterized by the loss of pigment, resulting in white patches on various parts of the body. It occurs when melanocytes, the cells that are responsible for producing skin pigment, are destroyed or stop functioning. This study aimed to investigate the melanogenic potential of various 4-methylcoumarin (4MC) derivatives, including 6-methoxy-4-methylcoumarin (6M-4MC), 7-methoxy-4-methylcoumarin (7M-4MC), 7-amino-4-methylcoumarin (7A-4MC), 6,7-dihydroxy-4-methylcoumarin (6,7DH-4MC), 7,8-dihydroxy-4-methylcoumarin (7,8DH-4MC), and 6,7-dimethoxy-4-methylcoumarin (6,7DM-4MC), in B16F10 melanoma cells. Our findings revealed that, while 4MC, 7A-4MC, 6,7DH-4MC, and 7,8DH-4MC did not exhibit any effect on melanin production, significant stimulation of melanogenesis was observed with 6M-4MC, 7M-4MC, and 6,7DM-4MC, with 6M-4MC demonstrating the most pronounced effect. 6M-4MC significantly stimulated melanin production and tyrosinase activity in a concentration-dependent manner in B16F10 cells. A Western blot analysis revealed that 6M-4MC increased the expression levels of microphthalmia-associated transcription factor (MITF), tyrosinase, tyrosinase-related protein-1 (TRP-1), and tyrosinase-related protein-2 (TRP-2). Further mechanistic studies showed that 6M-4MC inhibited extracellular signal-regulated kinase (ERK) and protein kinase B (AKT), which led to the upregulation of MITF and TRP proteins and subsequent activation of melanin synthesis. Additionally, 6M-4MC activated GSK3β phosphorylation, reduced β-catenin phosphorylation, and stimulated melanogenesis via the GSK3β/β-catenin pathway. Moreover, a primary skin irritation test was conducted on the upper backs of 32 healthy female volunteers to assess the potential irritation or sensitization from 6M-4MC when applied topically at concentrations of 50 µM and 100 µM. The test results showed no adverse effects on the skin. Collectively, these findings suggest that 6M-4MC may be a promising pigmentation stimulator for use in cosmetics and in the medical treatment of hypopigmentation disorders, particularly in the treatment of skin conditions such as vitiligo.

TRPV4-A Multifunctional Cellular Sensor Protein with Therapeutic Potential.

Transient receptor potential vanilloid (TRPV) channel proteins belong to the superfamily of TRP proteins that form cationic channels in the animal cell membranes. These proteins have various subtype-specific functions, serving, for example, as sensors for pain, pressure, pH, and mechanical extracellular stimuli. The sensing of extracellular cues by TRPV4 triggers Ca2+-influx through the channel, subsequently coordinating numerous intracellular signaling cascades in a spatio-temporal manner. As TRPV channels play such a wide role in various cellular and physiological functions, loss or impaired TRPV protein activity naturally contributes to many pathophysiological processes. This review concentrates on the known functions of TRPV4 sensor proteins and their potential as a therapeutic target.

Ligustilide covalently binds to Cys703 in the pre-S1 helix of TRPA1, blocking the opening of channel and relieving pain in rats with acute soft tissue injury

Ethnopharmacological relevanceThe natural anodyne Ligustilide (Lig), derived from Angelica sinensis (Oliv.) Diels and Ligusticum chuanxiong Hort., has been traditionally employed for its analgesic properties in the treatment of dysmenorrhea and migraine, and rheumatoid arthritis pain. Despite the existing reports on the correlation between TRP channels and the analgesic effects of Lig, a comprehensive understanding of their underlying mechanisms of action remains elusive. Aim of the studyThe objective of this study is to elucidate the mechanism of action of Lig on the analgesic target TRPA1 channel. MethodsThe therapeutic effect of Lig was evaluated in a rat acute soft tissue injury model. The analgesic target was identified through competitive inhibition of TRP channel agonists at the animal level, followed by Fluo-4/Ca2+ imaging on live cells overexpressing TRP proteins. The potential target was verified through in-gel imaging, colocalization using a Lig-derived molecular probe, and a drug affinity response target stability assay. The binding site of Lig was identified through protein spectrometry and further analyzed using molecular docking, site-specific mutation, and multidisciplinary approaches. ResultsThe administration of Lig effectively ameliorated pain and attenuated oxidative stress and inflammatory responses in rats with soft tissue injuries. Moreover, the analgesic effects of Lig were specifically attributed to TRPA1. Mechanistic studies have revealed that Lig directly activates TRPA1 by interacting with the linker domain in the pre-S1 region of TRPA1. Through metabolic transformation, 6,7-epoxyligustilide (EM-Lig) forms a covalent bond with Cys703 of TRPA1 at high concentrations and prolonged exposure time. This irreversible binding prevents endogenous electrophilic products from entering the cysteine active center of ligand-binding pocket of TRPA1, thereby inhibiting Ca2+ influx through the channel opening and ultimately relieving pain. ConclusionsLig selectively modulates the TRPA1 channel in a bimodal manner via non-electrophilic/electrophilic metabolic conversion. The epoxidized metabolic intermediate EM-Lig exerts analgesic effects by irreversibly inhibiting the activation of TRPA1 on sensory neurons. These findings not only highlight the analgesic mechanism of Lig but also offer a novel nucleophilic attack site for the development of TRPA1 antagonists in the pre-S1 region.

Tryptophan degradation as a systems phenomenon in inflammation – an analysis across 13 chronic inflammatory diseases

Chronic inflammatory diseases (CIDs) are systems disorders that affect diverse organs including the intestine, joints and skin. The essential amino acid tryptophan (Trp) can be broken down to various bioactive derivatives important for immune regulation. Increased Trp catabolism has been observed in some CIDs, so we aimed to characterise the specificity and extent of Trp degradation as a systems phenomenon across CIDs. We used high performance liquid chromatography and targeted mass spectrometry to assess the serum and stool levels of Trp and Trp derivatives. Our retrospective study incorporates both cross-sectional and longitudinal components, as we have included a healthy population as a reference and there are also multiple observations per patient over time. We found reduced serum Trp levels across the majority of CIDs, and a prevailing negative relationship between Trp and systemic inflammatory marker C-reactive protein (CRP). Notably, serum Trp was low in several CIDs even in the absence of measurable systemic inflammation. Increases in the kynurenine-to-Trp ratio (Kyn:Trp) suggest that these changes result from increased degradation along the kynurenine pathway. Increases in Kyn:Trp indicate the kynurenine pathway as a major route for CID-related Trp metabolism disruption and the specificity of the network changes indicates excessive Trp degradation relative to other proteogenic amino acids. Our results suggest that increased Trp catabolism is a common metabolic occurrence in CIDs that may directly affect systemic immunity. This work was supported by the DFG Cluster of Excellence 2167 "Precision medicine in chronic inflammation" (KA, SSchr, PR, BH, SWa), the BMBF (e:Med Juniorverbund "Try-IBD" 01ZX1915A and 01ZX2215, the e:Med Network iTREAT 01ZX2202A, and GUIDE-IBD 031L0188A), EKFS (2020_EKCS.11, KA), DFG RU5042 (PR, KA), and Innovative Medicines Initiative 2 Joint Undertakings ("Taxonomy, Treatments, Targets and Remission", 831434, "ImmUniverse", 853995, "BIOMAP", 821511).

Transient receptor potential channel 3 in human liver and gallbladder – An investigation in body donors

Since the discovery of TRP proteins in 1969, during studies of the fruit fly Drosophila melanogaster, interest around them and the subfamily of TRPC channels has remained high. TRPC3 was able to be detected in a number of organs in rodents, such as rats and mice, and also in various human tissues. For the most part, these investigations were carried out using gene expression of TRPC3. Further work has already confirmed the relevance of TRPC3 in the context of neurodegenerative diseases, such as spinocerebellar ataxia, and carcinogenic entities, such as ovarian carcinoma. An association with TRPC3 has also been demonstrated for diseases that affect the liver. In order to confirm the expression of TRPC3 in the human liver, this study uses samples taken from eight (n = 8) fixated human body donors and analyzed with immunohistochemistry. In accordance with the macroscopic anatomy of the organs, six samples (n = 6) of liver tissue and three (n = 3) of gallbladder tissue were obtained. TRPC3 was clearly detected in all liver and gallbladder samples examined. Thus, it is not unlikely that TRPC3 plays a role in the extensive metabolic processes of the liver and could also serve as a target for pharmacological interventions in an imbalance of calcium homeostasis.

Detection of TRPM6 and TRPM7 Proteins in Normal and Diseased Cardiac Atrial Tissue and Isolated Cardiomyocytes

Magnesium-sensitive transient receptor potential melastatin (TRPM) ion channels, TRPM6 and TRPM7, are present in several organs, but their roles in the heart remain unclear. Therefore, here, we studied the expression patterns of TRPM6 and TRPM7 in normal and diseased myocardium. Cardiac atrial tissue and cardiomyocytes were obtained from healthy pigs and undiseased human hearts as well as from hearts of patients with ischemic heart disease (IHD) or atrial fibrillation (AF). Immunofluorescence and ELISA were used to detect TRP proteins. TRPM6 and TRPM7 immunofluorescence signals, localized at/near the cell surface or intracellularly, were detected in pig and human atrial tissues. The TRP channel modulators carvacrol (CAR, 100 µM) or 2-aminoethoxydiphenyl borate (2-APB, 500 µM) decreased the TRPM7 signal, but enhanced that of TRPM6. At a higher concentration (2 mM), 2-APB enhanced the signals of both proteins. TRPM6 and TRPM7 immunofluorescence signals and protein concentrations were increased in atrial cells and tissues from IHD or AF patients. TRPM6 and TRPM7 proteins were both detected in cardiac atrial tissue, with relatively similar subcellular localization, but distinctive drug sensitivity profiles. Their upregulated expression in IHD and AF suggests a possible role of the channels in cardiac atrial disease.

Systematic Analysis and Identification of Molecular Subtypes of TRP-Related Genes and Prognosis Prediction in Lung Adenocarcinoma.

Background Transient receptor potential channel (TRP) is a superfamily of nonselective cation channels, which is a member of calcium ion channels with a vital role in different calcium ion signal transduction pathways. TRP channel expression is often changed in the tumor, although the role of TRP proteins in lung cancer is unknown. Methods Molecular Signatures Database (MsigDB) provided the TRP gene set. Univariate Cox regression analysis was performed on The Cancer Genome Atlas Lung Adenocarcinoma (TCGA-LUAD) data collection set employing the coxph function of R package survival to find prognosis-related genes. The R package ConsumusClusterPlus was employed for doing the consistency cluster analysis of TCGA-LUAD samples according to the prognosis-related TRP gene. The R-package limma was utilized for investigating the differential expression of TRP subtypes. According to the differentially expressed genes between subtypes, the least absolute shrinkage and selection operator (LASSO) regression was employed to find the major genes and develop the risk model. CIBERPORT algorithm, R package maftools, gene set variation analysis (GSVA), and pRRophetic of R-package were employed for measuring the proportion of immune cells among subtypes, genomic mutation difference, pathway enrichment score, and drug sensitivity analysis. Results A total of 15 TRP-related genes associated with the prognosis of lung adenocarcinoma were found. According to the expression value of 15 genes, lung adenocarcinoma can be sorted into two subcategories. The prognosis of cluster1 is considerably better in comparison with that of cluster2. There were 123 differentially expressed genes between C1 and C2 subtypes, including 6 up- and 117 downregulated genes. There were major variations in the tumor microenvironment between C1 and C2 subtypes. The proportion of CD8 T cells in the C1 subtype was considerably enhanced in comparison with that in the C2 subtype. We further discovered 123 differentially expressed genes among subtypes, and 8 key genes were obtained at the end. The risk score (RS) model developed by the 8-gene signature had good strength in the TCGA validation set, overall set, and Gene Expression Omnibus (GEO) external dataset. There were major variations in immune checkpoint gene expression, patient sensitivity to immunotherapeutic drugs, immune infiltration, and genomic mutations between high and low groups on the basis of RS. Conclusions The risk model developed on the basis of TRP-related genes can help in predicting the prognosis of patients suffering from lung adenocarcinoma and guide immunotherapy.

PSV-7 Effects of Feed Additives Ambitine and Taktik X-Hit on Amino Acid Digestibility in Pigs

Abstract Improvements in digestion of amino acids (AA) in the small intestine of pigs improve feed efficiency and feed conversion. Non-nutritive feed additives that improve growth performance may affect AA digestibility. Therefore, the objective of the study was to investigate 2 different feed additives in the diets of grower pigs on ileal digestibility of AA. A total of 10 pigs, 5 barrows and 5 gilts, were surgical implanted with ileal cannulas. Each pig was randomly assigned to 1 of 3 dietary treatments, in 3 different collection periods, according to a Latin Square design. Dietary treatments were as follows: 1) Control – standard corn soybean-meal diet; 2) Control plus the addition of Ambitine at 1 kg/tonne; 3) Control plus the addition of TakTik X-Hit at 100 grams/tonne. An indigestible marker of 0.3% titanium was included in each dietary treatment. Each pig was fed the assigned dietary treatment ration at 4% of body weight. Following an adaption of 5 d, ileal digesta was then collected over a 2-d period for 12 hours each collection day. Diets and digesta were analyzed for AA concentrations to determine AA digestibility and basal endogenous losses were measured by feeding a nitrogen free diet. There were no differences (P >0.05) in AID or SID of AA Lys (92%), Thr (89%), Trp (91%), Met (94%) or crude protein (89%) according to feed additive inclusions. These results indicate that the inclusion of the non-nutritive feed additives Ambitine and TakTik X-Hit did not impact AA digestibility.

INFLUENCE OF pH ON THE SPECTRAL-LUMINESCENT CHARACTERISTICS OF THE SOFT PROTEIN CROWN OF SILVER NANOPARTICLES

The spectral and fluorescent characteristics of bovine serum albumin (BSA) molecules in the soft crown of silver nanoparticles (AgNP) were studied at different pH values. The formation of BSA + AgNP complexes was established. The coupling constants of the complex (Kass) and the biomolecular rate constants of the BSA fluorescence quenching (Kq) were determined for different pH values. The dependences of Kass and Kq on pH are nonmonotonic with maxima at pH 6.0. The number of binding sites (Hill coefficient (n)) and the thickness of the BSA soft crown (d) are also maximal at pH 6.0. At higher and lower pH values (relative
 to pH 6.0), these parameters decrease. Variations in the parameters of interaction between BSA and AgNP are due to changes in the conformational modifications of the protein (content of the а-helix) and the microenvironment of Tyr and Trp protein residues in the soft crown (hydrophobicity of the protein).

Optimization and characterization of electrochemical protein Imprinting on hemispherical porous gold patterns for the detection of trypsin

In this study, protein-imprinted sensors with thin bulk films were electrochemically fabricated on gold-coated quartz crystal electrodes with hemispherical porous gold patterns for detecting trypsin (Trp). The gold patterns were electrodeposited on a polystyrene colloidal monolayer and then rinsed using toluene. For Trp imprinting on the gold patterned electrodes, a thin layer with a poly(o-phenylenediamine) and Trp protein was formed using a cyclic voltammetry method under optimized conditions. In addition, a two-dimensional molecularly imprinted polymer (2D-MIP) film was prepared on a planar gold electrode under the same conditions to compare to the dependence of Trp selective recognition on three-dimensional (3D) thin MIP structure, and each corresponding nonimprinted polymer film were constructed by electropolymerization, in the absence of Trp template, to compare molecular imprinting effects. The sensing properties of Trp imprinted sensors were investigated using electrochemical, such as cyclic voltammetry and electrochemical impedance spectroscopy, and microgravimetric methods to confirm the sensitivity and selectivity of MIP films. The 3D-MIP films demonstrated a higher imprinting factor (3.51) in 48-μg/mL of Trp concentration than the 2D-MIP film, and the limit of detection was calculated to be 70.9-ng/mL. In addition, the films exhibited higher electrochemical sensing responses due to increased Trp recognition by the effective molecular imprinting over a larger surface area. Thus, the construction of 3D-MIP films for the protein imprinting could provide excellent specificity, faster kinetics, and higher sensitivity for detecting macromolecular proteins than 2D-MIP films.

ASIC1a is required for neuronal activation via low-intensity ultrasound stimulation in mouse brain.

Accumulating evidence has shown transcranial low-intensity ultrasound can be potentially a non-invasive neural modulation tool to treat brain diseases. However, the underlying mechanism remains elusive and the majority of studies on animal models applying rather high-intensity ultrasound that cannot be safely used in humans. Here, we showed low-intensity ultrasound was able to activate neurons in the mouse brain and repeated ultrasound stimulation resulted in adult neurogenesis in specific brain regions. In vitro calcium imaging studies showed that a specific ultrasound stimulation mode, which combined with both ultrasound-induced pressure and acoustic streaming mechanotransduction, is required to activate cultured cortical neurons. ASIC1a and cytoskeletal proteins were involved in the low-intensity ultrasound-mediated mechanotransduction and cultured neuron activation, which was inhibited by ASIC1a blockade and cytoskeleton-modified agents. In contrast, the inhibition of mechanical-sensitive channels involved in bilayer-model mechanotransduction like Piezo or TRP proteins did not repress the ultrasound-mediated neuronal activation as efficiently. The ASIC1a-mediated ultrasound effects in mouse brain such as immediate response of ERK phosphorylation and DCX marked neurogenesis were statistically significantly compromised by ASIC1a gene deletion. Collated data suggest that ASIC1a is the molecular determinant involved in the mechano-signaling of low-intensity ultrasound that modulates neural activation in mouse brain.

TRPV Protein Family-From Mechanosensing to Cancer Invasion.

Biophysical cues from the cellular microenvironment are detected by mechanosensitive machineries that translate physical signals into biochemical signaling cascades. At the crossroads of extracellular space and cell interior are located several ion channel families, including TRP family proteins, that are triggered by mechanical stimuli and drive intracellular signaling pathways through spatio-temporally controlled Ca2+-influx. Mechanosensitive Ca2+-channels, therefore, act as critical components in the rapid transmission of physical signals into biologically compatible information to impact crucial processes during development, morphogenesis and regeneration. Given the mechanosensitive nature of many of the TRP family channels, they must also respond to the biophysical changes along the development of several pathophysiological conditions and have also been linked to cancer progression. In this review, we will focus on the TRPV, vanilloid family of TRP proteins, and their connection to cancer progression through their mechanosensitive nature.

Modeling the Menthol Binding Pocket Within TRPM8 Ion Channel

Menthol is a natural substance that induces a cooling sensation. It is common in remedies used to soothe aching muscles. The menthol receptor, TRP melastatin 8 (TRPM8), is one of eight members of the TRP protein superfamily and is activated by physical stimuli such as cold and chemical stimuli such as the ligand menthol. The menthol binding takes place within the putative menthol-binding pocket, located within the transmembrane domain of TRPM8 channel, however, due to a lack of TRPM8 structure with menthol bound, the binding configuration of menthol is unknown. The Summit Country Day School MSOE Center for Biomolecular Modeling MAPS Team used 3D modeling and printing technology to examine the structure-function relationship of the menthol binding pocket on TRPM8. The menthol-binding pocket can be found within the transmembrane domain of the TRPM8 channel near Y745 and R842 within the S1–S4 domain. Computational and functional analysis have suggested that menthol uses its hydroxyl group “hand” to grab the R842 side chain, and its isopropyl group “legs” to stand on I846 and L843. Menthol's hydroxyl group binds with R842 likely through a hydrogen bond, while its isopropyl legs stand on residues on S4 through Van Der Waal Interactions. This binding causes a conformational rearrangement of the binding pocket of of amino acids Y745, R842 and D802, allowing ions to pass through the channel. TRPM8 may be involved in many pathological processes such as cold hyperplasia, irritable bowel disease, prostate cancer, and migraines. Therefore, understanding the binding site of menthol in the TRPM8 channel may be important not only for designing potential drug targets but also the mechanism of regulating TRPM8 activity.

Thermo-mechanical pain: the signaling role of heat dissipation in biological tissues

Mechanical algesia is an important process for the preservation of living organisms, allowing potentially life-saving reflexes or decisions when given body parts are stressed. Yet, its various underlying mechanisms remain to be fully unraveled. Here, we quantitatively discuss how the detection of painful mechanical stimuli by the human central nervous system may, partly, rely on thermal measurements. Indeed, most fractures in a body, including microscopic ones, release some heat, which diffuses in the surrounding tissues. Through this physical process, the thermo-sensitive TRP proteins, that translate abnormal temperatures into action potentials, shall be sensitive to damaging mechanical inputs. The implication of these polymodal receptors in mechanical algesia has been regularly reported, and we here provide a physical explanation for the coupling between thermal and mechanical pain. In particular, in the human skin, we show how the neighboring neurites of a broken collagen fiber can undergo a sudden thermal elevation that ranges from a fraction to tens of degrees. As this theoretical temperature anomaly lies in the sensibility range of the TRPV3 and TRPV1 cation channels, known to trigger action potentials in the neural system, a degree of mechanical pain can hence be generated.

Inherited Cardiac Arrhythmia Syndromes: Focus on Molecular Mechanisms Underlying TRPM4 Channelopathies.

The Transient Receptor Potential Melastatin 4 (TRPM4) is a transmembrane N-glycosylated ion channel that belongs to the large family of TRP proteins. It has an equal permeability to Na+ and K+ and is activated via an increase of the intracellular calcium concentration and membrane depolarization. Due to its wide distribution, TRPM4 dysfunction has been linked with several pathophysiological processes, including inherited cardiac arrhythmias. Many pathogenic variants of the TRPM4 gene have been identified in patients with different forms of cardiac disorders such as conduction defects, Brugada syndrome, and congenital long QT syndrome. At the cellular level, these variants induce either gain- or loss-of-function of TRPM4 channels for similar clinical phenotypes. However, the molecular mechanisms associating these functional alterations to the clinical phenotypes remain poorly understood. The main objective of this article is to review the major cardiac TRPM4 channelopathies and recent advances regarding their genetic background and the underlying molecular mechanisms.

Pressure‐Induced Constriction of the Middle Cerebral Artery is Abolished in TrpC6 Knockout Mice

Pressure‐induced constriction (PIC) is an inherent response of small arteries and arterioles in which increases in intraluminal pressure evoke vasoconstriction. It is a critical mechanism of blood flow autoregulation in the kidney and brain. Degenerin (Deg) and transient receptor potential (Trp) protein families have been implicated in transduction of PIC because of evolutionary links to mechanosensing in the nematode and fly. We hypothesize that Deg and Trp proteins associate to form a multi‐meric mechanosensing complex in vascular smooth muscle cells (VSMCs), in which Deg and Trp proteins play different, yet equally critical, roles as sensors and amplifiers, in PIC molecular signaling. Our laboratory has provided direct evidence that the Deg protein bENaC acts as a sensor by mediating mechanoreceptor currents in isolated VSMCs. While TrpC6 has been suggested to mediate PIC, direct supporting evidence is lacking. Therefore, the aim of this study was to determine the importance of TrpC6 in PIC signaling using a mouse model lacking TrpC6. To address this aim, we evaluated graded pressure (20–90 mm Hg), depolarization‐ (20–80 mM KCl) and adrenergic receptor‐(phenylephrine, PE 10−7–10−4 M) mediated constriction of isolated middle cerebral artery (MCA) segments from 9 weeks old male wild‐type (+/+, n=7) and homozygous null (−/−, n=9) TrpC6 mice (Jackson Laboratories). Isolated MCA segments were cannulated and pressurized with physiological salt solution using pressure myography (Living Systems). The data were analyzed preliminarily using independent 2‐tailed t‐test. Normalized MCA vasoconstrictor responses to KCl (80 mM, 45.5±1.1% vs 40.9±1.2%, p=0.2) and PE (10−4 M, 37.4±1.7% vs 38.7.0±1.2%, p=0.8) were similar in TrpC6−/− and TrpC6+/+ mice, respectively. In contrast, PIC responses were totally abolished in TrpC6 −/− mice; at 90 mmHg calculated myogenic tone was 0.8±0.5% vs 10.7±1.7%, p=0.0002, in TrpC6−/− and TrpC6+/+ mice, respectively. Additionally, there were no changes in mechanical properties of circumferential wall strain (0.2±0.02 vs. 0.2±0.02, p=0.8) and stress (2.7±0.1 vs. 3.1±0.4, p=0.4), at 90 mmHg; or morphological properties wall thickness (13.4±0.8μm vs. 14.3±1.5μm, p=0.6) and wall‐to‐lumen ratio (0.3±0.02 vs. 0.3±0.04, p=0.7), at 50 mmHg between TrpC6−/− and TrpC6+/+ mice. Although these results suggest that TrpC6 is required for the PIC response, they do not identify the role of TrpC6. Studies in the nematode suggest that Deg and Trp channels play different, yet equally critical roles in mechano‐signaling; Deg channels mediate mechanoreceptor currents, while Trp channels mediate post‐transduction signal amplification. Future studies will determine the role of TrpC6 in isolated VSMCs and cerebral blood flow autoregulation. This research was supported by P20GM104357, P20121334, P01HL051971, R01HL1136684.Support or Funding InformationP20GM104357, P20121334, P01HL051971, R01HL1136684.

The Role of TRPC1 in Modulating Cancer Progression.

Calcium ions (Ca2+) play an important role as second messengers in regulating a plethora of physiological and pathological processes, including the progression of cancer. Several selective and non-selective Ca2+-permeable ion channels are implicated in mediating Ca2+ signaling in cancer cells. In this review, we are focusing on TRPC1, a member of the TRP protein superfamily and a potential modulator of store-operated Ca2+ entry (SOCE) pathways. While TRPC1 is ubiquitously expressed in most tissues, its dysregulated activity may contribute to the hallmarks of various types of cancers, including breast cancer, pancreatic cancer, glioblastoma multiforme, lung cancer, hepatic cancer, multiple myeloma, and thyroid cancer. A range of pharmacological and genetic tools have been developed to address the functional role of TRPC1 in cancer. Interestingly, the unique role of TRPC1 has elevated this channel as a promising target for modulation both in terms of pharmacological inhibition leading to suppression of tumor growth and metastasis, as well as for agonistic strategies eliciting Ca2+ overload and cell death in aggressive metastatic tumor cells.

A novel pH sensor with application to milk based on electrochemical oxidative quinone-functionalization of tryptophan residues

The electrochemical oxidative quinone-functionalization of tryptophan (Trp) residues, and the proton-coupled electron transfer properties between quinonized Trp (Trp=O) and its re-reduced species (Trp-OH) are investigated for potentiometric pH sensors. The Trp=O/Trp-OH couples are assembled on a graphite electrode using multiple cyclic voltammetry, and exhibit a pair of well-defined redox peaks at redox potential of 0.090 V (vs. SCE) at pH 7.0 and 298 K. The proton-coupled electron transfer properties of Trp=O/Trp-OH couples are dependent on electrode substrate material, incubation temperature and pH values, and Trp residue sources including amino acid, peptide and protein. The Trp=O/Trp-OH-based surface-confined exothermic electrode reaction rates show a decrease with increasing incubation temperature from 283 to 323 K at pH 5.0. Both of redox peak potential and open-circuit potential under optimum conditions have a good linear pH dependence between 1.0 and 12.0 with sensitivity of more than 52 mV pH −1 and relative standard derivation of 1.5%. The proposed potentiometric pH sensor has significant advantages of low cost, good stability and reproducibility, and strong anti-interference ability. The present study shows a new approach to endow Trp, Trp-containing peptides and non-conjugated proteins with analogous proton-coupled electron transfer performance to prosthetic groups of quinoproteins for monitoring pH changes in milk samples.

Therapeutic Effect of Tetrapanax papyriferus and Hederagenin on Chronic Neuropathic Pain of Chronic Constriction Injury of Sciatic Nerve Rats Based on KEGG Pathway Prediction and Experimental Verification.

Background Hederagenin is one of the main components of Tetrapanax papyriferus, and Tetrapanax papyriferus is one of the ingredients of Danggui Sini decoction. To explore whether Tetrapanax papyriferus and hederagenin can alleviate mechanical pain, thermal hyperalgesia, and cold pain at the same time, we comprehensively investigated the effects of two drugs on the levels of p38 MAPK phosphorylation, TRP proteins, and IL1β, IL6, and TNF-α in serum. Methods Firstly, we obtained pain-related targets and performed KEGG pathway enrichment on these targets. Then, 42 SD rats were separated randomly into six groups: sham operation group, CCI group, pregabalin group, mecobalamin group, Tetrapanax papyriferus group, and hederagenin group. All drugs were given orally. Rats in the sham operation group and CCI group were gavaged with saline. Rats in the pregabalin group were given pregabalin, while rats in the mecobalamin group were given mecobalamin. Rats in the Tetrapanax papyriferus group were given Tetrapanax papyriferus, while rats in the hederagenin group were given hederagenin. Besides, we conducted behavioral tests including acetone test, hot plate experiment, and von Frey filaments, and then dorsal root ganglion neurons were taken out on the 21st day after operation. Then, western blot, ELISA, and hematoxylin-eosin staining were conducted. Results Rats in the CCI group were more sensitive to hyperalgesia and allodynia to mechanical and thermal stimuli, as well as cold pain. All four drugs could relieve these pains. Pregabalin, mecobalamin, and Tetrapanax papyriferus can reduce the levels of IL1β, IL6, and TNF-α in serum compared to those of the CCI group. The expression of TRPM8, TRPA1, TRPV1, TRPV4, and phosphorylated p38 MAPK in DRG increased evidently on the 21st day after the operation in the CCI group. All four drugs could reduce the expressions of TRPM8, TRPA1, TRPV1, TRPV4, and phosphorylated p38 MAPK in dorsal root ganglion compared to those of the CCI group. Conclusion Tetrapanax papyriferus and hederagenin relieved sciatica by reducing inflammation levels, inhibiting p38 MAPK phosphorylation, and decreasing the levels of dorsal root ganglion proteins.