Modulation of Hippo Pathway by Alternative Splicing Diwas Srivastava
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Dysfunctional Mechanotransduction Through the YAP/TAZ/Hippo Pathway As a Feature of Chronic Disease
cells Review Dysfunctional Mechanotransduction through the YAP/TAZ/Hippo Pathway as a Feature of Chronic Disease 1, 2, 2,3, 4 Mathias Cobbaut y, Simge Karagil y, Lucrezia Bruno y, Maria Del Carmen Diaz de la Loza , Francesca E Mackenzie 3, Michael Stolinski 2 and Ahmed Elbediwy 2,* 1 Protein Phosphorylation Lab, Francis Crick Institute, London NW1 1AT, UK; [email protected] 2 Department of Biomolecular Sciences, Kingston University, Kingston-upon-Thames KT1 2EE, UK; [email protected] (S.K.); [email protected] (L.B.); [email protected] (M.S.) 3 Department of Chemical and Pharmaceutical Sciences, Kingston University, Kingston-upon-Thames KT1 2EE, UK; [email protected] 4 Epithelial Biology Lab, Francis Crick Institute, London NW1 1AT, UK; [email protected] * Correspondence: [email protected] These authors contribute equally to this work. y Received: 30 November 2019; Accepted: 4 January 2020; Published: 8 January 2020 Abstract: In order to ascertain their external environment, cells and tissues have the capability to sense and process a variety of stresses, including stretching and compression forces. These mechanical forces, as experienced by cells and tissues, are then converted into biochemical signals within the cell, leading to a number of cellular mechanisms being activated, including proliferation, differentiation and migration. If the conversion of mechanical cues into biochemical signals is perturbed in any way, then this can be potentially implicated in chronic disease development and processes such as neurological disorders, cancer and obesity. This review will focus on how the interplay between mechanotransduction, cellular structure, metabolism and signalling cascades led by the Hippo-YAP/TAZ axis can lead to a number of chronic diseases and suggest how we can target various pathways in order to design therapeutic targets for these debilitating diseases and conditions. -
The Hippo Pathway Component Wwc2 Is a Key Regulator of Embryonic Development and Angiogenesis in Mice Anke Hermann1,Guangmingwu2, Pavel I
Hermann et al. Cell Death and Disease (2021) 12:117 https://doi.org/10.1038/s41419-021-03409-0 Cell Death & Disease ARTICLE Open Access The Hippo pathway component Wwc2 is a key regulator of embryonic development and angiogenesis in mice Anke Hermann1,GuangmingWu2, Pavel I. Nedvetsky1,ViktoriaC.Brücher3, Charlotte Egbring3, Jakob Bonse1, Verena Höffken1, Dirk Oliver Wennmann1, Matthias Marks4,MichaelP.Krahn 1,HansSchöler5,PeterHeiduschka3, Hermann Pavenstädt1 and Joachim Kremerskothen1 Abstract The WW-and-C2-domain-containing (WWC) protein family is involved in the regulation of cell differentiation, cell proliferation, and organ growth control. As upstream components of the Hippo signaling pathway, WWC proteins activate the Large tumor suppressor (LATS) kinase that in turn phosphorylates Yes-associated protein (YAP) and its paralog Transcriptional coactivator-with-PDZ-binding motif (TAZ) preventing their nuclear import and transcriptional activity. Inhibition of WWC expression leads to downregulation of the Hippo pathway, increased expression of YAP/ TAZ target genes and enhanced organ growth. In mice, a ubiquitous Wwc1 knockout (KO) induces a mild neurological phenotype with no impact on embryogenesis or organ growth. In contrast, we could show here that ubiquitous deletion of Wwc2 in mice leads to early embryonic lethality. Wwc2 KO embryos display growth retardation, a disturbed placenta development, impaired vascularization, and finally embryonic death. A whole-transcriptome analysis of embryos lacking Wwc2 revealed a massive deregulation of gene expression with impact on cell fate determination, 1234567890():,; 1234567890():,; 1234567890():,; 1234567890():,; cell metabolism, and angiogenesis. Consequently, a perinatal, endothelial-specific Wwc2 KO in mice led to disturbed vessel formation and vascular hypersprouting in the retina. -
Hippo Signaling Regulates Drosophila Intestine Stem Cell Proliferation Through Multiple Pathways
Hippo signaling regulates Drosophila intestine stem cell proliferation through multiple pathways Fangfang Rena, Bing Wanga, Tao Yuea, Eun-Young Yunb,1, Y. Tony Ipb, and Jin Jianga,c,2 aDepartment of Developmental Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390; bProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605; and cDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX 75390 Edited* by Michael Levine, University of California, Berkeley, CA, and approved October 6, 2010 (received for review August 27, 2010) Intestinal stem cells (ISCs) in the Drosophila adult midgut are essen- investigated. In this study, we demonstrate that the Hpo pathway tial for maintaining tissue homeostasis and replenishing lost cells in restricts ISC proliferation in the adult midgut. We uncover response to tissue damage. Here we demonstrate that the Hippo a non–cell-autonomous mechanism by which the Hpo pathway (Hpo) signaling pathway, an evolutionarily conserved pathway im- negatively regulates stem cell proliferation by restricting the plicated in organ size control and tumorigenesis, plays an essential production of cytokines and mitogens that activate the JAK- role in regulating ISC proliferation. Loss of Hpo signaling in either STAT and EGFR pathways. In addition, we demonstrate that midgut precursor cells or epithelial cells stimulates ISC proliferation. Yki is required in the precursor cells for dextran sulfate sodium We provide evidence that loss of Hpo signaling in epithelial cells (DSS)-induced ISC proliferation. increases the production of cytokines of the Upd family and multiple EGFR ligands that activate JAK-STAT and EGFR signaling pathways Results in ISCs to stimulate their proliferation, thus revealing a unique non– Loss of Hpo Signaling in Precursor Cells Stimulates ISC Proliferation. -
Hippo Signaling Pathway As a New Potential Target in Non-Melanoma Skin Cancers: a Narrative Review
life Review Hippo Signaling Pathway as a New Potential Target in Non-Melanoma Skin Cancers: A Narrative Review Igor Aleksander Bednarski 1,*, Magdalena Ci ˛azy˙ ´nska 2 , Karolina Wódz 3, Izabela Drózd˙ z˙ 4 , Małgorzata Skibi ´nska 1, Joanna Narbutt 1 and Aleksandra Lesiak 1 1 Department of Dermatology, Pediatric Dermatology and Dermatological Oncology, Medical University of Lodz, 91-347 Lodz, Poland; [email protected] (M.S.); [email protected] (J.N.); [email protected] (A.L.) 2 Department of Proliferative Diseases, Nicolaus Copernicus Multidisciplinary Centre for Oncology and Traumatology, 93-513 Lodz, Poland; [email protected] 3 Laboratory of Molecular Biology, VET-LAB Brudzew, 62-720 Brudzew, Poland; [email protected] 4 Department of Clinical Genetics, Medical University of Lodz, Pomorska 251, 92-213 Lodz, Poland; [email protected] * Correspondence: [email protected] Abstract: Non-melanoma skin cancers (NMSCs), including basal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (cSCC), are the most frequently diagnosed cancers in humans, however, their exact pathogenesis is not fully understood. In recent years, it has been hypothesized that the recently discovered Hippo pathway could play a detrimental role in cutaneous carcinogenesis, but no direct connections have been made. The Hippo pathway and its effector, YAP, are responsible for tissue growth by accelerating cell proliferation, however, YAP upregulation and overexpression have also been reported in numerous types of tumors. There is also evidence that disrupted YAP/Hippo Citation: Bednarski, I.A.; Ci ˛azy´nska,˙ signaling is responsible for cancer growth, invasion, and metastasis. -
Type I and II Interferon Are Associated with High Expression of the Hippo Pathway Family Members
Cel al & lul ic ar in I l m C m f o u n l a o l n o Journal of Clinical & Cellular r g u y o J ISSN: 2155-9899 Immunology Research Article Type I and II Interferon are Associated with High Expression of the Hippo Pathway Family Members Bianca Sciescia1*, Raquel Tognon2, Natalia de Souza Nunes1, Tathiane Maistro Malta1, Fabiani Gai Frantz1, Fabiola Attie de Castro1, Maira da Costa Cacemiro1 1Department of Clinical, Toxicological and Bromatological Analysis, University of Sao Paulo - USP, Ribeirao Preto - SP, Brazil; 2Department of Pharmacy, Federal University of Juiz de Fora, Campus Governador Valadares, Governador Valadares - MG, Brazil ABSTRACT The Hippo pathway plays a regulatory role on inflammation and cell death and proliferation. Here we described a relationship between Hippo pathway components and inflammation in healthy subjects. The plasma levels of cytokines and chemokines were used to define their inflammatory profile and classify them as normal, high and low producers of cytokines. Leukocytes from healthy subjects with inflammatory profile expressed the highest levels of MSTS1/MST2, SAV1, LATS1/LATS2, MOB1A/MOB1B and YAP genes. The group that overexpressed Hippo pathway-related genes secreted more IFN-ϒ and IFN-α2. Keywords: Hippo pathway; Inflammatory process; Healthy subjects; Cytokines; Chemokines ABBREVATIONS: LATS1/LATS2 kinases (large tumor suppressor kinase 1/2) and MOB kinase activator IL: Interleukin; IFN: Interferon; LATS1/LATS2: Large tumor their adapter proteins MOB1A/MOB1B ( 1A/1B yes-associated suppressor kinase 1/2; MCP-1: Monocyte chemoattractant ), and the transcription coactivators YAP ( protein tafazzin protein protein-1; MIP: Macrophage inflammatory protein; MOB1A/ ) and TAZ ( ). -
Hippo Signaling Antibody Sampler
Hippo Signaling Antibody Sampler Kit Store at -20°C 3 n 1 Kit Orders n 877-616-CELL (2355) (9 x 20 µl) [email protected] Support n 877-678-TECH (8324) [email protected] Web n www.cellsignal.com rev. 06/16 #8579 For Research Use Only. Not For Use In Diagnostic Procedures. Products Included Product # Quantity Mol. Wt. Isotype Storage: Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% Phospho-YAP (Ser397) (D1E7Y) Rabbit mAb 13619 20 µl 75 kDa Rabbit IgG sodium azide. Store at –20°C. Do not aliquot the antibodies. LATS1 (C66B5) Rabbit mAb 3477 20 µl 140 kDa Rabbit IgG Recommended Antibody Dilutions: Western blotting 1:1000 Phospho-MOB1 (Thr35) (D2F10) Rabbit mAb 8699 20 µl 24 kDa Rabbit IgG Please visit www.cellsignal.com for validation data MOB1 (E1N9D) Rabbit mAb 13730 20 µl 25 kDa Rabbit IgG and a complete listing of recommended companion Mst1 Antibody 3682 20 µl 59 kDa Rabbit IgG products. Mst2 Antibody 3952 20 µl 60 kDa Rabbit IgG SAV1 (D6M6X) Rabbit mAb 13301 20 µl 45 kDa Rabbit IgG Phospho-YAP (Ser127) (D9W2I) Rabbit mAb 13008 20 µl 65-75 kDa Rabbit IgG YAP/TAZ (D24E4) Rabbit mAb 8418 20 µl 50,70 kDa Rabbit IgG Anti-rabbit IgG, HRP-linked Antibody 7074 100 µl Goat See www.cellsignal.com for individual component applications, species cross-reactivity, dilutions and additional application protocols. Description: The Hippo Signaling Antibody Sampler Kit MOB1 (Thr35) (D2F10) Rabbit mAb recognizes endogenous Background References: provides an economical means of detecting target proteins levels of MOB1 protein only when phosphorylated at Thr35. -
The Neurotransmitter Released at the Neuromuscular Junction Is
The Neurotransmitter Released At The Neuromuscular Junction Is Towney congeals his bibbers manipulate jocular, but cash-and-carry Winfred never extravasating so malcontentedly. Is Norton always dipetalous and unworn when guzzled some admeasurement very untidily and adversely? Busty Dominic overexcited some close and jemmying his galluses so nautically! Hiw are four nlgs are working memory, sv hubs depending on the specific to the neurotransmitter released neuromuscular junction at institutions across brain The energy is delivered in a fractional manner. Smooth muscle NMJ is formed between the autonomic nerve fibers that branch diffusely on strength muscle in form diffuse junctions. In an intact brain, volume was observed that Cac density at AZs is indeed strongly correlated with Pr. Chemical synapses involve the transmission of chemical information from one cell as the next. Currents through the fusion pore that forms during exocytosis of a secretory vesicle. If you order something abusive or that does not lessen with surrender terms or guidelines please flag it as inappropriate. Ach in the presynaptic protein in the active secretors of the released. You can login by using one alongside your existing accounts. Many drugs and anesthetic agents also affect neuromuscular junction and impulse transmission to inside their effects. The chemical must be present within a neuron. Another route for tetanus is lockjaw, respectively, the calcium rushes out of newly opened gates. In our data presented at multiple neurotransmitters are commonly performed by abnormal nmj but the neurotransmitter released at is the neuromuscular junction, it will fail to propagate from another power stroke can have qualitatively distinct categories reflective of the resultant of development. -
Hippo Signaling Interactions with Wnt/Β-Catenin and Notch Signaling Repress Liver Tumorigenesis
The Journal of Clinical Investigation RESEARCH ARTICLE Hippo signaling interactions with Wnt/β-catenin and Notch signaling repress liver tumorigenesis Wantae Kim,1,2 Sanjoy Kumar Khan,1,2 Jelena Gvozdenovic-Jeremic,1 Youngeun Kim,3 Jason Dahlman,1 Hanjun Kim,1,2 Ogyi Park,4 Tohru Ishitani,5 Eek-hoon Jho,3 Bin Gao,4 and Yingzi Yang1,2 1Genetic Disease Research Branch, National Human Genome Research Institute (NHGRI), NIH, Bethesda, Maryland, USA. 2Department of Developmental Biology, Harvard School of Dental Medicine (HSDM), Boston, Massachusetts, USA. 3Department of Life Sciences, University of Seoul, Seoul, South Korea. 4Section on Liver Biology, National Institute on Alcohol Abuse and Alcoholism (NIAAA), NIH, Bethesda, Maryland, USA. 5Division of Cell Regulation Systems, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan. Malignant tumors develop through multiple steps of initiation and progression, and tumor initiation is of singular importance in tumor prevention, diagnosis, and treatment. However, the molecular mechanism whereby a signaling network of interacting pathways restrains proliferation in normal cells and prevents tumor initiation is still poorly understood. Here, we have reported that the Hippo, Wnt/β-catenin, and Notch pathways form an interacting network to maintain liver size and suppress hepatocellular carcinoma (HCC). Ablation of the mammalian Hippo kinases Mst1 and Mst2 in liver led to rapid HCC formation and activated Yes-associated protein/WW domain containing transcription regulator 1 (YAP/TAZ), STAT3, Wnt/β-catenin, and Notch signaling. Previous work has shown that abnormal activation of these downstream pathways can lead to HCC. Rigorous genetic experiments revealed that Notch signaling forms a positive feedback loop with the Hippo signaling effector YAP/TAZ to promote severe hepatomegaly and rapid HCC initiation and progression. -
Role of Hippo Signaling Pathway in Early Placental Development COMMENTARY Francesca Soncina,B and Mana M
COMMENTARY Role of Hippo signaling pathway in early placental development COMMENTARY Francesca Soncina,b and Mana M. Parasta,b,1 The placenta is an organ of fetal origin that develops at the interface with the maternal uterus (1). It per- forms numerous and diverse functions fundamental for the proper growth and development of the semi- allogeneic fetus, including gas, nutrient, and waste exchange; production of hormones; and modulation of maternal immune response. Placental development begins, following implantation of the blastocyst-stage embryo, with the expansion of the trophectoderm (TE) and establishment of a villous trophoblast progenitor population, termed cytotrophoblast (CTB) (2). As this cell layer grows and invaginates to form chorionic villi (functional units of the human placenta), the CTB fur- ther expands and differentiates into two main mature trophoblast cell types: the syncytiotrophoblast (STB), involved in gas/nutrient exchange, and extravillous trophoblast (EVT), which invades the maternal decidua and remodels maternal spiral arterioles (Fig. 1). How- ever, the mechanisms behind early events in human Fig. 1. Human placental chorionic villus showing the different trophoblast placentation, particularly CTB self-renewal and differ- subtypes: vCTB, STB, and EVTs in the maternal decidua, the latter arising from entiation, are largely unknown. Using tools recently differentiation of vCTB through the cell column. Each placental trophoblast developed to study early human placental develop- subcompartment expresses different combinations of the TEAD family members ment, two studies in PNAS address the role of the and their transcriptional cofactors, YAP1, TAZ, and VGLL family members. This particular spatial expression pattern suggests a dynamic exchange of binding Hippo pathway in trophoblast progenitor self-renewal. -
The Hippo Signaling Pathway in Drug Resistance in Cancer
cancers Review The Hippo Signaling Pathway in Drug Resistance in Cancer Renya Zeng and Jixin Dong * Eppley Institute for Research in Cancer and Allied Diseases, Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE 68198, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-402-559-5596; Fax: +1-402-559-4651 Simple Summary: Although great breakthroughs have been made in cancer treatment following the development of targeted therapy and immune therapy, resistance against anti-cancer drugs remains one of the most challenging conundrums. Considerable effort has been made to discover the underlying mechanisms through which malignant tumor cells acquire or develop resistance to anti-cancer treatment. The Hippo signaling pathway appears to play an important role in this process. This review focuses on how components in the human Hippo signaling pathway contribute to drug resistance in a variety of cancer types. This article also summarizes current pharmacological interventions that are able to target the Hippo signaling pathway and serve as potential anti-cancer therapeutics. Abstract: Chemotherapy represents one of the most efficacious strategies to treat cancer patients, bringing advantageous changes at least temporarily even to those patients with incurable malignan- cies. However, most patients respond poorly after a certain number of cycles of treatment due to the development of drug resistance. Resistance to drugs administrated to cancer patients greatly limits the benefits that patients can achieve and continues to be a severe clinical difficulty. Among the mechanisms which have been uncovered to mediate anti-cancer drug resistance, the Hippo signaling pathway is gaining increasing attention due to the remarkable oncogenic activities of its components (for example, YAP and TAZ) and their druggable properties. -
STK3/4 Expression Is Regulated in Uterine Endometrial Cells During the Estrous Cycle
cells Article STK3/4 Expression Is Regulated in Uterine Endometrial Cells during the Estrous Cycle 1, 2, 2 1 1 3 Sohyeon Moon y, Ok-Hee Lee y, Sujin Lee , Jihyun Lee , Haeun Park , Miseon Park , Eun Mi Chang 3 , Keun-Hong Park 2 and Youngsok Choi 1,* 1 Department of Stem Cell and Regenerative Biotechnology, Humanized Pig Research Center, Konkuk University, Seoul 05029, Korea; [email protected] (S.M.); [email protected] (J.L.); [email protected] (H.P.) 2 Department of Biomedical Science, CHA University, Gyeonggi-do 13488, Korea; [email protected] (O.-H.L.); [email protected] (S.L.); [email protected] (K.-H.P.) 3 Fertility Center of CHA Gangnam Medical Center, CHA University, Seoul 06135, Korea; [email protected] (M.P.); [email protected] (E.M.C.) * Correspondence: [email protected]; Tel.: +82-2-450-3969 These authors contributed equally to this work. y Received: 16 October 2019; Accepted: 12 December 2019; Published: 15 December 2019 Abstract: The uterus is dynamically regulated in response to various signaling triggered by hormones during the estrous cycle. The Hippo signaling pathway is known as an important signaling for regulating cellular processes during development by balancing between cell growth and apoptosis. Serine/threonine protein kinase 3/4 (STK3/4) is a key component of the Hippo signaling network. However, the regulation of STK3/4-Hippo signaling in the uterus is little known. In this study, we investigated the regulation and expression of STK3/4 in the uterine endometrium during the estrous cycle. STK3/4 expression was dynamically regulated in the uterus during the estrous cycle. -
Multiple Roles for Cholinergic Signaling from the Perspective of Stem Cell Function
International Journal of Molecular Sciences Review Multiple Roles for Cholinergic Signaling from the Perspective of Stem Cell Function Toshio Takahashi Suntory Foundation for Life Sciences, Bioorganic Research Institute, Kyoto 619-0284, Japan; [email protected] Abstract: Stem cells have extensive proliferative potential and the ability to differentiate into one or more mature cell types. The mechanisms by which stem cells accomplish self-renewal provide fundamental insight into the origin and design of multicellular organisms. These pathways allow the repair of damage and extend organismal life beyond that of component cells, and they probably preceded the evolution of complex metazoans. Understanding the true nature of stem cells can only come from discovering how they are regulated. The concept that stem cells are controlled by particular microenvironments, also known as niches, has been widely accepted. Technical advances now allow characterization of the zones that maintain and control stem cell activity in several organs, including the brain, skin, and gut. Cholinergic neurons release acetylcholine (ACh) that mediates chemical transmission via ACh receptors such as nicotinic and muscarinic receptors. Although the cholinergic system is composed of organized nerve cells, the system is also involved in mammalian non-neuronal cells, including stem cells, embryonic stem cells, epithelial cells, and endothelial cells. Thus, cholinergic signaling plays a pivotal role in controlling their behaviors. Studies regarding this signal are beginning to unify our understanding of stem cell regulation at the cellular and molecular levels, and they are expected to advance efforts to control stem cells therapeutically. The present article reviews recent findings about cholinergic signaling that is essential to control stem cell function in a cholinergic niche.