Cilia length and motility regulation
Cilia are cellular organelles that protrude from almost every cell membrane. Cilia can be motile or immotile and can appear isolated or in bundles per cell. All types of cilia are thought to have signaling properties. Important signaling pathways during animal development and disease have been related to cilia, such as the Hedgehog, FGF and Notch signaling pathways. When cilia have defective length Hedgehog signaling is abnormal. On the other hand, Notch and FGF signaling defects trigger ciliary length and motility problems. We study cilia length and motility regulation in order to understand ciliopathies. We use the vertebrate zebrafish embryo because it has many ciliated organs with all cilia types and offers excellent imaging and genetic advantages.
Cilia have acquired major biomedical relevance due to the disclosure of many different diseases as ciliopathies i.e. diseases that have a ciliary origin. Ciliary protein defects underlie several human syndromes, such as Bardet-Biedl, Alstrom, Joubert, Senior-Løken, Meckel-Gruber, and Oral Facial Digit syndromes, that involve different conjugations of conditions such as polycystic kidney disease, retinal degeneration, anosmia, polydactyly, or organ situs reversal. Several of these syndromes show features not obviously related to cilia, including obesity and mental retardation. Human syndromes such as Kartagener were already identified as ciliopathies affecting motile cilia but many others such as Jeune asphyxiating thoracic dystrophy were not known as ciliopathies and have only recently been allocated to defects in primary cilia signaling. Ciliopathies affect many cell types and organs including kidney, liver, pancreas, heart, lungs, nose, ears, eyes and brain.
• Cilia length regulation.
• Cilia motility: beat frequency and pattern
• Cilia generated fluid flow dynamics within embryonic organs
• Ciliary mechano-sensory versus chemo-sensory signaling pathways
AWARD from Sociedade Portuguesa de Nefrologia
Project: Sphingolipid Signaling and CFTR stimulation in Autosomal Dominant Polycystic Kidney Disease
Team: Mónica Roxo-Rosa (PI), Susana Lopes, Bárbara Tavares and Joaquim Calado (ToxOmics)
LYSOCIL: Excel in Rare Diseases’ Research: Focus on LYSOsomal Disorders and CILiopathies
01/11/2018 – 30/04/2022
European Union’s Horizon Twinning project 2020 (No 811087)
LYSOCIL is a Twinning Project led by NOVA Medical School (NMS) that aims to strengthen the research and innovation capacity of the Chronic Diseases Research Center (CEDOC-NMS|FCM) in research in rare diseases, helping it to become a national and internationally-recognized centre of excellence in chronic rare diseases research and innovation. For this project, CEDOC-NMS|FCM partnered up with two internationally-leading institutions, Münster University (WWU), a German institution with a strong research profile in basic, clinical and translational medicine connected to rare diseases, and the Telethon Institute of Genetics and Medicine (TIGEM), the leading Italian research center dedicated to understanding the molecular mechanisms behind rare genetic diseases. This partnership will boost the multidisciplinary knowledge and experience, as well as research and training practices and widen the collaborative networks to step up the excellence of the research of the involved partners. Our research group is a partner in this project.
Principal Investigators: Duarte Barral and Susana Lopes
Research on left-right development
This is the main branch of my lab. We have been investigating the role of time in the left-right organizer (LRO). This ciliated embryonic organ is crucial for determining the laterality identity of the vertebrate body-plan. This organ has exciting biophysical properties that control several mechanisms of development, making it an interesting and relevant area of investigation. Namely, biophysical fluid-flow forces that will be translated into gene expression, and determine the location of the future heart on the left and the liver on the right side of the midline axis. Such fluid-flow is directional and known to be generated by motile cilia (Sampaio et al. Dev Cell. 2014). This flow starts by being mild and later becoming strong due to an increase in motile cilia number (Tavares et al. eLIFE. 2017). As a consequence, in the LRO there are two distinct time-windows underlying two fluid-flow regimes. Our current research investigates the molecular mechanisms behind these time-windows by integrating developmental biology, genetics, live-imaging, and bespoke fluid-mechanics modelling in collaboration with the University of Birmingham (Smith et al. Bioarchitecture, 2014; Montenegro-Johnson et al. J Math Biol. 2016; Pintado et al. R. Soc. open sci. 2017).
Research on Primary Ciliary Dyskinesia
The second interest of my lab, still related to left-right development, is the rare disease Primary Ciliary Dyskinesia (PCD), a disease where 50% of the patients develop situs inversus, i.e reversal of the internal organs. Like in most countries, PCD was not properly diagnosed in Portugal. Within the context of COST Beat-PCD-BM1407, my team learned and implemented some of the required techniques according to the European guidelines for PCD. We next triggered the implementation of a Lisbon PCD consortium so that, together with the Hospital Sta Maria (HSM, Lisbon) and Instituto de Medicina Molecular (IMM, Lisbon)), we can currently provide a robust multidisciplinary diagnostic according to the recent requirements for PCD. Our lab performs high-speed videomicroscopy analysis, necessary for the evaluation of cilia beat frequency and pattern (Constant et al. 2018. Acta Pediátrica Portuguesa). As a consequence of PCD diagnostics we started a new area of research in the lab. So far, we have invested on making better diagnostic software for cilia analysis in collaboration with Carla Quintão (NOVA, FCT). Additionally, we have generated zebrafish PCD genetic mutants by using CRISPR-Cas9 gene editing to mimic and better dissect mutations found in patients. The final aim is to rescue some cilia function in patients using gene therapy in collaboration with the Omran lab (WWU, Germany), with whom we have recently been funded by H2020-WIDESPREAD-2016-2017 in the format of a Twinning project, named Lysocil, to improve research on rare diseases in Portugal, including ciliopathies.
Research on Delta-Notch signalling
This signaling pathway is important for ciliary length regulation as well as for deciding the number of motile cilia. We investigated how is DeltaD linked to ciliogenesis and its impact on left-right development (Lopes et al. Development. 2010). This project carried on and we have now identified many interesting genes that are differentially expressed in zebrafish wild-type embryos and deltaD homozygous mutants. Our aim is to understand what are the genes downstream of the Delta-Notch signaling that can rescue cilia length and motility. A recent article from our lab summarizes this branch of our research: ‘Notch/Her12 signalling modulates motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer’ (Tavares et al. eLIFE. 2017). We will continue searching for Her12 effector genes involved in this fate process.
Research on Pkd2 signalling
This cation channel is thought to partner with Pkd1l1 and sense ‘nodal flow’, an important feature in left-right development. We ask if having no flow has the same impact as having no Pkd2-mediated sensing. We realized this question is much harder to answer then we thought and we are generating new methods to tackle this question. Most interesting, this question led us to another perhaps more fascinating problem which is, how does the embryo try to rescue a defective ‘nodal flow’ during early left-right development?
- Pkd2 Affects Cilia Length and Impacts LR Flow Dynamics and Dand5. Raquel Jacinto, Pedro Sampaio, Mónica Roxo-Rosa, Sara Pestana, Susana Lopes. Front. Cell Dev. Biol. 9, 624531; DOI: 10.3389/fcell.2021.624531. Published 1 April 2021
- CiliarMove: new software for evaluating ciliary beat frequency helps find novel mutations by a Portuguese multidisciplinary team on primary ciliary dyskinesia. Pedro Sampaio, Mónica Ferro da Silva, Inês Vale, Mónica Roxo-Rosa, Andreia Pinto, Carolina Constant, Luisa Pereira, Carla M. Quintão, Susana S. Lopes. ERJ Open Res 7: 00792-2020; DOI: 10.1183/23120541.00792-2020 Published 8 February 2021
- Unmasking the relevance of hemispheric asymmetries-Break on through (to the other side). Esteves M, Lopes SS, Almeida A, Sousa N, Leite-Almeida H. Prog Neurobiol. 2020 Sep;192:101823. doi: 10.1016/j.pneurobio.2020.101823. Epub 2020 May 17.
- Fassad MR, Patel MP, Shoemark A, Cullup T, Hayward J, Dixon M, Rogers AV, Ollosson S, Jackson C, Goggin P, Hirst RA, Rutman A, Thompson J, Jenkins L, Aurora P, Moya E, Chetcuti P, O'Callaghan C, Morris-Rosendahl DJ, Watson CM, Wilson R, Carr S, Walker W, Pitno A, Lopes S, Morsy H, Shoman W, Pereira L, Constant C, Loebinger MR, Chung EMK, Kenia P, Rumman N, Fasseeh N, Lucas JS, Hogg C, Mitchison HM. Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliarydyskinesia cohort. J Med Genet. 2019 Dec 25. pii: jmedgenet-2019-106501. doi: 10.1136/jmedgenet-2019-106501. [Epub ahead of print]
- Burkhalter MD, Sridhar A, Sampaio P, Jacinto R, Burczyk MS, Donow C, Angenendt M; Competence Network for Congenital Heart Defects Investigators, Hempel M5, Walther P, Pennekamp P, Omran H, Lopes SS, Ware SM, Philipp M. Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis. J Clin Invest. 2019 May 16;130:2841-2855. doi: 10.1172/JCI98890.
- Solowiej-Wedderburn J, Smith DJ, Lopes SS, Montenegro-Johnson TD (2018) Wall stress enhanced exocytosis of extracellular vesicles as a possible mechanism of left-right symmetry-breaking in vertebrate development. Journal of Theoretical Biology (2018), doi:https://doi.org/10.1016/j.jtbi.2018.10.015
- Morello J, Derks RJE, Lopes SS, Steenvoorden E, Monteiro EC, Mayboroda OA, Pereira SA (2018) Zebrafish Larvae Are a Suitable Model to Investigate the Metabolic Phenotype of Drug-Induced Renal Tubular Injury. Front. Pharmacol. 9:1193. doi: 10.3389/fphar.2018.01193
- C. Constant, R. Sousa, A. Pinto, J.F. Moura Nunes, P. Sampaio, SS. Lopes, T. Bandeira and L. Pereira (2017) New era in Primary Ciliary Dyskinesia diagnosis. Accepted on the 16th November 2017
- Gorgulho R, Jacinto R, Lopes SS, Pereira SA, Tranfield EM, Martins GG, Gualda EJ, Derks RJE, Correia AC, Steenvoorden E, Pintado P, Mayboroda OA, Monteiro EC, Morello J (2017) Usefulness of zebrafish larvae to evaluate drug-induced functional and morphological renal tubular alterations. Arch Toxicol. 2017 Sep 20. doi: 10.1007/s00204-017-2063-1
- B. Tavares, R. Jacinto, P. Sampaio, S. Pestana, A. Pinto, A. Vaz, M. Roxo-Rosa, R. Gardner, T. Lopes, B. Schilling, I. Henry, L. Saúde and S.S. Lopes (2017) Notch/Her12 signalling modulates motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer. eLife 2017;6:e25165 doi: 10.7554/eLife.25165
- P. Pintado, P. Sampaio, B. Tavares, T. D. Montenegro-Johnson, D. J. Smith, S. S. Lopes (2017) Dynamics of cilia length in left–right development. R. Soc. open sci. 2017 4 161102; DOI: 10.1098/rsos.161102
- Lopes SS, Distel M, Linker C, Fior R, Monteiro R, Bianco IH, Portugues R, Strähle U, Saúde L. (2016) Report of the 4th European Zebrafish Principal Investigator Meeting. Zebrafish. 2016 Sep 14. [Epub ahead of print]
- T.D Montenegro-Johnson, D.I. Baker, D.J. Smith and S.S. Lopes. (2016) Three-dimensional flow in Kupffer’s Vesicle. J. Math Biol. Online 29 January 2016. doi: 10.1007/s00285-016-0967-7.
- Monica Roxo-Rosa, Raquel Jacinto, Pedro Sampaio, and Susana Santos Lopes (2015) The zebrafish Kupffer' s vesicle as a model system for the molecular mechanisms by which the lack of Polycystin-2 leads to stimulation of CFTR. Biol Open. 2015 Oct 2. pii: bio.014076. doi: 10.1242/bio.014076. [Epub ahead of print]
- Quanlong Lu, Christine Insinna, Carolyn Ott, Jimmy Stauffer, Petra Pintado, Juliati Rahajeng, Ulrich Baxa, Vijay Walia, Adrian Cuenca, Yoo-Seok Hwang, Ira Daar, Susana S. Lopes, Jennifer Lippincott-Schwartz, Peter Jackson, Steve Caplan, and Christopher Westlake (2015) Early steps in primary cilium assembly require EHD1/EHD3-dependent ciliary vesicle formation. NNat Cell Biol. 2015 Mar;17(3):228-40. doi: 10.1038/ncb3109. Epub 2015 Feb 16.
- Sampaio P, Ferreira RR, Guerrero A, Pintado P, Tavares B, Amaro J, Smith AA,Montenegro-Johnson T, Smith DJ, Lopes SS. (2014) Left-Right Organizer Flow Dynamics: How Much Cilia Activity Reliably Yields Laterality? Dev Cell. pii: S1534-5807(14)00277-9. doi: 10.1016/j.devcel.2014.04.030.
- Smith Dj, Montenegro-Johnson T, Lopes S.S. (2014) Organized chaos in Kupffer's vesicle: How a heterogeneous structure achieves consistent left-right patterning. May-Jun;4(3):119-25. Bioarchitecture doi: 10.4161/19490992.2014.956593.
- Cristina Casalou, Cecília Seixas, Ana Portelinha, Petra Pintado, Mafalda Barros, José S Ramalho, Susana S Lopes, Duarte C Barral (2014) Arl13b and the non-muscle myosin heavy chain IIA are required for circular dorsal ruffle formation and cell migration. Journal of cell science, jcs. 143446
- Tavares B, Santos Lopes S. (2013) The Importance of Zebrafish in Biomedical Research. Acta Med Port., 26(5):583-592. Epub 2013 Oct 31.
- Lourenço R, Lopes SS, Saúde L. Left-right function of dmrt2 genes is not conserved between zebrafish and mouse. PLoS One. 2010 Dec 28;5(12):e14438. PMID:21203428
- Lopes SS, Lourenço R, Pacheco L, Moreno N, Kreiling J, Saúde L. Notch signalling regulates left-right asymmetry through ciliary length control. Development. 2010 Nov;137(21):3625-32. Epub 2010 Sep 28. PMID: 20876649
- Rocha SF, Lopes SS, Gossler A, Henrique D. Dll1 and Dll4 function sequentially in the retina and pV2 domain of the spinal cord to regulate neurogenesis and create cell diversity. Dev Biol. 2009 Apr 1;328(1):54-65. Epub 2009 Jan 14. PMID: 19389377
- Lopes SS, Yang X, Müller J, Carney TJ, McAdow AR, Rauch GJ, Jacoby AS, Hurst LD, Delfino-Machín M, Haffter P, Geisler R, Johnson SL, Ward A, Kelsh RN. Leukocyte tyrosine kinase functions in pigment cell development. PLoS Genet. 2008 Mar 7;4(3):e1000026. PMID:18369445
- Dutton KA, Pauliny A, Lopes SS, Elworthy S, Carney TJ, Rauch J, Geisler R, Haffter P, Kelsh RN. Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates. Development. 2001 Nov;128(21):4113-25. PMID: 11684650
- Parichy DM, Mellgren EM, Rawls JF, Lopes SS, Kelsh RN, Johnson SL. Mutational analysis of endothelin receptor b1 (rose) during neural crest and pigment pattern development in the zebrafish Danio rerio. Dev Biol. 2000 Nov 15;227(2):294-306. PMID: 11071756
- Ivo Telley - Micromanipulations and fluidics. Instituto Gulbenkian Ciência, Oeiras
- Adan Guerrero - 3D flow Imaging. Instituto Gulbenkian de Ciência, Oeiras
- Thomas Johnson-Montenegro - Simulations for cilia beating and flow. School of Mathematics, U. of Birmingham, UK
- Christopher Westlake - Primary cilium assembly. NCI-Frederick National Laboratory, USA
- David Smith - Simulations fluid flow. School of Mathematics, U. of Birmingham, UK
- Carla Quintão - Software. Department of Physics from FCT-NOVA, Portugal
- Duarte Barral - Cellular Traffic. CEDOC. NOVA Medical School. Portugal
- Paulo Pereira - Exosome biology. CEDOC. NOVA Medical School. Portugal
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