200 research outputs found

    Pericellular Innervation of Neurons Expressing Abnormally Hyperphosphorylated Tau in the Hippocampal Formation of Alzheimer's Disease Patients

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    Neurofibrillary tangles (NFT) represent one of the main neuropathological features in the cerebral cortex associated with Alzheimer's disease (AD). This neurofibrillary lesion involves the accumulation of abnormally hyperphosphorylated or abnormally phosphorylated microtubule-associated protein tau into paired helical filaments (PHF-tau) within neurons. We have used immunocytochemical techniques and confocal microscopy reconstructions to examine the distribution of PHF-tau-immunoreactive (ir) cells, and their perisomatic GABAergic and glutamatergic innervations in the hippocampal formation and adjacent cortex of AD patients. Furthermore, correlative light and electron microscopy was employed to examine these neurons and the perisomatic synapses. We observed two patterns of staining in PHF-tau-ir neurons, pattern I (without NFT) and pattern II (with NFT), the distribution of which varies according to the cortical layer and area. Furthermore, the distribution of both GABAergic and glutamatergic terminals around the soma and proximal processes of PHF-tau-ir neurons does not seem to be altered as it is indistinguishable from both control cases and from adjacent neurons that did not contain PHF-tau. At the electron microscope level, a normal looking neuropil with typical symmetric and asymmetric synapses was observed around PHF-tau-ir neurons. These observations suggest that the synaptic connectivity around the perisomatic region of these PHF-tau-ir neurons was apparently unaltered

    Plant vascular development: mechanisms and environmental regulation

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    [EN] Plant vascular development is a complex process culminating in the generation of xylem and phloem, the plant transporting conduits. Xylem and phloem arise from specialized stem cells collectively termed (pro)cambium. Once developed, xylem transports mainly water and mineral nutrients and phloem transports photoassimilates and signaling molecules. In the past few years, major advances have been made to characterize the molecular, genetic and physiological aspects that govern vascular development. However, less is known about how the environment re-shapes the process, which molecular mechanisms link environmental inputs with developmental outputs, which gene regulatory networks facilitate the genetic adaptation of vascular development to environmental niches, or how the first vascular cells appeared as an evolutionary innovation. In this review, we (1) summarize the current knowledge of the mechanisms involved in vascular development, focusing on the model species Arabidopsis thaliana, (2) describe the anatomical effect of specific environmental factors on the process, (3) speculate about the main entry points through which the molecular mechanisms controlling of the process might be altered by specific environmental factors, and (4) discuss future research which could identify the genetic factors underlying phenotypic plasticity of vascular development.Work in the authors' laboratories is supported by funds from the Spanish Ministry of Science and Universities (BIO2016-79147-R to JA, and BFU2016-80621-P to MAB). JA holds a Ramon y Cajal contract (RYC-2014-15752). We are deeply grateful to Debra Westall (Universitat Politecnica de Valencia) for revising the manuscript. Due to space limitations, not all relevant publications could be included in this review.Agustí, J.; Blazquez Rodriguez, MA. (2020). Plant vascular development: mechanisms and environmental regulation. Cellular and Molecular Life Sciences. 77(19):1-18. https://doi.org/10.1007/s00018-020-03496-wS1187719Bowman JL, Kohchi T, Yamato KT, Jenkins J, Shu S, Ishizaki K et al (2017) Insights into land plant evolution garnered from the Marchantia polymorpha genome. Cell 171(2):287–304. https://doi.org/10.1016/j.cell.2017.09.030(Epub 2017/10/07. PubMed PMID: 28985561)Lucas WJ, Groover A, Lichtenberger R, Furuta K, Yadav SR, Helariutta Y et al (2013) The plant vascular system: evolution, development and functions. J Integr Plant Biol 55(4):294–388. https://doi.org/10.1111/jipb.12041(Epub 2013/03/07. PubMed PMID: 23462277)Nelson T, Dengler N (1997) Leaf vascular pattern formation. Plant Cell 9(7):1121–1135. https://doi.org/10.1105/tpc.9.7.1121(Epub 1997/07/01. PubMed PMID: 12237378; PubMed Central PMCID: PMCPMC156985)Agusti J, Greb T (2013) Going with the wind-adaptive dynamics of plant secondary meristems. Mech Dev 130(1):34–44. https://doi.org/10.1016/j.mod.2012.05.011(Epub 2012/06/14. PubMed PMID: 22691403; PubMed Central PMCID: PMCPMC3560032)Esau K (1961) Anatomy of seed plants. Wiley, New YorkSpicer R, Groover A (2010) Evolution of development of vascular cambia and secondary growth. New Phytol 186(3):577–592. https://doi.org/10.1111/j.1469-8137.2010.03236.xRuonala R, Ko D, Helariutta Y (2017) Genetic networks in plant vascular development. Annu Rev Genet 51:335–359. https://doi.org/10.1146/annurev-genet-120116-024525(Epub 2017/09/12. PubMed PMID: 28892639)Cano-Delgado A, Lee JY, Demura T (2010) Regulatory mechanisms for specification and patterning of plant vascular tissues. Annu Rev Cell Dev Biol 26:605–637. https://doi.org/10.1146/annurev-cellbio-100109-104107(Epub 2010/07/02. PubMed PMID: 20590454)Berleth T, Jurgens G (1993) The role of the monopteros gene in organising the basal body region of the Arabidopsis embryo. Development 118(2):575–587Hartke CS, Berleth T (1998) The Arabidopsis gene MONOPTEROS encodes a transcription factor mediating embryo axis formation and vascular development. EMBO J 17:1405–1411Busse JS, Evert RF (1999) Pattern of differentiation of the first vascular elements in the embryo and seedling of Arabidopsis thaliana. Int J Plant Sci 160:1–13Mayer U, Ruiz RAT, Berleth T, Miséra S, Jürgens G (1991) Mutations affecting body organization in the Arabidopsis embryo. Nature 353(6343):402–407. https://doi.org/10.1038/353402a0Wenzel CL, Schuetz M, Yu Q, Mattsson J (2007) Dynamics of MONOPTEROS and PIN-FORMED1 expression during leaf vein pattern formation in Arabidopsis thaliana. Plant J 49(3):387–398. https://doi.org/10.1111/j.1365-313X.2006.02977.x(Epub 2007/01/16. PubMed PMID: 17217464)Weijers D, Schlereth A, Ehrismann JS, Schwank G, Kientz M, Jurgens G (2006) Auxin triggers transient local signaling for cell specification in Arabidopsis embryogenesis. Dev Cell 10(2):265–270. https://doi.org/10.1016/j.devcel.2005.12.001(Epub 2006/02/07. PubMed PMID: 16459305)Hamann T, Benkova E, Baurle I, Kientz M, Jurgens G (2002) The Arabidopsis BODENLOS gene encodes an auxin response protein inhibiting MONOPTEROS-mediated embryo patterning. Genes Dev 16(13):1610–1615. https://doi.org/10.1101/gad.229402(Epub 2002/07/09. PubMed PMID: 12101120; PubMed Central PMCID: PMCPMC186366)Hamann T, Mayer U, Jurgens G (1999) The auxin-insensitive bodenlos mutation affects primary root formation and apical-basal patterning in the Arabidopsis embryo. Development 126(7):1387–1395 (Epub 1999/03/09. PubMed PMID: 10068632)Kepinski S, Leyser O (2005) The Arabidopsis F-box protein TIR1 is an auxin receptor. Nature 435(7041):446–451. https://doi.org/10.1038/nature03542(Epub 2005/05/27. PubMed PMID: 15917798)Schlereth A, Moller B, Liu W, Kientz M, Flipse J, Rademacher EH et al (2010) MONOPTEROS controls embryonic root initiation by regulating a mobile transcription factor. Nature 464(7290):913–916. https://doi.org/10.1038/nature08836(Epub 2010/03/12. PubMed PMID: 20220754)Rashotte AM, Mason MG, Hutchison CE, Ferreira FJ, Schaller GE, Kieber JJ (2006) A subset of Arabidopsis AP2 transcription factors mediates cytokinin responses in concert with a two-component pathway. Proc Natl Acad Sci USA 103(29):11081–11085. https://doi.org/10.1073/pnas.0602038103(Epub 2006/07/13. PubMed PMID: 16832061; PubMed Central PMCID: PMCPMC1544176)Rybel De B, Moller B, Yoshida S, Grabowicz I, Barbier de Reuille P, Boeren S et al (2013) A bHLH complex controls embryonic vascular tissue establishment and indeterminate growth in Arabidopsis. Dev Cell 24(4):426–437. https://doi.org/10.1016/j.devcel.2012.12.013(Epub 2013/02/19. PubMed PMID: 23415953)Vera-Sirera F, Rybel De B, Urbez C, Kouklas E, Pesquera M, Alvarez-Mahecha JC et al (2015) A bHLH-based feedback loop restricts vascular cell proliferation in plants. Dev Cell 35(4):432–443. https://doi.org/10.1016/j.devcel.2015.10.022(Epub 2015/11/27. PubMed PMID: 26609958)Miyashima S, Roszak P, Sevilem I, Toyokura K, Blob B, Heo JO et al (2019) Mobile PEAR transcription factors integrate positional cues to prime cambial growth. Nature 565(7740):490–494. https://doi.org/10.1038/s41586-018-0839-y(Epub 2019/01/11. PubMed PMID: 30626969)Mahonen AP, Bonke M, Kauppinen L, Riikonen M, Bengey PN, Helariutta Y (2000) A novel two-component hybrid molecule regulates vascular morphogenesis of the Arabidopsis root. Genes Dev 14:2938–2943Baum SF, Dubrovsky JG, Rost TL (2002) Apical organization and maturation of the cortex and vascular cylonder in Arabidopsis thaliana (Brassicaceae) roots. Am J Bot 89(6):908–920Campbell L, Turner S (2017) Regulation of vascular cell division. J Exp Bot 68(1):27–43. https://doi.org/10.1093/jxb/erw448(Epub 2016/12/15. PubMed PMID: 27965363)Dolan L, Janmaat K, Willemsen V, Linstead P, Poethig S, Roberts K, Scheres B (1993) Cellular organisation of the Arabidopsis thaliana root. Development 119(1):71–84Mellor N, Adibi M, El-Showk S, Rybel De B, King J, Mahonen AP et al (2017) Theoretical approaches to understanding root vascular patterning: a consensus between recent models. J Exp Bot 68(1):5–16. https://doi.org/10.1093/jxb/erw410(Epub 2016/11/12. PubMed PMID: 27837006)Carlsbecker A, Lee JY, Roberts CJ, Dettmer J, Lehesranta S, Zhou J et al (2010) Cell signalling by microRNA165/6 directs gene dose-dependent root cell fate. Nature 465(7296):316–321. https://doi.org/10.1038/nature08977(Epub 2010/04/23. PubMed PMID: 20410882; PubMed Central PMCID: PMCPMC2967782)Ramachandran P, Wang G, Augstein F, Vries de J, Carlsbecker A (2018) Continuous root xylem formation and vascular acclimation to water deficit involves endodermal ABA signalling via miR165. Development. https://doi.org/10.1242/dev.159202(Epub 2018/01/24. PubMed PMID: 29361572)Mahonen AP, Bishopp A, Higuchi M, Nieminen KM, Kinoshita K, Tormakangas K, Ikeda Y, Oka A, Kakimoto T, Helariutta Y (2006) Cytokinin signaling and its inhibitor AHP6 regulate cell fate during vascular development. Science 311:94–98Mahonen AP, Higuchi M, Tormakangas K, Miyawaki K, Pischke MS, Sussman MR et al (2006) Cytokinins regulate a bidirectional phosphorelay network in Arabidopsis. Curr Biol 16(11):1116–1122. https://doi.org/10.1016/j.cub.2006.04.030(Epub 2006/06/07. PubMed PMID: 16753566)Ohashi-Ito K, Saegusa M, Iwamoto K, Oda Y, Katayama H, Kojima M et al (2014) A bHLH complex activates vascular cell division via cytokinin action in root apical meristem. Curr Biol 24(17):2053–2058. https://doi.org/10.1016/j.cub.2014.07.050(Epub 2014/08/19. PubMed PMID: 25131670)Bishopp A, Lehesranta S, Vaten A, Help H, El-Showk S, Scheres B et al (2011) Phloem-transported cytokinin regulates polar auxin transport and maintains vascular pattern in the root meristem. Curr Biol 21(11):927–932. https://doi.org/10.1016/j.cub.2011.04.049(Epub 2011/05/31. PubMed PMID: 21620705)Bishopp A, Help H, El-Showk S, Weijers D, Scheres B, Friml J et al (2011) A mutually inhibitory interaction between auxin and cytokinin specifies vascular pattern in roots. Curr Biol 21(11):917–926. https://doi.org/10.1016/j.cub.2011.04.017(Epub 2011/05/31. PubMed PMID: 21620702)Rybel De B, Adibi M, Breda AS, Wendrich JR, Smit ME, Novak O et al (2014) Integration of growth and patterning during vascular tissue formation in Arabidopsis. Science 345(6197):1255215. https://doi.org/10.1126/science.1255215(Epub 2014/08/12. PubMed PMID: 25104393)Knott JM (2009) Biosynthesis of long-chain polyamines by crenarchaeal polyamine synthases from Hyperthermus butylicus and Pyrobaculum aerophilum. FEBS Lett 583(21):3519–3524. https://doi.org/10.1016/j.febslet.2009.10.014(Epub 2009/10/14. PubMed PMID: 19822146)Knott JM, Romer P, Sumper M (2007) Putative spermine synthases from Thalassiosira pseudonana and Arabidopsis thaliana synthesize thermospermine rather than spermine. FEBS Lett 581(16):3081–3086. https://doi.org/10.1016/j.febslet.2007.05.074(Epub 2007/06/15. PubMed PMID: 17560575)Baima S, Forte V, Possenti M, Penalosa A, Leoni G, Salvi S et al (2014) Negative feedback regulation of auxin signaling by ATHB8/ACL5-BUD2 transcription module. Mol Plant 7(6):1006–1025. https://doi.org/10.1093/mp/ssu051(Epub 2014/04/30. PubMed PMID: 24777988)Imai A, Hanzawa Y, Komura M, Yamamoto KT, Komeda Y, Takahashi T (2006) The dwarf phenotype of the Arabidopsis acl5 mutant is suppressed by a mutation in an upstream ORF of a bHLH gene. Development 133(18):3575–3585. https://doi.org/10.1242/dev.02535(Epub 2006/08/29. PubMed PMID: 16936072)Katayama H, Iwamoto K, Kariya Y, Asakawa T, Kan T, Fukuda H et al (2015) A negative feedback loop controlling bHLH complexes is involved in vascular cell division and differentiation in the root apical meristem. Curr Biol 25(23):3144–3150. https://doi.org/10.1016/j.cub.2015.10.051(Epub 2015/12/01. PubMed PMID: 26616019)Muniz L, Minguet EG, Singh SK, Pesquet E, Vera-Sirera F, Moreau-Courtois CL et al (2008) ACAULIS5 controls Arabidopsis xylem specification through the prevention of premature cell death. Development 135(15):2573–2582. https://doi.org/10.1242/dev.019349(Epub 2008/07/05. PubMed PMID: 18599510)Milhinhos A, Prestele J, Bollhöner B, Matos A, Vera-Sirera F, Rambla JL et al (2013) Thermospermine levels are controlled by an auxin-dependent feedback loop mechanism in Populus xylem. Plant J 75(4):685–698Sole-Gil A, Hernandez-Garcia J, Lopez-Gresa MP, Blazquez MA, Agusti J (2019) Conservation of thermospermine synthase activity in vascular and non-vascular plants. Front Plant Sci 10:663. https://doi.org/10.3389/fpls.2019.00663(Epub 2019/06/28. PubMed PMID: 31244864; PubMed Central PMCID: PMCPMC6579911)Bonke M, Thitamadee S, Mahonen AP, Hauser MT, Helariutta Y (2003) APL regulates vascular tissue identity in Arabidopsis. Nature 426(6963):181–186. https://doi.org/10.1038/nature02100(Epub 2003/11/14. PubMed PMID: 14614507)Truernit E, Bauby H, Dubreucq B, Grandjean O, Runions J, Barthelemy J et al (2008) High-resolution whole-mount imaging of three-dimensional tissue organization and gene expression enables the study of phloem development and structure in Arabidopsis. Plant Cell 20(6):1494–1503. https://doi.org/10.1105/tpc.107.056069(Epub 2008/06/05. PubMed PMID: 18523061; PubMed Central PMCID: PMCPMC2483377)Furuta KM, Yadav SR, Lehesranta S, Belevich I, Miyashima S, Heo JO et al (2014) Plant development. Arabidopsis NAC45/86 direct sieve element morphogenesis culminating in enucleation. Science 345(6199):933–937. https://doi.org/10.1126/science.1253736(Epub 2014/08/02. PubMed PMID: 25081480)Kondo Y, Nurani AM, Saito C, Ichihashi Y, Saito M, Yamazaki K, Mitsuda N, Ohme-Takagi M, Fukuda H (2016) Vascular cell induction culture system using Arabidopsis leaves (VISUAL) reveals the sequential differentiation of sieve element-like cells. Plant Cell 28(6):1250–1262. https://doi.org/10.1105/tpc.16.00027Truernit E, Bauby H, Belcram K, Barthelemy J, Palauqui JC (2012) OCTOPUS, a polarly localised membrane-associated protein, regulates phloem differentiation entry in Arabidopsis thaliana. Development 139(137):1306–1315. https://doi.org/10.1242/dev.072629(Epub 2012/03/08. PubMed PMID: 22395740)Mouchel CF, Briggs GC, Hardtke CS (2004) Natural genetic variation in Arabidopsis identifies BREVIS RADIX, a novel regulator of cell proliferation and elongation in the root. Genes Dev 18(6):700–714. https://doi.org/10.1101/gad.1187704(Epub 2004/03/20. PubMed PMID: 15031265; PubMed Central PMCID: PMCPMC387244)Rodriguez-Villalon A, Gujas B, Kang YH, Breda AS, Cattaneo P, Depuydt S et al (2014) Molecular genetic framework for protophloem formation. Proc Natl Acad Sci USA 111(31):11551–11556. https://doi.org/10.1073/pnas.1407337111(Epub 2014/07/23. PubMed PMID: 25049386; PubMed Central PMCID: PMCPMC4128119)Marhava P, Bassukas AEL, Zourelidou M, Kolb M, Moret B, Fastner A et al (2018) A molecular rheostat adjusts auxin flux to promote root protophloem differentiation. Nature 558(7709):297–300. https://doi.org/10.1038/s41586-018-0186-z(Epub 2018/06/08. PubMed PMID: 29875411)Depuydt S, Rodriguez-Villalon A, Santuari L, Wyser-Rmili C, Ragni L, Hardtke CS (2013) Suppression of Arabidopsis protophloem differentiation and root meristem growth by CLE45 requires the receptor-like kinase BAM3. Proc Natl Acad Sci USA 110(17):7074–7079. https://doi.org/10.1073/pnas.1222314110(Epub 2013/04/10. PubMed PMID: 23569225; PubMed Central PMCID: PMCPMC3637694)Kang YH, Hardtke CS (2016) Arabidopsis MAKR5 is a positive effector of BAM3-dependent CLE45 signaling. EMBO Rep 17(8):1145–1154. https://doi.org/10.15252/embr.201642450(Epub 2016/06/30. PubMed PMID: 27354416; PubMed Central PMCID: PMCPMC4967951)Breda AS, Hazak O, Schultz P, Anne P, Graeff M, Simon R et al (2019) Cellular insulator against CLE45 peptide signaling. Curr Biol 29(15):2501–2508. https://doi.org/10.1016/j.cub.2019.06.037(Epub 2019/07/23. PubMed PMID: 31327718)Rodriguez-Villalon A, Gujas B, Wijk van R, Munnik T, Hardtke CS (2015) Primary root protophloem differentiation requires balanced phosphatidylinositol-4,5-biphosphate levels and systemically affects root branching. Development 142(8):1437–1446. https://doi.org/10.1242/dev.118364(Epub 2015/03/31. PubMed PMID: 25813544)Gujas B, Cruz TMD, Kastanaki E, Vermeer JEM, Munnik T, Rodriguez-Villalon A (2017) Perturbing phosphoinositide homeostasis oppositely affects vascular differentiation in Arabidopsis thaliana roots. Development 144(19):3578–3589. https://doi.org/10.1242/dev.155788(Epub 2017/08/31. PubMed PMID: 28851711; PubMed Central PMCID: PMCPMC5665488)Wallner E-S, Lopez-Salmeron V, Belevich I, Poschet G, Jung I, Grunwald K, Sevilem I, Jokitalo E, Hell R, Helariutta Y, Agusti J, Lebovka I, Greb T (2017) Strigolactone- and karrikin-independent SMXL proteins are central regulators of phloem formation. Curr Biol 27:1241–1247Hickey LJ (1973) Classification of the architecture of dicotyledonous leaves. Am J Bot 60(1):17–33Sachs T (1981) The control of the patterned differentiation of vascular tissues. Adv Bot Res 9:151–162Sachs T (1989) The development of vascular networks during leaf development. Curr Top Plant Biochem Physiol 8:168–183Mattsson J, Ckurshumova W, Berleth T (2003) Auxin signaling in Arabidopsis leaf vascular development. Plant Physiol 131(3):1327–1339. https://doi.org/10.1104/pp.013623(Epub 2003/03/20. PubMed PMID: 12644682; PubMed Central PMCID: PMCPMC166892)Scarpella E, Marcos D, Friml J, Berleth T (2006) Control of leaf vascular patterning by polar auxin transport. Genes Dev 20(8):1015–1027. https://doi.org/10.1101/gad.1402406(Epub 2006/04/19. PubMed PMID: 16618807; PubMed Central PMCID: PMCPMC1472298)Donner TJ, Sherr I, Scarpella E (2009) Regulation of preprocambial cell state acquisition by auxin signaling in Arabidopsis leaves. Development 136(19):3235–3246. https://doi.org/10.1242/dev.037028(Epub 2009/08/28. PubMed PMID: 19710171)Emery JF, Floyd SK, Alvarez J, Eshed Y, Hawker NP, Izhaki A et al (2003) Radial patterning of Arabidopsis shoots by class III HD-ZIP and KANADI genes. Curr Biol 13(20):1768–1774 (Epub 2003/10/17. PubMed PMID: 14561401)Fisher K, Turner S (2007) PXY, a receptor-like kinase essential for maintaining polarity during plant vascular-tissue development. Curr Biol 17(12):1061–1066. https://doi.org/10.1016/j.cub.2007.05.049Hirakawa Y, Shinohara H, Kondo Y, Inoue A, Nakanomyo I, Ogawa M et al (2008) Non-cell-autonomous control of vascular stem cell fate by a CLE peptide/receptor system. Proc Natl Acad Sci 105(39):15208–15213. https://doi.org/10.1073/pnas.0808444105Etchells JP, Provost CM, Mishra L, Turner SR (2013) WOX4 and WOX14 act downstream of the PXY receptor kinase to regulate plant vascular proliferation independently of any role in vascular organisation. Development 140(10):89. https://doi.org/10.1242/dev.091314Hirakawa Y, Kondo Y, Fukuda H (2010) TDIF peptide signaling regulates vascular stem cell proliferation via the WOX4 homeobox gene in arabidopsis. Plant Cell 22(8):2618–2629. https://doi.org/10.1105/tpc.110.076083Ito Y, Nakanomio I, Motose H, Iwamoto K, Sawa S, Dohmae N, Fukuda H (2006) Dodeca-CLE peptides as suppressors of plant stem cell differentiation. Science 313(5788):842–855. https://doi.org/10.1126/science.1128436Turner S, Sieburth LE (2003) Vascular patterning. Arabidopsis Book 2:e0073. https://doi.org/10.1199/tab.0073(Epub 2003/01/01. PubMed PMID: 22303224; PubMed Central PMCID: PMCPMC3243335)Courtois-Moreau CL, Pesquet E, Sjodin A, Muñiz L, Bollhoner B, Kaneda M, Samuels L, Jansson S, Tuominen H (2009) A unique program for cell death in xylem fibers of Populus stem. Plant J 58:260–274. https://doi.org/10.1111/j.1365-313X.2008.03777.xOhashi-Ito K, Oda Y, Fukuda H (2010) Arabidopsis VASCULAR-RELATED NAC-DOMAIN6 directly regulates the genes that govern programmed cell death and secondary wall formation during xylem differentiation. Plant Cell 22(10):3461–3473Ikematsu S, Tasaka M, Torii KU, Uchida N (2017) ERECTA-family receptor kinase genes redundantly prevent premature progression of secondary growth in the Arabidopsis hypocotyl. New Phytol 213:1697–1709Fischer U, Teichmann T (2017) The ERECTA and ERECTA-like genes control a developmental shift during xylem formation in Arabidopsis. New Phytol 213:1562–1563Felipo-Benavent A, Urbez C, Blanco-Tourinan N, Serrano-Mislata A, Baumberger N, Achard P et al (2018) Regulation of xylem fiber differentiation by gibberellins through DELLA-KNAT1 interaction. Development 145(23):89. https://doi.org/10.1242/dev.164962(Epub 2018/11/06. PubMed PMID: 30389856)Liebsch D, Sunaryo W, Holmlund M, Norberg M, Zhang J, Hall HC, Helizon H, Jin X, Helariutta Y, Nilsson O, Polle A, Fischer U (2014) Class I KNOX transcription factors promote differentiation of cambial derivatives into xylem fibers in the Arabidopsis hypocotyl. Development 141:4311–4319Milhinhos A, Vera-Sirera F, Blanco-Tourinan N, Mari-Carmona C, Carrio-Segui A, Forment J et al (2019) SOBIR1/EVR prevents precocious initiation of fiber differentiation during wood development through a mechanism involving BP and ERECTA. Proc Natl Acad Sci USA. https://doi.org/10.1073/pnas.1807863116(Epub 2019/08/25. PubMed PMID: 31444299)Mitsuda N, Iwase A, Yamamoto H, Yoshida M, Seki M, Shinozaki K, Ohme-Takagi M (2007) NAC transcription factors, NST1 and NST3, are key regulators of the formation of secondary walls in woody tissues of Arabidopsis. Plant Cell 19(1):270–280Zhong R, Demura T, Ye ZH (2006) SND1, a NAC domain transcription factor, is a key regulator of secondary wall synthesis in fibers of Arabidopsis. Plant Cell 18(11):3158–3170Siebers T, Catarino B, Agusti J (2017) Identification and expression analyses of new potential regulators of xylem development and cambium activity in cassava (Manihot esculenta). Planta 245(3):539–548. https://doi.org/10.1007/s00425-016-2623-2Taylor-Teeples M, Lin L, Lucas de M, Turco G, Toal TW, Gaudinier A et al (2015) An Arabidopsis gene regulatory network for secondary cell wall synthesis. Nature 517(7536):7571–7575. https://doi.org/10.1038/nature14099(Epub 2014/12/24. PubMed PMID: 25533953; PubMed Central PMCID: P

    A Clustered-Based Segmentation of Beer Consumers: From “Beer Lovers” to “Beer to Fuddle”

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    This version of the article has been accepted for publication, after peer review, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: https://doi.org/10.1108/BFJ-11-2017-0628[Abstract] Purpose: New trends are emerging in the brewery sector; but to date beer consumer segmentations are scarce. In this context, the present study addresses the following questions: “Are beer consumers monolithic or are there different segments in the beer market?; and: “What are the main characteristics of the beer consumer segments?”. The purpose of this research is to examine the potential beer consumer segments and to profile them regarding their consumption behaviour. Methodology: Data from a sample of 592 consumers was analysed through hierarchical cluster analysis; and the validity of the cluster solutions was then examined through a Manova analysis. Findings: A five-cluster solution emerged, revealing different beer consumption patterns and preferences. These segments are identified as “beer lovers”, “circumspect seniors”, “social drinkers”, “homelike women” and “beer to fuddle consumers”. Value: Our findings suggest that beer consumers cannot be seen as a homogenous consumer group; and managers and brewers could manage beer as five different products, instead of considering beer as a single item

    Pescoço (Colo). [Revisão Técnica]

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    Diminished Perisomatic GABAergic Terminals on Cortical Neurons Adjacent to Amyloid Plaques

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    One of the main pathological hallmarks of Alzheimer's disease (AD) is the accumulation of plaques in the cerebral cortex, which may appear either in the neuropil or in direct association with neuronal somata. Since different axonal systems innervate the dendritic (mostly glutamatergic) and perisomatic (mostly GABAergic) regions of neurons, the accumulation of plaques in the neuropil or associated with the soma might produce different alterations to synaptic circuits. We have used a variety of conventional light, confocal and electron microscopy techniques to study their relationship with neuronal somata in the cerebral cortex from AD patients and APP/PS1 transgenic mice. The main finding was that the membrane surfaces of neurons (mainly pyramidal cells) in contact with plaques lack GABAergic perisomatic synapses. Since these perisomatic synapses are thought to exert a strong influence on the output of pyramidal cells, their loss may lead to the hyperactivity of the neurons in contact with plaques. These results suggest that plaques modify circuits in a more selective manner than previously thought

    Diffusion-Weighted Magnetic Resonance Imaging in Peritoneal Carcinomatosis from Ovarian Cancer: Diagnostic performance in correlation with surgical findings.

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    Purpose Ovarian cancer (OC) is the commonest cause of death by gynaecological cancer in developed countries. Peritoneal carcinomatosis (PC) complete debulking without residual disease of >1 cm is the best prognostic predictor in advanced OC. PC is assessed with Computed tomography (CT). CT accuracy and cytoreduction success predictive ability are limited. PET/CT is not an imaging standard for PC. PC shows high signal foci in Diffusion-weighted magnetic resonance imaging (DWI MRI). We assessed the diagnostic performance (DP) and tumour burden correlation of Whole body DWI with background suppression MRI (WB-DWIBS/MRI) in PC of suspected OC using the Peritoneal Cancer Index (PCI), referring to cytoreduction surgery as the standard reference. Method Fifty patients with suspicion of disseminated OC underwent cytoreduction and WB-DWIBS/MRI. The PCI scores tumour burden (0–3) in 13 anatomical regions (global range of 0–39). Two radiologists (Rad1/Rad2) assessed the PCI preoperatively and with surgical findings. We evaluated regional and global DP, the interobserver agreement (Cohen´s kappa coefficient), statistical differences (McNemar test) and tumour burden (Pearson’s test). Results 72% (36/50) were epithelial OC and 78% (39/50) achieved complete cytoreduction. Global-PCI correlation was 0.762 (Rad1) with DP: Sensitivity 0.84, specificity 0.89, accuracy 0.89, and kappa 0.41. Average global-PCI was 7. The pelvis and right hypochondrium showed the highest positive rate and DP, while the intestinal regions presented the lowest. Previous studies reported higher sensitivity than CT or PET/CT, although only a few used the PCI. Conclusions WB-DWIBS/MRI is reliable to depict, quantify and to predict complete cytoreductive surgery in OC PC.pre-print2737 K

    Tempo de trânsito alimentar no trato digestivo de um teleósteo brasileiro, Prochilodus scrofa (Steindachner, 1881) com o uso da radiografia

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    O tempo de passagem de alimentos através do trato digestivo do peixe detritívoro de água doce Prochilodus scrofa foi determinado com o uso de técnicas radiográficas e de sulfato de bário como meio de contraste. Os peixes foram mantidos em tanques com temperatura constante de 23ºC e receberam via oral, através de um cateter, uma mistura de 2,5 partes de ração peletizada moída e 1 parte de suspensão oral do meio de contraste (Celobar). As radiografias foram obtidas em intervalos de 3 horas. Imediatamente após a introdução da mistura, visualizou-se o preenchimento gástrico pelo contraste. Foi observado um esfíncter existente entre os estômagos cárdico e pilórico. Após 3 horas, 80 por cento do intestino proximal estava repleto. Após 6 horas, o contraste atingiu as porções proximal, média e distal do intestino. Após 9 horas, 70 por cento do intestino distal estava repleto, e após 12 horas, havia a marcação do segmento do reto (25 por cento da porção distal do intestino).Food passage time through the digestive tract of a detritivorous freshwater fish (Prochilodus scrofa) was determinate by radiographic techniques using barium sulfate as a contrast medium. The fish were kept in tanks at a constant temperature of 23.5ºC and received by an oral catheter a mixture of 2.5 parts of ground ration and 1 part of oral suspension of contrast medium (Celobar). Radiographs were taken at intervals of 3 hours. Immediately after the introduction of the mixture the stomach was outlined by the contrast. A sphincter was observed between the cardiac and the muscular stomachs. After 3 hours, 80 per cent of the proximal intestine was filled. After 6 hours the contrast reached the proximal, medial and distal portions of the intestine. After 9 hours 70 per cent of the distal intestine was filled and after 12 hours, the rectum segment was still marked (25 per cent of the distal portion of the intestine)

    Microvascular anatomy of canines stomach and gastric injury caused by nonsteroidalanti-inflammatory drugs

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    Os Antiinflamatórios Não Esteróides (AINEs) inibem a síntese de prostaglandinas, com subseqüente diminuição da secreção de muco e bicarbonato pelo epitélio gástrico, redução da hidrofobicidade da camada epitelial, comprometimento da reposição celular, redução do fluxo sanguíneo e aumento da aderência de neutrófilos. Ao longo dos anos, notou-se que as lesões gástricas provocadas pelo uso de AINEs se localizam com maior freqüência nas regiões do antro pilórico e curvatura menor do estômago. A maior susceptibilidade destas regiões pode ser explicada por sua anatomia microvascular, a qual apresenta capilares estreitos, tortuosos e com menor diâmetro que em outras regiões do estômago; estes são mais separados entre si e há menos anastomoses entre os capilares ascendentes, tornando-os mais predispostos à trombose e conseqüente lesão gástrica.The nonsteroidal antiinflammatory drugs (NSAIs) inhibit the synthesis of prostaglandins, with subsequent reduction of mucus and bicarbonate secretion by the gastric epithelium, reduction of the hydrophobicity of the epithelial layer, impairment of cellular restitution, reduction of the blood flow and increase of neutrophils adhesive properties. It has been known that the gastric lesions secondary to NSAIDs use are more often located in the antral piloric and lesser curvature regions of the stomach. The higher susceptibility of these regions can be explained by their microvascular anatomy, which presents capillaries that are narrower and more contorted than those observed in other regions of the stomach; they also are more separated one from the other and they have fewer anastomosis between the ascending capillaries, becoming more predisposed to thrombosis, and consequently to gastric injury

    Transcriptional diversification and functional conservation between DELLA proteins in Arabidopsis

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    [EN] Plasticity and robustness of signaling pathways partly rely on genetic redundancy, although the precise mechanism that provides functional specificity to the different redundant elements in a given process is often unknown. In Arabidopsis, functional redundancy in gibberellin signaling has been largely attributed to the presence of five members of the DELLA family of transcriptional regulators. Here, we demonstrate that two evolutionarily and functionally divergent DELLA proteins, RGL2 and RGA, can perform exchangeable functions when they are expressed under control of the reciprocal promoter. Furthermore, both DELLA proteins display equivalent abilities to interact with PIF4 and with other bHLH transcription factors with a reported role in the control of cell growth and seed germination. Therefore, we propose that functional diversification of Arabidopsis DELLA proteins has largely relied on changes in their gene expression patterns rather than on their ability to interact with different regulatory partners, model also supported by a clustering analysis of DELLA transcript profiles over a range of organs and growth conditions that revealed specific patterns of expression for each of these genes.We deeply appreciate the help of Marta Trenor and Laura Garcia-Carcel in the initial stages of this work. We also thank Tai-ping Sun (Duke University) and the Arabidpsis Biological Resource Center for seeds, Marta Boter for the pGBKT7 and pGADT7 Gateway vectors, Santiago Elena (IBMCP, CSIC-UPV) for useful comments on the manuscript, and Francois Parcy (IRTSV, CNRS-CEA) for fruitful discussions and hosting MAB. Work in the authors' laboratories is funded by grants BIO2007-60923 and BIO2005-07284 from the Spanish Ministry of Science and Innovation. J.G.B. is the recipient of a CSIC I3P Fellowship and J.A.M. is the recipient of a Fellowship from the Fundacion "la Caixa.Gallego-Bartolome, J.; Minguet, E.; Marin, JA.; Prat, S.; Blazquez Rodriguez, MA.; Alabadí Diego, D. (2010). Transcriptional diversification and functional conservation between DELLA proteins in Arabidopsis. Molecular Biology and Evolution. 27(6):1247-1256. https://doi.org/10.1093/molbev/msq0121247125627
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