Polarized actin and VE-cadherin dynamics regulate junctional remodelling and cell migration during sprouting angiogenesis

. 2017 Dec 20 ; 8 (1) : 2210. [epub] 20171220

Jazyk angličtina Země Velká Británie, Anglie Médium electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid29263363
Odkazy

PubMed 29263363
PubMed Central PMC5738342
DOI 10.1038/s41467-017-02373-8
PII: 10.1038/s41467-017-02373-8
Knihovny.cz E-zdroje

VEGFR-2/Notch signalling regulates angiogenesis in part by driving the remodelling of endothelial cell junctions and by inducing cell migration. Here, we show that VEGF-induced polarized cell elongation increases cell perimeter and decreases the relative VE-cadherin concentration at junctions, triggering polarized formation of actin-driven junction-associated intermittent lamellipodia (JAIL) under control of the WASP/WAVE/ARP2/3 complex. JAIL allow formation of new VE-cadherin adhesion sites that are critical for cell migration and monolayer integrity. Whereas at the leading edge of the cell, large JAIL drive cell migration with supportive contraction, lateral junctions show small JAIL that allow relative cell movement. VEGFR-2 activation initiates cell elongation through dephosphorylation of junctional myosin light chain II, which leads to a local loss of tension to induce JAIL-mediated junctional remodelling. These events require both microtubules and polarized Rac activity. Together, we propose a model where polarized JAIL formation drives directed cell migration and junctional remodelling during sprouting angiogenesis.

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Gerhardt H, et al. VEGF guides angiogenic sprouting utilizing endothelial tip cell filopodia. J. Cell. Biol. 2003;161:1163–1177. doi: 10.1083/jcb.200302047. PubMed DOI PMC

Jakobsson L, et al. Endothelial cells dynamically compete for the tip cell position during angiogenic sprouting. Nat. Cell. Biol. 2010;12:943–953. doi: 10.1038/ncb2103. PubMed DOI

Gaengel K, et al. The sphingosine-1-phosphate receptor S1PR1 restricts sprouting angiogenesis by regulating the interplay between VE-cadherin and VEGFR2. Dev. Cell. 2012;23:587–599. doi: 10.1016/j.devcel.2012.08.005. PubMed DOI

Bentley K, et al. The role of differential VE-cadherin dynamics in cell rearrangement during angiogenesis. Nat. Cell Biol. 2014;16:309–321. doi: 10.1038/ncb2926. PubMed DOI

Yamamoto H, et al. Integrin beta1 controls VE-cadherin localization and blood vessel stability. Nat. Commun. 2015;6:6429. doi: 10.1038/ncomms7429. PubMed DOI

Abraham S, et al. VE-Cadherin-mediated cell-cell interaction suppresses sprouting via signaling to MLC2 phosphorylation. Curr. Biol. 2009;19:668–674. doi: 10.1016/j.cub.2009.02.057. PubMed DOI

Carmeliet P, et al. Targeted deficiency or cytosolic truncation of the VE-cadherin gene in mice impairs VEGF-mediated endothelial survival and angiogenesis. Cell. 1999;98:147–157. doi: 10.1016/S0092-8674(00)81010-7. PubMed DOI

Abu Taha A, Taha M, Seebach J, Schnittler HJ. ARP2/3-mediated junction-associated lamellipodia control VE-cadherin-based cell junction dynamics and maintain monolayer integrity. Mol. Biol. Cell. 2014;25:245–256. doi: 10.1091/mbc.E13-07-0404. PubMed DOI PMC

Rajput C, et al. Neural Wiskott-Aldrich syndrome protein (N-WASP)-mediated p120-catenin interaction with Arp2-Actin complex stabilizes endothelial adherens junctions. J. Biol. Chem. 2013;288:4241–4250. doi: 10.1074/jbc.M112.440396. PubMed DOI PMC

Krause M, Gautreau A. Steering cell migration: lamellipodium dynamics and the regulation of directional persistence. Nat. Rev. Mol. Cell. Biol. 2014;15:577–590. doi: 10.1038/nrm3861. PubMed DOI

Breslin JW, Zhang XE, Worthylake RA, Souza-Smith FM. Involvement of local lamellipodia in endothelial barrier function. PLoS ONE. 2015;10:e0117970. doi: 10.1371/journal.pone.0117970. PubMed DOI PMC

Seebach J, et al. The CellBorderTracker, a novel tool to quantitatively analyze spatiotemporal endothelial junction dynamics at the subcellular level. Histochem. Cell. Biol. 2015;144:517–532. doi: 10.1007/s00418-015-1357-8. PubMed DOI

Abella JV, et al. Isoform diversity in the Arp2/3 complex determines actin filament dynamics. Nat. Cell Biol. 2016;18:76–86. doi: 10.1038/ncb3286. PubMed DOI

Hall A. Rho GTPases and the control of cell behaviour. Biochem. Soc. Trans. 2005;33:891–895. doi: 10.1042/BST0330891. PubMed DOI

Hayer A, et al. Engulfed cadherin fingers are polarized junctional structures between collectively migrating endothelial cells. Nat. Cell. Biol. 2016;18:1311–1323. doi: 10.1038/ncb3438. PubMed DOI PMC

Millan J, et al. Adherens junctions connect stress fibres between adjacent endothelial cells. BMC Biol. 2010;8:11. doi: 10.1186/1741-7007-8-11. PubMed DOI PMC

Fraccaroli A, et al. Visualization of endothelial actin cytoskeleton in the mouse retina. PLoS. One. 2012;7:e47488. doi: 10.1371/journal.pone.0047488. PubMed DOI PMC

Gelfand MV, et al. Neuropilin-1 functions as a VEGFR2 co-receptor to guide developmental angiogenesis independent of ligand binding. Elife. 2014;3:e03720. doi: 10.7554/eLife.03720. PubMed DOI PMC

Shen Q, Rigor RR, Pivetti CD, Wu MH, Yuan SY. Myosin light chain kinase in microvascular endothelial barrier function. Cardiovasc. Res. 2010;87:272–280. doi: 10.1093/cvr/cvq144. PubMed DOI PMC

Schnittler HJ, Wilke A, Gress T, Suttorp N, Drenckhahn D. Role of actin and myosin in the control of paracellular permeability in pig, rat and human vascular endothelium. J. Physiol. 1990;431:379–401. doi: 10.1113/jphysiol.1990.sp018335. PubMed DOI PMC

Li Z, et al. Regulation of PTEN by Rho small GTPases. Nat. Cell. Biol. 2005;7:399–404. doi: 10.1038/ncb1236. PubMed DOI

Riento K, Ridley AJ. Rocks: multifunctional kinases in cell behaviour. Nat. Rev. Mol. Cell. Biol. 2003;4:446–456. doi: 10.1038/nrm1128. PubMed DOI

Etienne-Manneville S. Microtubules in cell migration. Annu. Rev. Cell. Dev. Biol. 2013;29:471–499. doi: 10.1146/annurev-cellbio-101011-155711. PubMed DOI

Mayor R, Etienne-Manneville S. The front and rear of collective cell migration. Nat. Rev. Mol. Cell. Biol. 2016;17:97–109. doi: 10.1038/nrm.2015.14. PubMed DOI

McCue S, et al. Shear stress regulates forward and reverse planar cell polarity of vascular endothelium in vivo and in vitro. Circ. Res. 2006;98:939–946. doi: 10.1161/01.RES.0000216595.15868.55. PubMed DOI

Drenckhahn D, Wagner J. Stress fibers in the splenic sinus endothelium in situ: molecular structure, relationship to the extracellular matrix, and contractility. J. Cell. Biol. 1986;102:1738–1747. doi: 10.1083/jcb.102.5.1738. PubMed DOI PMC

Garrett TA, Van Buul JD, Burridge K. VEGF-induced Rac1 activation in endothelial cells is regulated by the guanine nucleotide exchange factor Vav2. Exp. Cell. Res. 2007;313:3285–3297. doi: 10.1016/j.yexcr.2007.05.027. PubMed DOI PMC

Zeng H, Zhao D, Mukhopadhyay D. Flt-1-mediated downregulation of endothelial cell proliferation through pertussis toxin-sensitive G proteins, beta gamma subunits, small GTPase CDC42, and partly by Rac-1. J. Biol. Chem. 2002;277:4003–4009. doi: 10.1074/jbc.M110842200. PubMed DOI

Tarbashevich K, Reichman-Fried M, Grimaldi C, Raz E. Chemokine-Dependent pH elevation at the cell front sustains polarity in directionally migrating zebrafish germ cells. Curr. Biol. 2015;25:1096–1103. doi: 10.1016/j.cub.2015.02.071. PubMed DOI

Kardash E, et al. A role for Rho GTPases and cell-cell adhesion in single-cell motility in vivo. Nat. Cell. Biol. 2010;12:47–53. doi: 10.1038/ncb2003. PubMed DOI

Nakatsu, M. N., Davis, J. & Hughes, C. C. Optimized fibrin gel bead assay for the study of angiogenesis. J. Vis. Exp. 186 (2007). PubMed PMC

Nehls V, Drenckhahn D. A microcarrier-based cocultivation system for the investigation of factors and cells involved in angiogenesis in three-dimensional fibrin matrices in vitro. Histochem. Cell. Biol. 1995;104:459–466. doi: 10.1007/BF01464336. PubMed DOI

Phng LK, Stanchi F, Gerhardt H. Filopodia are dispensable for endothelial tip cell guidance. Development. 2013;140:4031–4040. doi: 10.1242/dev.097352. PubMed DOI

Pelham RJ, Chang F. Actin dynamics in the contractile ring during cytokinesis in fission yeast. Nature. 2002;419:82–86. doi: 10.1038/nature00999. PubMed DOI

Blanco R, Gerhardt H. VEGF and Notch in tip and stalk cell selection. Cold Spring Harb. Perspect. Med. 2013;3:a006569. doi: 10.1101/cshperspect.a006569. PubMed DOI PMC

De Smet F, Segura I, De Bock K, Hohensinner PJ, Carmeliet P. Mechanisms of vessel branching: filopodia on endothelial tip cells lead the way. Arterioscler. Thromb. Vasc. Biol. 2009;29:639–649. doi: 10.1161/ATVBAHA.109.185165. PubMed DOI

Hellstrom M, et al. Dll4 signalling through Notch1 regulates formation of tip cells during angiogenesis. Nature. 2007;445:776–780. doi: 10.1038/nature05571. PubMed DOI

Ehling M, Adams S, Benedito R, Adams RH. Notch controls retinal blood vessel maturation and quiescence. Development. 2013;140:3051–3061. doi: 10.1242/dev.093351. PubMed DOI

Sauteur L, et al. Cdh5/VE-cadherin promotes endothelial cell interface elongation via cortical actin polymerization during angiogenic sprouting. Cell Rep. 2014;9:504–513. doi: 10.1016/j.celrep.2014.09.024. PubMed DOI

Lampugnani MG, et al. The molecular organization of endothelial cell to cell junctions: differential association of plakoglobin, beta-catenin, and alpha- catenin with vascular endothelial cadherin (VE-cadherin) J. Cell. Biol. 1995;129:203–217. doi: 10.1083/jcb.129.1.203. PubMed DOI PMC

Benedito R, et al. Notch-dependent VEGFR3 upregulation allows angiogenesis without VEGF-VEGFR2 signalling. Nature. 2012;484:110–114. doi: 10.1038/nature10908. PubMed DOI

Tsuji-Tamura K, Ogawa M. Inhibition of the PI3K-Akt and mTORC1 signaling pathways promotes the elongation of vascular endothelial cells. J. Cell. Sci. 2016;129:1165–1178. doi: 10.1242/jcs.178434. PubMed DOI

Seebach J, et al. Regulation of endothelial barrier function during flow-induced conversion to an arterial phenotype. Cardiovasc. Res. 2007;75:596–607. doi: 10.1016/j.cardiores.2007.04.017. PubMed DOI

Wang Y, et al. Moesin1 and Ve-cadherin are required in endothelial cells during in vivo tubulogenesis. Development. 2010;137:3119–3128. doi: 10.1242/dev.048785. PubMed DOI PMC

Sugden WW, et al. Endoglin controls blood vessel diameter through endothelial cell shape changes in response to haemodynamic cues. Nat. Cell. Biol. 2017;19:653–665. doi: 10.1038/ncb3528. PubMed DOI PMC

Hasan SS, et al. Endothelial Notch signalling limits angiogenesis via control of artery formation. Nat. Cell. Biol. 2017;19:928–940. doi: 10.1038/ncb3574. PubMed DOI PMC

Lee CC, et al. Disrupting the CXCL12/CXCR4 axis disturbs the characteristics of glioblastoma stem-like cells of rat RG2 glioblastoma. Cancer Cell. Int. 2013;13:85. doi: 10.1186/1475-2867-13-85. PubMed DOI PMC

Gebala V, Collins R, Geudens I, Phng LK, Gerhardt H. Blood flow drives lumen formation by inverse membrane blebbing during angiogenesis in vivo. Nat. Cell Biol. 2016;18:443–450. doi: 10.1038/ncb3320. PubMed DOI PMC

Kametani Y, Takeichi M. Basal-to-apical cadherin flow at cell junctions. Nat. Cell Biol. 2007;9:92–U118. doi: 10.1038/ncb1520. PubMed DOI

Levayer R, Lecuit T. Oscillation and polarity of E-cadherin asymmetries control actomyosin flow patterns during morphogenesis. Dev. Cell. 2013;26:162–175. doi: 10.1016/j.devcel.2013.06.020. PubMed DOI

Kage F, et al. FMNL formins boost lamellipodial force generation. Nat. Commun. 2017;8:14832. doi: 10.1038/ncomms14832. PubMed DOI PMC

Bentley K, Mariggi G, Gerhardt H, Bates PA. Tipping the balance: robustness of tip cell selection, migration and fusion in angiogenesis. PLoS Comput. Biol. 2009;5:e1000549. doi: 10.1371/journal.pcbi.1000549. PubMed DOI PMC

Nakayama M, et al. Spatial regulation of VEGF receptor endocytosis in angiogenesis. Nat. Cell Biol. 2013;15:249–260. doi: 10.1038/ncb2679. PubMed DOI PMC

Gavard J, Gutkind JS. VEGF controls endothelial-cell permeability by promoting the beta-arrestin-dependent endocytosis of VE-cadherin. Nat. Cell Biol. 2006;8:1223–1234. doi: 10.1038/ncb1486. PubMed DOI

Wright TJ, Leach L, Shaw PE, Jones P. Dynamics of vascular endothelial-cadherin and beta-catenin localization by vascular endothelial growth factor-induced angiogenesis in human umbilical vein cells. Exp. Cell. Res. 2002;280:159–168. doi: 10.1006/excr.2002.5636. PubMed DOI

Luxton GW, Gundersen GG. Orientation and function of the nuclear-centrosomal axis during cell migration. Curr. Opin. Cell. Biol. 2011;23:579–588. doi: 10.1016/j.ceb.2011.08.001. PubMed DOI PMC

Waterman-Storer CM, Worthylake RA, Liu BP, Burridge K, Salmon ED. Microtubule growth activates Rac1 to promote lamellipodial protrusion in fibroblasts. Nat. Cell Biol. 1999;1:45–50. doi: 10.1038/9018. PubMed DOI

Fraccaroli A, et al. Endothelial alpha-parvin controls integrity of developing vasculature and is required for maintenance of cell-cell junctions. Circ. Res. 2015;117:29–40. doi: 10.1161/CIRCRESAHA.117.305818. PubMed DOI PMC

Nohata N, et al. Temporal-specific roles of Rac1 during vascular development and retinal angiogenesis. Dev. Biol. 2016;411:183–194. doi: 10.1016/j.ydbio.2016.02.005. PubMed DOI

Hoelzle MK, Svitkina T. The cytoskeletal mechanisms of cell-cell junction formation in endothelial cells. Mol. Biol. Cell. 2012;23:310–323. doi: 10.1091/mbc.E11-08-0719. PubMed DOI PMC

Kronstein R, et al. Caveolin-1 opens endothelial cell junctions by targeting catenins. Cardiovasc. Res. 2012;93:130–140. doi: 10.1093/cvr/cvr256. PubMed DOI

Ballestrem C, Wehrle-Haller B, Hinz B, Imhof BA. Actin-dependent lamellipodia formation and microtubule-dependent tail retraction control-directed cell migration. Mol. Biol. Cell. 2000;11:2999–3012. doi: 10.1091/mbc.11.9.2999. PubMed DOI PMC

Wojciak-Stothard B, Ridley AJ. Shear stress-induced endothelial cell polarization is mediated by Rho and Rac but not Cdc42 or PI 3-kinases. J. Cell Biol. 2003;161:429–439. doi: 10.1083/jcb.200210135. PubMed DOI PMC

Dieckmann-Schuppert A, Schnittler HJ. A simple assay for quantification of protein in tissue sections, cell cultures, and cell homogenates, and of protein immobilized on solid surfaces. Cell Tissue Res. 1997;288:119–126. doi: 10.1007/s004410050799. PubMed DOI

Claxton S, et al. Efficient, inducible Cre-recombinase activation in vascular endothelium. Genesis. 2008;46:74–80. doi: 10.1002/dvg.20367. PubMed DOI

Koch U, et al. Delta-like 4 is the essential, nonredundant ligand for Notch1 during thymic T cell lineage commitment. J. Exp. Med. 2008;205:2515–2523. doi: 10.1084/jem.20080829. PubMed DOI PMC

Kohli, P., Kumar, P. & Torr, P. P3 and Beyond: Solving Energies with Higher Order Cliques. IEEE Computer Society Conference on Computer Vision and Pattern Recognition (CVPR) 1–8 (IEEE, Los Alamitos, USA, 2007).

Zhang, J., Djolonga, J. & Krause, A. International Conference on Computer Vision (ICCV, Los Alamitos, USA, 2015).

Sixta, T. & Flach, B. 19th International Conference on Medical Image Computing and Computer Assisted Intervention (Springer International Publishing AG, Cham, Switzerland, 2016).

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