#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Multiplexin Promotes Heart but Not Aorta Morphogenesis by Polarized Enhancement of Slit/Robo Activity at the Heart Lumen


The Drosophila heart tube represents a structure that similarly to vertebrates' primary heart tube exhibits a large lumen; the mechanisms promoting heart tube morphology in both Drosophila and vertebrates are poorly understood. We identified Multiplexin (Mp), the Drosophila orthologue of mammalian Collagen-XV/XVIII, and the only structural heart-specific protein described so far in Drosophila, as necessary and sufficient for shaping the heart tube lumen, but not that of the aorta. Mp is expressed specifically at the stage of heart tube closure, in a polarized fashion, uniquely along the cardioblasts luminal membrane, and its absence results in an extremely small heart tube lumen. Importantly, Mp forms a protein complex with Slit, and interacts genetically with both slit and robo in the formation of the heart tube. Overexpression of Mp in cardioblasts promotes a large heart lumen in a Slit-dependent manner. Moreover, Mp alters Slit distribution, and promotes the formation of multiple Slit endocytic vesicles, similarly to the effect of overexpression of Robo in these cells. Our data are consistent with Mp-dependent enhancement of Slit/Robo activity and signaling, presumably by affecting Slit protein stabilization, specifically at the lumen side of the heart tube. This activity results with a Slit-dependent, local reduction of F-actin levels at the heart luminal membrane, necessary for forming the large heart tube lumen. Consequently, lack of Mp results in decreased diastolic capacity, leading to reduced heart contractility, as measured in live fly hearts. In summary, these findings show that the polarized localization of Mp controls the direction, timing, and presumably the extent of Slit/Robo activity and signaling at the luminal membrane of the heart cardioblasts. This regulation is essential for the morphogenetic changes that sculpt the heart tube in Drosophila, and possibly in forming the vertebrates primary heart tube.


Vyšlo v časopise: Multiplexin Promotes Heart but Not Aorta Morphogenesis by Polarized Enhancement of Slit/Robo Activity at the Heart Lumen. PLoS Genet 9(6): e32767. doi:10.1371/journal.pgen.1003597
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003597

Souhrn

The Drosophila heart tube represents a structure that similarly to vertebrates' primary heart tube exhibits a large lumen; the mechanisms promoting heart tube morphology in both Drosophila and vertebrates are poorly understood. We identified Multiplexin (Mp), the Drosophila orthologue of mammalian Collagen-XV/XVIII, and the only structural heart-specific protein described so far in Drosophila, as necessary and sufficient for shaping the heart tube lumen, but not that of the aorta. Mp is expressed specifically at the stage of heart tube closure, in a polarized fashion, uniquely along the cardioblasts luminal membrane, and its absence results in an extremely small heart tube lumen. Importantly, Mp forms a protein complex with Slit, and interacts genetically with both slit and robo in the formation of the heart tube. Overexpression of Mp in cardioblasts promotes a large heart lumen in a Slit-dependent manner. Moreover, Mp alters Slit distribution, and promotes the formation of multiple Slit endocytic vesicles, similarly to the effect of overexpression of Robo in these cells. Our data are consistent with Mp-dependent enhancement of Slit/Robo activity and signaling, presumably by affecting Slit protein stabilization, specifically at the lumen side of the heart tube. This activity results with a Slit-dependent, local reduction of F-actin levels at the heart luminal membrane, necessary for forming the large heart tube lumen. Consequently, lack of Mp results in decreased diastolic capacity, leading to reduced heart contractility, as measured in live fly hearts. In summary, these findings show that the polarized localization of Mp controls the direction, timing, and presumably the extent of Slit/Robo activity and signaling at the luminal membrane of the heart cardioblasts. This regulation is essential for the morphogenetic changes that sculpt the heart tube in Drosophila, and possibly in forming the vertebrates primary heart tube.


Zdroje

1. ZaffranS, FraschM (2002) Early signals in cardiac development. Circ Res 91: 457–469.

2. OlsonEN (2006) Gene regulatory networks in the evolution and development of the heart. Science 313: 1922–1927.

3. BierE, BodmerR (2004) Drosophila, an emerging model for cardiac disease. Gene 342: 1–11.

4. TaoY, SchulzRA (2007) Heart development in Drosophila. Semin Cell Dev Biol 18: 3–15.

5. HaagTA, HaagNP, LekvenAC, HartensteinV (1999) The role of cell adhesion molecules in Drosophila heart morphogenesis: faint sausage, shotgun/DE-cadherin, and laminin A are required for discrete stages in heart development. Dev Biol 208: 56–69.

6. YarnitzkyT, VolkT (1995) Laminin is required for heart, somatic muscles, and gut development in the Drosophila embryo. Dev Biol 169: 609–618.

7. VanderploegJ, Vazquez PazLL, MacMullinA, JacobsJR (2012) Integrins are required for cardioblast polarisation in Drosophila. BMC Dev Biol 12: 8.

8. MacMullinA, JacobsJR (2006) Slit coordinates cardiac morphogenesis in Drosophila. Dev Biol 293: 154–164.

9. MedioniC, AstierM, ZmojdzianM, JaglaK, SemerivaM (2008) Genetic control of cell morphogenesis during Drosophila melanogaster cardiac tube formation. J Cell Biol 182: 249–261.

10. Santiago-MartinezE, SoplopNH, PatelR, KramerSG (2008) Repulsion by Slit and Roundabout prevents Shotgun/E-cadherin-mediated cell adhesion during Drosophila heart tube lumen formation. J Cell Biol 182: 241–248.

11. QianL, LiuJ, BodmerR (2005) Slit and Robo control cardiac cell polarity and morphogenesis. Curr Biol 15: 2271–2278.

12. AlbrechtS, AltenheinB, PaululatA (2011) The transmembrane receptor Uncoordinated5 (Unc5) is essential for heart lumen formation in Drosophila melanogaster. Dev Biol 350: 89–100.

13. MeyerF, MoussianB (2009) Drosophila multiplexin (Dmp) modulates motor axon pathfinding accuracy. Dev Growth Differ 51: 483–498.

14. MomotaR, NaitoI, NinomiyaY, OhtsukaA (2011) Drosophila type XV/XVIII collagen, Mp, is involved in Wingless distribution. Matrix Biol 30: 258–266.

15. MuonaA, EklundL, VaisanenT, PihlajaniemiT (2002) Developmentally regulated expression of type XV collagen correlates with abnormalities in Col15a1(−/−) mice. Matrix Biol 21: 89–102.

16. RasiK, PiuholaJ, CzabankaM, SormunenR, IlvesM, et al. (2010) Collagen XV is necessary for modeling of the extracellular matrix and its deficiency predisposes to cardiomyopathy. Circ Res 107: 1241–1252.

17. EklundL, PiuholaJ, KomulainenJ, SormunenR, OngvarrasoponeC, et al. (2001) Lack of type XV collagen causes a skeletal myopathy and cardiovascular defects in mice. Proc Natl Acad Sci U S A 98: 1194–1199.

18. MedioniC, BertrandN, MesbahK, HudryB, DupaysL, et al. (2010) Expression of Slit and Robo genes in the developing mouse heart. Dev Dyn 239: 3303–3311.

19. MommersteegMT, AndrewsWD, YpsilantiAR, ZelinaP, YehML, et al. (2013) Slit-roundabout signaling regulates the development of the cardiac systemic venous return and pericardium. Circ Res 112: 465–475.

20. RothbergJM, HartleyDA, WaltherZ, Artavanis-TsakonasS (1988) slit: an EGF-homologous locus of D. melanogaster involved in the development of the embryonic central nervous system. Cell 55: 1047–1059.

21. SpitzweckB, BrankatschkM, DicksonBJ (2010) Distinct protein domains and expression patterns confer divergent axon guidance functions for Drosophila Robo receptors. Cell 140: 409–420.

22. EvansTA, BashawGJ (2010) Functional diversity of Robo receptor immunoglobulin domains promotes distinct axon guidance decisions. Curr Biol 20: 567–572.

23. ReuvenyA, ElhananyH, VolkT (2009) Enhanced sensitivity of midline glial cells to apoptosis is achieved by HOW(L)-dependent repression of Diap1. Mech Dev 126: 30–41.

24. YangL, BashawGJ (2006) Son of sevenless directly links the Robo receptor to rac activation to control axon repulsion at the midline. Neuron 52: 595–607.

25. HsounaA, KimYS, VanBerkumMF (2003) Abelson tyrosine kinase is required to transduce midline repulsive cues. J Neurobiol 57: 15–30.

26. HsounaA, VanBerkumMF (2008) Abelson tyrosine kinase and Calmodulin interact synergistically to transduce midline guidance cues in the Drosophila embryonic CNS. Int J Dev Neurosci 26: 345–354.

27. OcorrK, ReevesNL, WessellsRJ, FinkM, ChenHS, et al. (2007) KCNQ potassium channel mutations cause cardiac arrhythmias in Drosophila that mimic the effects of aging. Proc Natl Acad Sci U S A 104: 3943–3948.

28. ChananaB, SteigemannP, JackleH, VorbruggenG (2009) Reception of Slit requires only the chondroitin-sulphate-modified extracellular domain of Syndecan at the target cell surface. Proc Natl Acad Sci U S A 106: 11984–11988.

29. KnoxJ, MoyerK, YacoubN, SoldaatC, KomosaM, et al. (2011) Syndecan contributes to heart cell specification and lumen formation during Drosophila cardiogenesis. Dev Biol 356 (2): 279–90.

30. Rodriguez-FraticelliAE, AuzanM, AlonsoMA, BornensM, Martin-BelmonteF (2012) Cell confinement controls centrosome positioning and lumen initiation during epithelial morphogenesis. J Cell Biol 198: 1011–1023.

31. RheeJ, BuchanT, ZukerbergL, LilienJ, BalsamoJ (2007) Cables links Robo-bound Abl kinase to N-cadherin-bound beta-catenin to mediate Slit-induced modulation of adhesion and transcription. Nat Cell Biol 9: 883–892.

32. HanaiJ, GloyJ, KarumanchiSA, KaleS, TangJ, et al. (2002) Endostatin is a potential inhibitor of Wnt signaling. J Cell Biol 158: 529–539.

33. Passos-BuenoMR, SuzukiOT, Armelin-CorreaLM, SertieAL, ErreraFI, et al. (2006) Mutations in collagen 18A1 and their relevance to the human phenotype. An Acad Bras Cienc 78: 123–131.

34. FukaiN, EklundL, MarnerosAG, OhSP, KeeneDR, et al. (2002) Lack of collagen XVIII/endostatin results in eye abnormalities. Embo J 21: 1535–1544.

35. WangX, HarrisRE, BaystonLJ, AsheHL (2008) Type IV collagens regulate BMP signalling in Drosophila. Nature 455: 72–77.

36. BuntS, HooleyC, HuN, ScahillC, WeaversH, et al. (2010) Hemocyte-secreted type IV collagen enhances BMP signaling to guide renal tubule morphogenesis in Drosophila. Dev Cell 19: 296–306.

37. DengWM, SchneiderM, FrockR, Castillejo-LopezC, GamanEA, et al. (2003) Dystroglycan is required for polarizing the epithelial cells and the oocyte in Drosophila. Development 130: 173–184.

38. HarpazN, VolkT (2011) A novel method for obtaining semi-thin cross sections of the Drosophila heart and their labeling with multiple antibodies. Methods 56: 63–68.

39. GilsohnE, VolkT (2010) Slowdown promotes muscle integrity by modulating integrin-mediated adhesion at the myotendinous junction. Development 137: 785–794.

40. OcorrK, FinkM, CammaratoA, BernsteinS, BodmerR (2009) Semi-automated Optical Heartbeat Analysis of small hearts. J Vis Exp

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2013 Číslo 6
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#