#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Multiple Wnts Redundantly Control Polarity Orientation in Epithelial Stem Cells


During development, cell polarization is often coordinated to harmonize tissue patterning and morphogenesis. However, how extrinsic signals synchronize cell polarization is not understood. In Caenorhabditis elegans, most mitotic cells are polarized along the anterior-posterior axis and divide asymmetrically. Although this process is regulated by a Wnt-signaling pathway, Wnts functioning in cell polarity have been demonstrated in only a few cells. We analyzed how Wnts control cell polarity, using compound Wnt mutants, including animals with mutations in all five Wnt genes. We found that somatic gonadal precursor cells (SGPs) are properly polarized and oriented in quintuple Wnt mutants, suggesting Wnts are dispensable for the SGPs' polarity, which instead requires signals from the germ cells. Thus, signals from the germ cells organize the C. elegans somatic gonad. In contrast, in compound but not single Wnt mutants, most of the six seam cells, V1–V6 (which are epithelial stem cells), retain their polarization, but their polar orientation becomes random, indicating that it is redundantly regulated by multiple Wnt genes. In contrast, in animals in which the functions of three Wnt receptors (LIN-17, MOM-5, and CAM-1) are disrupted—the stem cells are not polarized and divide symmetrically—suggesting that the Wnt receptors are essential for generating polarity and that they function even in the absence of Wnts. All the seam cells except V5 were polarized properly by a single Wnt gene expressed at the cell's anterior or posterior. The ectopic expression of posteriorly expressed Wnts in an anterior region and vice versa rescued polarity defects in compound Wnt mutants, raising two possibilities: one, Wnts permissively control the orientation of polarity; or two, Wnt functions are instructive, but which orientation they specify is determined by the cells that express them. Our results provide a paradigm for understanding how cell polarity is coordinated by extrinsic signals.


Vyšlo v časopise: Multiple Wnts Redundantly Control Polarity Orientation in Epithelial Stem Cells. PLoS Genet 7(10): e32767. doi:10.1371/journal.pgen.1002308
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002308

Souhrn

During development, cell polarization is often coordinated to harmonize tissue patterning and morphogenesis. However, how extrinsic signals synchronize cell polarization is not understood. In Caenorhabditis elegans, most mitotic cells are polarized along the anterior-posterior axis and divide asymmetrically. Although this process is regulated by a Wnt-signaling pathway, Wnts functioning in cell polarity have been demonstrated in only a few cells. We analyzed how Wnts control cell polarity, using compound Wnt mutants, including animals with mutations in all five Wnt genes. We found that somatic gonadal precursor cells (SGPs) are properly polarized and oriented in quintuple Wnt mutants, suggesting Wnts are dispensable for the SGPs' polarity, which instead requires signals from the germ cells. Thus, signals from the germ cells organize the C. elegans somatic gonad. In contrast, in compound but not single Wnt mutants, most of the six seam cells, V1–V6 (which are epithelial stem cells), retain their polarization, but their polar orientation becomes random, indicating that it is redundantly regulated by multiple Wnt genes. In contrast, in animals in which the functions of three Wnt receptors (LIN-17, MOM-5, and CAM-1) are disrupted—the stem cells are not polarized and divide symmetrically—suggesting that the Wnt receptors are essential for generating polarity and that they function even in the absence of Wnts. All the seam cells except V5 were polarized properly by a single Wnt gene expressed at the cell's anterior or posterior. The ectopic expression of posteriorly expressed Wnts in an anterior region and vice versa rescued polarity defects in compound Wnt mutants, raising two possibilities: one, Wnts permissively control the orientation of polarity; or two, Wnt functions are instructive, but which orientation they specify is determined by the cells that express them. Our results provide a paradigm for understanding how cell polarity is coordinated by extrinsic signals.


Zdroje

1. LawrencePAStruhlGCasalJ 2007 Planar cell polarity: one or two pathways? Nature reviews Genetics 8 555 563

2. KellyMChenP 2007 Shaping the mammalian auditory sensory organ by the planar cell polarity pathway. The International journal of developmental biology 51 535 547

3. McNeillH 2010 Planar cell polarity: keeping hairs straight is not so simple. Cold Spring Harbor perspectives in biology 2 a003376

4. SimonsMMlodzikM 2008 Planar cell polarity signaling: from fly development to human disease. Annual review of genetics 42 517 540

5. AxelrodJD 2009 Progress and challenges in understanding planar cell polarity signaling. Seminars in cell & developmental biology 20 964 971

6. DabdoubADonohueMJBrennanAWolfVMontcouquiolM 2003 Wnt signaling mediates reorientation of outer hair cell stereociliary bundles in the mammalian cochlea. Development 130 2375 2384

7. RohdeLAHeisenbergCP 2007 Zebrafish gastrulation: cell movements, signals, and mechanisms. International review of cytology 261 159 192

8. RoszkoISawadaASolnica-KrezelL 2009 Regulation of convergence and extension movements during vertebrate gastrulation by the Wnt/PCP pathway. Seminars in cell & developmental biology 20 986 997

9. MizumotoKSawaH 2007 Two betas or not two betas: regulation of asymmetric division by beta-catenin. Trends Cell Biol 17 465 473

10. MizumotoKSawaH 2007 Cortical beta-catenin and APC regulate asymmetric nuclear beta-catenin localization during asymmetric cell division in C. elegans. Dev Cell 12 287 299

11. GoldsteinBTakeshitaHMizumotoKSawaH 2006 Wnt signals can function as positional cues in establishing cell polarity. Dev Cell 10 391 396

12. GreenJLInoueTSternbergPW 2008 Opposing Wnt pathways orient cell polarity during organogenesis. Cell 134 646 656

13. SulstonJEHorvitzHR 1977 Post-embryonic cell lineages of the nematode, Caenorhabditis elegans. Developmental Biology 56 110 156

14. TakeshitaHSawaH 2005 Asymmetric cortical and nuclear localizations of WRM-1/b-catenin during asymmetric cell division in C. elegans. Genes Dev 19 1743 1748

15. GleasonJEEisenmannDM 2010 Wnt signaling controls the stem cell-like asymmetric division of the epithelial seam cells during C. elegans larval development. Developmental biology 348 58 66

16. WhangboJHarrisJKenyonC 2000 Multiple levels of regulation specify the polarity of an asymmetric cell division in C. elegans. Development 127 4587 4598

17. GilleardJSShafiYBarryJDMcGheeJD 1999 ELT-3: A Caenorhabditis elegans GATA factor expressed in the embryonic epidermis during morphogenesis. Developmental biology 208 265 280

18. KohKRothmanJH 2001 ELT-5 and ELT-6 are required continuously to regulate epidermal seam cell differentiation and cell fusion in C. elegans. Development 128 2867 2880

19. GleasonJESzyleykoEAEisenmannDM 2006 Multiple redundant Wnt signaling components function in two processes during C. elegans vulval development. Dev Biol 298 442 457

20. NakamuraKKimSIshidateTBeiYPangK 2005 Wnt signaling drives WRM-1/beta-catenin asymmetries in early C. elegans embryos. Genes Dev 19 1749 1754

21. WaringDAWrischnikLKenyonC 1992 Cell signals allow the expression of a pre-existent neural pattern in C. elegans. Development 116 457 466

22. GreenJLKuntzSGSternbergPW 2008 Ror receptor tyrosine kinases: orphans no more. Trends Cell Biol 18 536 544

23. ForresterWCDellMPerensEGarrigaG 1999 A C. elegans Ror receptor tyrosine kinase regulates cell motility and asymmetric cell division. Nature 400 881 885

24. SawaHLobelLHorvitzHR 1996 The Caenorhabditis elegans gene lin-17, which is required for certain asymmetric cell divisions, encodes a putative seven-transmembrane protein similar to the Drosophila frizzled protein. Genes Dev 10 2189 2197

25. SongSZhangBSunHLiXXiangY 2010 A Wnt-Frz/Ror-Dsh pathway regulates neurite outgrowth in Caenorhabditis elegans. PLoS Genet 6 e1001056 doi:10.1371/journal.pgen.1001056

26. KennerdellJRFetterRDBargmannCI 2009 Wnt-Ror signaling to SIA and SIB neurons directs anterior axon guidance and nerve ring placement in C. elegans. Development 136 3801 3810

27. HermanMAVassilievaLLHorvitzHRShawJEHermanRK 1995 The C. elegans gene lin-44, which controls the polarity of certain asymmetric cell divisions, encodes a Wnt protein and acts cell nonautonomously. Cell 83 101 110

28. PanCLHowellJEClarkSGHilliardMCordesS 2006 Multiple Wnts and frizzled receptors regulate anteriorly directed cell and growth cone migrations in Caenorhabditis elegans. Dev Cell 10 367 377

29. WhangboJKenyonC 1999 A Wnt signaling system that specifies two patterns of cell migration in C. elegans. Mol Cell 4 851 858

30. CoudreuseDYRoelGBetistMCDestreeOKorswagenHC 2006 Wnt gradient formation requires retromer function in Wnt-producing cells. Science 312 921 924

31. HarfeBDVaz GomesAKenyonCLiuJKrauseM 1998 Analysis of a Caenorhabditis elegans Twist homolog identifies conserved and divergent aspects of mesodermal patterning. Genes & development 12 2623 2635

32. OkkemaPGHaEHaunCChenWFireA 1997 The Caenorhabditis elegans NK-2 homeobox gene ceh-22 activates pharyngeal muscle gene expression in combination with pha-1 and is required for normal pharyngeal development. Development 124 3965 3973

33. OkkemaPGFireA 1994 The Caenorhabditis elegans NK-2 class homeoprotein CEH-22 is involved in combinatorial activation of gene expression in pharyngeal muscle. Development 120 2175 2186

34. KimbleJHirshD 1979 The postembryonic cell lineages of the hermaphrodite and male gonads in Caenorhabditis elegans. Developmental biology 70 396 417

35. SiegfriedKRKimbleJ 2002 POP-1 controls axis formation during early gonadogenesis in C. elegans. Development 129 443 453

36. StromeSMartinPSchierenbergEPaulsenJ 1995 Transformation of the germ line into muscle in mes-1 mutant embryos of C. elegans. Development 121 2961 2972

37. LoganCYNusseR 2004 The Wnt Signaling Pathway in Development and Disease. Annu Rev Cell Dev Biol 20 781 810

38. IkeyaMLeeSMJohnsonJEMcMahonAPTakadaS 1997 Wnt signalling required for expansion of neural crest and CNS progenitors. Nature 389 966 970

39. WildwaterMSanderNde VreedeGvan den HeuvelS 2011 Cell Shape and Wnt Signaling Redundantly Control the Division Axis of C. elegans Epithelial Stem Cells. Development In press

40. SilhankovaMKorswagenHC 2007 Migration of neuronal cells along the anterior-posterior body axis of C. elegans: Wnts are in control. Current opinion in genetics & development 17 320 325

41. BrennerS 1974 The genetics of Caenorhabditis elegans. Genetics 77 71 94

42. HermanMAHorvitzHR 1994 The Caenorhabditis elegans gene lin-44 controls the polarity of asymmetric cell divisions. Development 120 1035 1047

43. ZinovyevaAYForresterWC 2005 The C. elegans Frizzled CFZ-2 is required for cell migration and interacts with multiple Wnt signaling pathways. Dev Biol 285 447 461

44. MaloofJNWhangboJHarrisJMJongewardGDKenyonC 1999 A Wnt signaling pathway controls hox gene expression and neuroblast migration in C. elegans. Development 126 37 49

45. SugiokaKSawaH 2010 Regulation of asymmetric positioning of nuclei by Wnt and Src signaling and its roles in POP-1/TCF nuclear asymmetry in Caenorhabditis elegans. Genes to cells : devoted to molecular & cellular mechanisms 15 397 407

46. RocheleauCEDownsWDLinRWittmannCBeiY 1997 Wnt signaling and an APC-related gene specify endoderm in early C. elegans embryos. Cell 90 707 716

47. InoueTOzHSWilandDGharibSDeshpandeR 2004 C. elegans LIN-18 is a Ryk ortholog and functions in parallel to LIN-17/Frizzled in Wnt signaling. Cell 118 795 806

48. CapowskiEEMartinPGarvinCStromeS 1991 Identification of grandchildless loci whose products are required for normal germ-line development in the nematode Caenorhabditis elegans. Genetics 129 1061 1072

49. HoffmannMSegbertCHelbigGBossingerO 2010 Intestinal tube formation in Caenorhabditis elegans requires vang-1 and egl-15 signaling. Developmental biology 339 268 279

50. WrischnikLAKenyonCJ 1997 The role of lin-22, a hairy/enhancer of split homolog, in patterning the peripheral nervous system of C. elegans. Development 124 2875 2888

51. ZhongWFengHSantiagoFEKipreosET 2003 CUL-4 ubiquitin ligase maintains genome stability by restraining DNA-replication licensing. Nature 423 885 889

52. LiuZFujiiTNukazukaAKurokawaRSuzukiM 2005 C. elegans PlexinA PLX-1 mediates a cell contact-dependent stop signal in vulval precursor cells. Developmental biology 282 138 151

53. SiegfriedKRKiddAR3rdChesneyMAKimbleJ 2004 The sys-1 and sys-3 genes cooperate with Wnt signaling to establish the proximal-distal axis of the Caenorhabditis elegans gonad. Genetics 166 171 186

54. MelloCCKramerJMStinchcombDAmbrosV 1991 Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences. EMBO J 10 3959 3970

55. LaiCCHongKKinnellMChalfieMDriscollM 1996 Sequence and transmembrane topology of MEC-4, an ion channel subunit required for mechanotransduction in Caenorhabditis elegans. The Journal of cell biology 133 1071 1081

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2011 Číslo 10
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#