JNK signaling controls border cell cluster integrity and collective cell migration

被引:91
作者
Llense, Flora [1 ]
Martin-Blanco, Enrique [1 ]
机构
[1] CSIC, Inst Biol Mol Barcelona, E-08028 Barcelona, Spain
关键词
D O I
10.1016/j.cub.2008.03.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Collective cell movement is a mechanism for invasion identified in many developmental events. Examples include the movement of lateral-line neurons in Zebrafish, cells in the inner blastocyst, and metastasis of epithelial tumors [1]. One key model to study collective migration is the movement of border cell clusters in Drosophila. Drosophila egg chambers contain 15 nurse cells and a single oocyte surrounded by somatic follicle cells. At their anterior end, polar cells recruit several neighboring follicle cells to form the border cell cluster [2]. By stage 9, and over 6 hr, border cells migrate as a cohort between nurse cells toward the oocyte. The specification and directionality of border cell movement are regulated by hormonal and signaling mechanisms [3]. However, how border cells are held together while they migrate is not known. Here, we show that a negative-feedback loop controlling JNK activity regulates border cell cluster integrity. JNK signaling modulates contacts between border cells and between border cells and substratum to sustain collective migration by regulating several effectors including the polarity factor Bazooka and the cytoskeletal adaptor D-Paxillin. We anticipate a role for the JNK pathway in controlling collective cell movements in other morphogenetic and clinical models.
引用
收藏
页码:538 / 544
页数:7
相关论文
共 32 条
[11]   Tumour-cell invasion and migration: Diversity and escape mechanisms [J].
Friedl, P ;
Wolf, K .
NATURE REVIEWS CANCER, 2003, 3 (05) :362-374
[12]   Myosin VI is required for E-cadherin-mediated border cell migration [J].
Geisbrecht, ER ;
Montell, DJ .
NATURE CELL BIOLOGY, 2002, 4 (08) :616-620
[13]  
Grammon M, 2002, DEVELOPMENT, V129, P5131
[14]   JNK phosphorylates paxillin and regulates cell migration [J].
Huang, C ;
Rajfur, Z ;
Borchers, C ;
Schaller, MD ;
Jacobson, K .
NATURE, 2003, 424 (6945) :219-223
[15]   Signal transduction by the c-Jun N-terminal kinase (JNK) - from inflammation to development [J].
Ip, YT ;
Davis, RJ .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (02) :205-219
[16]  
Jackson SM, 2002, DEVELOPMENT, V129, P4423
[17]   Rho GTPases: Biochemistry and biology [J].
Jaffe, AB ;
Hall, A .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2005, 21 :247-269
[18]   Flytrap, a database documenting a GFP protein-trap insertion screen in Drosophila melanogaster [J].
Kelso, RJ ;
Buszczak, M ;
Quiñones, AT ;
Castiblanco, C ;
Mazzalupo, S ;
Cooley, L .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D418-D420
[19]   Control of epithelial cell shape and polarity [J].
Knust, E .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2000, 10 (05) :471-475
[20]   LOCALIZATION AND FUNCTIONS OF PROTEIN-KINASE-A DURING DROSOPHILA OOGENESIS [J].
LANE, ME ;
KALDERON, D .
MECHANISMS OF DEVELOPMENT, 1995, 49 (03) :191-200