The border cells are a cluster of 6–8 cells that migrate in the ovariole of the fruit-fly Drosophila melanogaster, during the process of oogenesis. A fly ovary consists of a string of ovarioles or egg chambers arranged in an increasing order of maturity. Each egg chamber contains 16 central germline, nurse cells surrounded by a monolayer epithelium of nearly 1000 follicle cells. At stage 8 of oogenesis, these cells initiate invading the neighbouring nurse cells, and reach the oocyte boundary by Stage 10.

Mechanism of action

The border cells are specified by the activation of the JAK-STAT pathway in response to the cytokine, Unpaired. The signaling initiates by binding of Unpaired ligand to the Domeless receptor.[1] The migratory fate is acquired by the activation of slbo,[2] a transcription factor that leads to the transformation of stationary follicle cells into the migratory border cell fate by regulating the expression of various genes. Once the cluster detaches from the anterior end of the ovariole, a gradient of chemokines, PDGF and VEGF (PVF1) aids in the directional migration of border cells towards the oocyte.[3] The timing of the border cell migration along with egg chamber development is coordinated by ecdysone, a steroid hormone, which functions through Taiman, ecdysone receptor and ultraspiracle receptors.[4] These cells migrate as a free group by means of transient cell-cell adhesions, further initiating signaling cascades that regulate expression of cytoskeletal components and triggers cellular extensions enabling forward movement. The invasive movement of the cluster towards the posteriorly located oocyte is followed by the off-centred movement towards the dorsal side of the egg chamber. The second kind of movement is mediated by the binding of Gurken, Spitz and Keren ligands to the EGFR on the border cells.[5][6]

Significance

The directional and collective migration of border cells aids in the formation of micropyle, a specialised passage through which the sperm enters during fertilisation.[7] Studying cell migration is important from the point of view of metastasis, and for this reason, several model organisms are used to determine what molecules are important in initiating, maintaining and guiding moving cells. Drosophila melanogaster is one of the favorite organisms for studying biological phenomena. The border cells of the Drosophila ovary are a genetically tractable system for studying diverse aspects of migrating phenotype. After identifying the genes that are important for this phenotype, their homologs can be investigated for putative roles in turning non-invasive cancerous tumors into metastatic ones.[8]

References

  1. ↑ Ghiglione, Christian; Devergne, Olivier; Georgenthum, Emmanuelle; Carballès, Fabrice; Médioni, Caroline; Cerezo, Delphine; Noselli, Stéphane (2002-12-01). "The Drosophila cytokine receptor Domeless controls border cell migration and epithelial polarization during oogenesis". Development. 129 (23): 5437–5447. doi:10.1242/dev.00116. ISSN 1477-9129. PMID 12403714. S2CID 1613810.
  2. ↑ Montell, D. J.; Rorth, P.; Spradling, A. C. (1992-10-02). "slow border cells, a locus required for a developmentally regulated cell migration during oogenesis, encodes Drosophila C/EBP". Cell. 71 (1): 51–62. doi:10.1016/0092-8674(92)90265-e. ISSN 0092-8674. PMID 1394432. S2CID 22360057.
  3. ↑ Duchek, Peter; Somogyi, Kálmán; Jékely, Gáspár; Beccari, Simone; Rørth, Pernille (2001-10-05). "Guidance of Cell Migration by the Drosophila PDGF/VEGF Receptor". Cell. 107 (1): 17–26. doi:10.1016/S0092-8674(01)00502-5. ISSN 0092-8674. PMID 11595182. S2CID 16681564.
  4. ↑ Bai, Jianwu; Uehara, Yoshihiko; Montell, Denise J. (2000-12-22). "Regulation of Invasive Cell Behavior by Taiman, a Drosophila Protein Related to AIB1, a Steroid Receptor Coactivator Amplified in Breast Cancer". Cell. 103 (7): 1047–1058. doi:10.1016/S0092-8674(00)00208-7. ISSN 0092-8674. PMID 11163181. S2CID 13004669.
  5. ↑ McDonald, Jocelyn A.; Pinheiro, Elaine M.; Kadlec, Lisa; Schupbach, Trudi; Montell, Denise J. (2006-08-01). "Multiple EGFR ligands participate in guiding migrating border cells". Developmental Biology. 296 (1): 94–103. doi:10.1016/j.ydbio.2006.04.438. ISSN 0012-1606. PMID 16712835.
  6. ↑ Bianco, Ambra; Poukkula, Minna; Cliffe, Adam; Mathieu, Juliette; Luque, Carlos M.; Fulga, Tudor A.; Rørth, Pernille (July 2007). "Two distinct modes of guidance signalling during collective migration of border cells". Nature. 448 (7151): 362–365. Bibcode:2007Natur.448..362B. doi:10.1038/nature05965. ISSN 1476-4687. PMID 17637670. S2CID 4369682.
  7. ↑ Montell, D. J.; Rorth, P.; Spradling, A. C. (1992-10-02). "slow border cells, a locus required for a developmentally regulated cell migration during oogenesis, encodes Drosophila C/EBP". Cell. 71 (1): 51–62. doi:10.1016/0092-8674(92)90265-e. ISSN 0092-8674. PMID 1394432. S2CID 22360057.
  8. ↑ Cheung, Kevin J.; Ewald, Andrew J. (2016-04-08). "A collective route to metastasis: Seeding by tumor cell clusters". Science. 352 (6282): 167–169. Bibcode:2016Sci...352..167C. doi:10.1126/science.aaf6546. ISSN 1095-9203. PMC 8183671. PMID 27124449.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.