Revisão Revisado por pares

Regeneration of the Lens in the Amphibian Eye

1954; University of Chicago Press; Volume: 29; Issue: 1 Linguagem: Inglês

10.1086/399936

ISSN

1539-7718

Autores

Randall W. Reyer,

Tópico(s)

Connexins and lens biology

Resumo

Previous articleNext article Regeneration of the Lens in the Amphibian EyeRandall W. ReyerRandall W. ReyerPDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmailPrint SectionsMoreDetailsFiguresReferencesCited by The Quarterly Review of Biology Volume 29, Number 1Mar., 1954 Published in association with Stony Brook University Article DOIhttps://doi.org/10.1086/399936 Views: 10Total views on this site Citations: 170Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Georgios Tsissios, Gabriella Theodoroudis-Rapp, Weihao Chen, Anthony Sallese, Byran Smucker, Lake Ernst, Junfan Chen, Yiqi Xu, Sophia Ratvasky, Hui Wang, Katia Del Rio-Tsonis Characterizing the lens regeneration process in Pleurodeles waltl, Differentiation 145 (Mar 2023).https://doi.org/10.1016/j.diff.2023.02.003Sangwon Min, Jessica L. Whited Limb blastema formation: How much do we know at a genetic and epigenetic level?, Journal of Biological Chemistry 299, no.22 (Feb 2023): 102858.https://doi.org/10.1016/j.jbc.2022.102858Georgios Tsissios, Anthony Sallese, Weihao Chen, Alyssa Miller, Hui Wang, Katia Del Rio-Tsonis In Vivo and Ex Vivo View of Newt Lens Regeneration, (Oct 2022): 197–208.https://doi.org/10.1007/978-1-0716-2659-7_13Tatiana Solovieva Development of the smooth newt, Lissotriton vulgaris , as observed in a garden pond during lockdown, Developmental Dynamics 251, no.66 (Aug 2021): 1077–1087.https://doi.org/10.1002/dvdy.405Eleonora N. Grigoryan Pigment Epithelia of the Eye: Cell-Type Conversion in Regeneration and Disease, Life 12, no.33 (Mar 2022): 382.https://doi.org/10.3390/life12030382Vivien Bothe, Kristin Mahlow, Nadia B. Fröbisch A histological study of normal and pathological limb regeneration in the Mexican axolotl Ambystoma mexicanum, Journal of Experimental Zoology Part B: Molecular and Developmental Evolution 336, no.22 (May 2020): 116–128.https://doi.org/10.1002/jez.b.22950Paul Palmquist-Gomes, José María Pérez-Pomares, Juan Antonio Guadix Cell-based therapies for the treatment of myocardial infarction: lessons from cardiac regeneration and repair mechanisms in non-human vertebrates, Heart Failure Reviews 24, no.11 (Nov 2018): 133–142.https://doi.org/10.1007/s10741-018-9750-8Jonathan J Henry, Paul W Hamilton, Bing Su Diverse Evolutionary Origins and Mechanisms of Lens Regeneration, Molecular Biology and Evolution 35, no.77 (Mar 2018): 1563–1575.https://doi.org/10.1093/molbev/msy045Detlev Arendt, Jacob M. Musser, Clare V. H. Baker, Aviv Bergman, Connie Cepko, Douglas H. Erwin, Mihaela Pavlicev, Gerhard Schlosser, Stefanie Widder, Manfred D. Laubichler, Günter P. Wagner The origin and evolution of cell types, Nature Reviews Genetics 17, no.1212 (Nov 2016): 744–757.https://doi.org/10.1038/nrg.2016.127Mark Naguib, Liam Reid Amphibians: biology and captive care, Companion Animal 20, no.1212 (Dec 2015): 694–701.https://doi.org/10.12968/coan.2015.20.12.694Qiao Li, Hao Yang, Tao P. Zhong Regeneration across Metazoan Phylogeny: Lessons from Model Organisms, Journal of Genetics and Genomics 42, no.22 (Feb 2015): 57–70.https://doi.org/10.1016/j.jgg.2014.12.002Joshua Mutua, Yuka Jinno, Souhei Sakata, Yoshifumi Okochi, Shuichi Ueno, Hidekazu Tsutsui, Takafumi Kawai, Yasuhiro Iwao, Yasushi Okamura Functional diversity of voltage-sensing phosphatases in two urodele amphibians, Physiological Reports 2, no.77 (Jul 2014): e12061.https://doi.org/10.14814/phy2.12061Sarah Wassmer, Margaret Beddaoui, Payman Rajai, Réjean Munger, Catherine Tsilfidis, Panagiotis A. Tsonis A Focus on the Optical Properties of the Regenerated Newt Lens, PLoS ONE 8, no.88 (Aug 2013): e70845.https://doi.org/10.1371/journal.pone.0070845Constance Cepko, Donna M. Fekete Sensory Epithelium of the Eye and Ear, (Jan 2013): 739–751.https://doi.org/10.1016/B978-0-12-385942-6.00063-9Kiyokazu Agata, Takeshi Inoue Survey of the differences between regenerative and non-regenerative animals, Development, Growth & Differentiation 54, no.22 (Feb 2012): 143–152.https://doi.org/10.1111/j.1440-169X.2011.01323.xTomonori Katsuyama, Renato Paro Epigenetic reprogramming during tissue regeneration, FEBS Letters 585, no.1111 (May 2011): 1617–1624.https://doi.org/10.1016/j.febslet.2011.05.010Yongjun Wang, Ruili Wang, Shengjuan Jiang, Weijuan Zhou, Yan Liu, Yingjie Wang, Qing Gu, Yun Gu, Yingying Dong, Mei Liu, Xingxing Gu, Fei Ding, Xiaosong Gu, Cheng-Xin Gong Gecko CD59 Is Implicated in Proximodistal Identity during Tail Regeneration, PLoS ONE 6, no.33 (Mar 2011): e17878.https://doi.org/10.1371/journal.pone.0017878Erica L. Malloch, Kimberly J. Perry, Lisa Fukui, Verity R. Johnson, Jason Wever, Caroline W. Beck, Michael W. King, Jonathan J. Henry Gene expression profiles of lens regeneration and development in Xenopus laevis, Developmental Dynamics 238, no.99 (Aug 2009): 2340–2356.https://doi.org/10.1002/dvdy.21998Sergio Filoni Retina and lens regeneration in anuran amphibians, Seminars in Cell & Developmental Biology 20, no.55 (Jul 2009): 528–534.https://doi.org/10.1016/j.semcdb.2008.11.015Alan Colman, Oliver Dreesen Induced pluripotent stem cells and the stability of the differentiated state, EMBO reports 10, no.77 (Jun 2009): 714–721.https://doi.org/10.1038/embor.2009.142Toshinori Hayashi, Nobuhiko Mizuno, Hisato Kondoh Determinative roles of FGF and Wnt signals in iris‐derived lens regeneration in newt eye, Development, Growth & Differentiation 50, no.44 (Mar 2008): 279–287.https://doi.org/10.1111/j.1440-169X.2008.01005.xJonathan J. Henry, Jason M. Wever, M. Natalia Vergara, Lisa Fukui Xenopus, an Ideal Vertebrate System for Studies of Eye Development and Regeneration, (Jan 2008): 57–92.https://doi.org/10.1016/B978-0-12-374169-1.00006-0Kannan Krishnan, Thandavarayan Kathiresan, Rajeev Raman, Bheemreddy Rajini, Vishnu M. Dhople, Ramesh K. Aggrawal, Yogendra Sharma Ubiquitous Lens α-, β-, and γ-Crystallins Accumulate in Anuran Cornea as Corneal Crystallins, Journal of Biological Chemistry 282, no.2626 (Jun 2007): 18953–18959.https://doi.org/10.1074/jbc.M609275200 References, (Jan 2007): 325–369.https://doi.org/10.1016/B978-012369439-3/50018-0Toshinori Hayashi, Nobuhiko Mizuno, Ritsuko Takada, Shinji Takada, Hisato Kondoh Determinative role of Wnt signals in dorsal iris-derived lens regeneration in newt eye, Mechanisms of Development 123, no.1111 (Nov 2006): 793–800.https://doi.org/10.1016/j.mod.2006.08.009James W. Godwin, Jeremy P. 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Tsonis Eye on regeneration, The Anatomical Record Part B: The New Anatomist 287B, no.11 (Nov 2005): 42–48.https://doi.org/10.1002/ar.b.20084Nobuhiko Mizuno, Yoko Ueda, Hisato Kondoh Requirement for βB1‐crystallin promoter of Xenopus laevis in embryonic lens development and lens regeneration, Development, Growth & Differentiation 47, no.33 (Apr 2005): 131–140.https://doi.org/10.1111/j.1440-169X.2005.00789.xFrank J. Lovicu, Michael L. Robinson Development of the Ocular Lens, 84 (Jan 2010).https://doi.org/10.1017/CBO9780511529825Toshinori Hayashi, Nobuhiko Mizuno, Yoko Ueda, Mitsumasa Okamoto, Hisato Kondoh FGF2 triggers iris-derived lens regeneration in newt eye, Mechanisms of Development 121, no.66 (Jun 2004): 519–526.https://doi.org/10.1016/j.mod.2004.04.010J. P. Brockes, P. Martin, Yutaka Imokawa, András Simon, Jeremy P. Brockes A critical role for thrombin in vertebrate lens regeneration, Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 359, no.14451445 (May 2004): 765–776.https://doi.org/10.1098/rstb.2004.1467Constance Cepko, Donna M. Fekete Sensory Epithelium of the Eye and Ear, (Jan 2004): 253–263.https://doi.org/10.1016/B978-012436643-5/50031-6T Okamoto, T Kanao, Y Miyachi, N Nohara Marked increase in the rate of ocular lens regeneration in the newt, Cynops pyrrhogaster , following partial body exposure to low dose X-rays, The British Journal of Radiology 77, no.913913 (Jan 2004): 49–51.https://doi.org/10.1259/bjr/22916297Yutaka Imokawa, Jeremy P Brockes Selective Activation of Thrombin Is a Critical Determinant for Vertebrate Lens Regeneration, Current Biology 13, no.1010 (May 2003): 877–881.https://doi.org/10.1016/S0960-9822(03)00294-XJeremy P. 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Okada Lens regeneration in Xenopus is not a mere repeat of lens development, with respect to crystallin gene expression, Differentiation 64, no.33 (Mar 1999): 143–149.https://doi.org/10.1046/j.1432-0436.1999.6430143.xJAE CHANG JUNG, KATIA DEL RIO-TSONIS, PANAGIOTIS A. TSONIS Regulation of Homeobox-containing Genes during Lens Regeneration, Experimental Eye Research 66, no.33 (Mar 1998): 361–370.https://doi.org/10.1006/exer.1997.0437J Brockes Regeneration and cancer, Biochimica et Biophysica Acta (BBA) - Reviews on Cancer 1377, no.11 (Feb 1998): M1–M11.https://doi.org/10.1016/S0304-419X(97)00029-2Jeremy P. Brockes Amphibian Limb Regeneration: Rebuilding a Complex Structure, Science 276, no.53095309 (Apr 1997): 81–87.https://doi.org/10.1126/science.276.5309.81David S. McDevitt, Samir K. Brahma, Yves Courtois, Jean-Claude Jeanny Fibroblast growth factor receptors and regeneration of the eye lens, Developmental Dynamics 208, no.22 (Feb 1997): 220–226.https://doi.org/10.1002/(SICI)1097-0177(199702)208:2 3.0.CO;2-KRyosuke Makita, Hisato Kondoh, Mitsumasa Okamoto Transgenesis of newt with exogenous gene expression facilitated by satellite 2 repeats, Development, Growth & Differentiation 37, no.55 (Oct 2003): 605–616.https://doi.org/10.1046/j.1440-169X.1995.00016.xGoro Eguchi Chapter 9 Lens transdifferentiation in the vertebrate retinal pigmented epithelial cell, Progress in Retinal Research 12 (Jan 1993): 205–230.https://doi.org/10.1016/0278-4327(93)90010-QJoséR. Ortiz, Marc Vigny, Yves Courtois, Jean-Claude Jeanny Immunocytochemical study of extracellular matrix components during lens and neural retina regeneration in the adult newt, Experimental Eye Research 54, no.66 (Jun 1992): 861–870.https://doi.org/10.1016/0014-4835(92)90149-MRandall W. Reyer Macrophage invasion and phagocytic activity during lens regeneration from the iris epithelium in newts, American Journal of Anatomy 188, no.44 (Feb 2005): 329–344.https://doi.org/10.1002/aja.1001880402Randall W. Reyer Macrophage mobilization and morphology during lens regeneration from the iris epithelium in newts: Studies with correlated scanning and transmission electron microscopy, American Journal of Anatomy 188, no.44 (Feb 2005): 345–365.https://doi.org/10.1002/aja.1001880403Margaret S. Saha, Clayton L. Spann, Robert M. Grainger Embryonic lens induction: more than meets the optic vesicle, Cell Differentiation and Development 28, no.33 (Dec 1989): 153–171.https://doi.org/10.1016/0922-3371(89)90001-4Gordana Jurić-Lekić, Anton Švajger Lentoid formation in ectopic grafts of lentectomized eyes of rat foetuses, Cell Differentiation and Development 27, no.33 (Sep 1989): 225–231.https://doi.org/10.1016/0922-3371(89)90702-8Steven A. 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Reyer Availability time of tritium‐labeled DNA Precursors in newt eyes following intraperitoneal injection of 3 H‐thymidine, Journal of Experimental Zoology 226, no.11 (Jun 2005): 101–121.https://doi.org/10.1002/jez.1402260113Olga G. Stroeva, Victor I. Mitashov Retinal Pigment Epithelium: Proliferation and Differentiation during Development and Regeneration, (Jan 1983): 221–293.https://doi.org/10.1016/S0074-7696(08)61689-7C. A. Berardi, D. S. McDevitt Lens regeneration from the dorsal iris inEurycea bislineata, the two-lined salamander, Experientia 38, no.77 (Jul 1982): 851–852.https://doi.org/10.1007/BF01972311Frank Chan Comparison of lens regeneration in adult newts,Triturus viridescens, between light and dark preadapted and non-preadapted animals, The Anatomical Record 202, no.44 (Apr 1982): 521–525.https://doi.org/10.1002/ar.1092020411Randall W. 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