Literature DB >> 23274420

Expression of pluripotency factors in larval epithelia of the frog Xenopus: evidence for the presence of cornea epithelial stem cells.

Kimberly J Perry1, Alvin G Thomas, Jonathan J Henry.   

Abstract

Understanding the biology of somatic stem cells in self renewing tissues represents an exciting field of study, especially given the potential to harness these cells for tissue regeneration and repair in treating injury and disease. The mammalian cornea contains a population of basal epithelial stem cells involved in cornea homeostasis and repair. Research has been restricted to mammalian systems and little is known about the presence or function of these stem cells in other vertebrates. Therefore, we carried out studies to characterize frog cornea epithelium. Careful examination shows that the Xenopus larval cornea epithelium consists of three distinct layers that include an outer epithelial layer and underlying basal epithelium, in addition to a deeper fibrous layer that contains the main sensory nerve trunks that give rise to numerous branches that extend into these epithelia. These nerves convey sensory and presumably also autonomic innervation to those tissues. The sensory nerves are all derived as branches of the trigeminal nerve/ganglion similar to the situation encountered in mammals, though there appear to be some potentially interesting differences, which are detailed in this paper. We show further that numerous pluripotency genes are expressed by cells in the cornea epithelium, including: sox2, p63, various oct4 homologs, c-myc, klf4 and many others. Antibody localization revealed that p63, a well known mammalian epithelial stem cell marker, was localized strictly to all cells in the basal cornea epithelium. c-myc, was visualized in a smaller subset of basal epithelial cells and adjacent stromal tissue predominately at the periphery of the cornea (limbal zone). Finally, sox2 protein was found to be present throughout all cells of both the outer and basal epithelia, but was much more intensely expressed in a distinct subset of cells that appeared to be either multinucleate or possessed multi-lobed nuclei that are normally located at the periphery of the cornea. Using a thymidine analog (EdU), we were able to label mitotically active cells, which revealed that cell proliferation takes place throughout the cornea epithelium, predominantly in the basal epithelial layer. Species of Xenopus and one other amphibian are unique in their ability to replace a missing lens from cells derived from the basal cornea epithelium. Using EdU we show, as others have previously, that proliferating cells within the cornea epithelium do contribute to the formation of these regenerated lenses. Furthermore, using qPCR we determined that representatives of various pluripotency genes (i.e., sox2, p63 and oct60) are upregulated early during the process of lens regeneration. Antibody labeling showed that the number of sox2 expressing cells increased dramatically within 4 h following lens removal and these cells were scattered throughout the basal layer of the cornea epithelium. Historically, the process of lens regeneration in Xenopus had been described as one involving transdifferentiation of cornea epithelial cells (i.e., one involving cellular dedifferentiation followed by redifferentiation). Our combined observations provide evidence that a population of stem cells exists within the Xenopus cornea. We hypothesize that the basal epithelium contains oligopotent epithelial stem cells that also represent the source of regenerated lenses in the frog. Future studies will be required to clearly identify the source of these lenses.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23274420      PMCID: PMC3558918          DOI: 10.1016/j.ydbio.2012.12.005

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  68 in total

1.  PAX6 expression identifies progenitor cells for corneal keratocytes.

Authors:  Martha L Funderburgh; Yiqin Du; Mary M Mann; Nirmala SundarRaj; James L Funderburgh
Journal:  FASEB J       Date:  2005-05-18       Impact factor: 5.191

2.  Xenopus POU factors of subclass V inhibit activin/nodal signaling during gastrulation.

Authors:  Ying Cao; Doreen Siegel; Walter Knöchel
Journal:  Mech Dev       Date:  2006-06-14       Impact factor: 1.882

3.  Macrophage invasion and phagocytic activity during lens regeneration from the iris epithelium in newts.

Authors:  R W Reyer
Journal:  Am J Anat       Date:  1990-08

4.  Organization of corneal afferent axons in the trigeminal nerve root entry zone in the cat.

Authors:  C Morgan; P J Jannetta; W C deGroat
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

5.  Lens differentiation from the cornea following lens extirpation or cornea transplantation in Xenopus laevis.

Authors:  P R Waggoner
Journal:  J Exp Zool       Date:  1973-10

6.  Regional biosynthetic markers in the early amphibian embryo.

Authors:  J M Slack
Journal:  J Embryol Exp Morphol       Date:  1984-04

7.  alpha-, beta- and gamma-Crystallins in the regenerating lens of Notophthalmus viridescens.

Authors:  D S McDevitt; S K Brahma
Journal:  Exp Eye Res       Date:  1982-04       Impact factor: 3.467

8.  Characterization of Danio rerio Nanog and functional comparison to Xenopus Vents.

Authors:  Maximilian Schuff; Doreen Siegel; Melanie Philipp; Karin Bundschu; Nicole Heymann; Cornelia Donow; Walter Knöchel
Journal:  Stem Cells Dev       Date:  2011-10-03       Impact factor: 3.272

9.  Origins of the renal innervation in the primate, Macaca fascicularis.

Authors:  C F Marfurt; S F Echtenkamp; M A Jones
Journal:  J Auton Nerv Syst       Date:  1989-07

10.  Differentiation-related expression of a major 64K corneal keratin in vivo and in culture suggests limbal location of corneal epithelial stem cells.

Authors:  A Schermer; S Galvin; T T Sun
Journal:  J Cell Biol       Date:  1986-07       Impact factor: 10.539

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  14 in total

Review 1.  Diverse Evolutionary Origins and Mechanisms of Lens Regeneration.

Authors:  Jonathan J Henry; Paul W Hamilton
Journal:  Mol Biol Evol       Date:  2018-07-01       Impact factor: 16.240

Review 2.  Elixir of Life: Thwarting Aging With Regenerative Reprogramming.

Authors:  Ergin Beyret; Paloma Martinez Redondo; Aida Platero Luengo; Juan Carlos Izpisua Belmonte
Journal:  Circ Res       Date:  2018-01-05       Impact factor: 17.367

3.  Retinoic acid regulation by CYP26 in vertebrate lens regeneration.

Authors:  Alvin G Thomas; Jonathan J Henry
Journal:  Dev Biol       Date:  2013-12-30       Impact factor: 3.582

4.  Molecular markers for corneal epithelial cells in larval vs. adult Xenopus frogs.

Authors:  Surabhi Sonam; Jennifer A Srnak; Kimberly J Perry; Jonathan J Henry
Journal:  Exp Eye Res       Date:  2019-04-11       Impact factor: 3.467

5.  Expression of pluripotency factors in echinoderm regeneration.

Authors:  Vladimir S Mashanov; Olga R Zueva; José E García-Arrarás
Journal:  Cell Tissue Res       Date:  2014-12-03       Impact factor: 5.249

6.  The miRNA-34a/Sirt1/p53 pathway in a rat model of lens regeneration.

Authors:  Xue Bi; Rui Wang; Hui Song; Yuchuan Wang; Peng Hao; Xuan Li
Journal:  Ann Transl Med       Date:  2022-06

7.  Unique expression patterns of the embryonal stem cell marker SOX2 and hormone receptors suggest the existence of a subpopulation of epithelial stem/progenitor cells in porcine and bovine endometrium.

Authors:  Jiri Lenz; Petra Konecna; Frantisek Tichy; Dominika Machacova; Ludek Fiala; Pavel Hurnik; Michal Kyllar
Journal:  Vet Med Sci       Date:  2022-05-13

Review 8.  Cell signaling pathways in vertebrate lens regeneration.

Authors:  Jonathan J Henry; Alvin G Thomas; Paul W Hamilton; Lisa Moore; Kimberly J Perry
Journal:  Curr Top Microbiol Immunol       Date:  2013       Impact factor: 4.291

Review 9.  The lens regenerative competency of limbal vs. central regions of mature Xenopus cornea epithelium.

Authors:  Paul W Hamilton; Jonathan J Henry
Journal:  Exp Eye Res       Date:  2016-08-26       Impact factor: 3.467

10.  Lens regeneration from the cornea requires suppression of Wnt/β-catenin signaling.

Authors:  Paul W Hamilton; Yu Sun; Jonathan J Henry
Journal:  Exp Eye Res       Date:  2016-01-08       Impact factor: 3.467

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