Literature DB >> 26432953

Bilateral retinal microglial response to unilateral optic nerve transection in rats.

L P Cen1, M Han1, L Zhou1, L Tan1, J J Liang1, C P Pang2, M Zhang3.   

Abstract

When retinal ganglion cells undergo apoptosis after optic nerve (ON) injury, microglial cells proliferate and promptly clear the degenerated debris in the ipsilateral retina. However, microglial changes in the contralateral retina have not been fully elucidated. This study characterized the long-term bilateral retinal microglial responses after unilateral ON transection. We analyzed the time course of proliferation and morphology changes of microglial cells, between 3 days and 12 weeks post ON transection, of undisturbed and reactive microglia in bilateral retinas of adult Fischer rats with unilateral ON transection. Microglia in retinas without ON transection were distributed homogeneously and possessed a highly ramified morphology, as judged by immunohistochemistry for ionized calcium-binding adapter molecule 1 (Iba1). After ON transection, microglia density in the ipsilateral retina increased gradually from 3 days to 2 weeks, and decreased from 3 weeks to 12 weeks, along with dramatic inverted alteration of process branch points of microglia in the ganglion cell layer (GCL). Transformation of ramified microglia into ameboid-like macrophages with few branching processes was observed in the ipsilateral retina from 1 week to 3 weeks. Though an increase in microglial density was weak in the contralateral retina and could only be statistically detected in the central retina, the morphological alteration over time was obvious and similar to that of the ipsilateral retina. In the inner plexiform layer (IPL), cell density and morphological changes of microglia in both the ipsilateral and contralateral retina were not prominent. These findings indicates that, though proliferation of microglial cells is weak in the contralateral retina after unilateral ON transection, conspicuous alterations in microglial morphology occur bilaterally. These suggest that using the contralateral retina as a control in studies of retinal degeneration should be considered with caution.
Copyright © 2015 IBRO. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  bilateral; microglia; optic nerve transection; retina

Mesh:

Substances:

Year:  2015        PMID: 26432953     DOI: 10.1016/j.neuroscience.2015.09.067

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  10 in total

1.  Mobile zinc increases rapidly in the retina after optic nerve injury and regulates ganglion cell survival and optic nerve regeneration.

Authors:  Yiqing Li; Lukas Andereggen; Kenya Yuki; Kumiko Omura; Yuqin Yin; Hui-Ya Gilbert; Burcu Erdogan; Maria S Asdourian; Christine Shrock; Silmara de Lima; Ulf-Peter Apfel; Yehong Zhuo; Michal Hershfinkel; Stephen J Lippard; Paul A Rosenberg; Larry Benowitz
Journal:  Proc Natl Acad Sci U S A       Date:  2017-01-03       Impact factor: 11.205

2.  A new fate mapping system reveals context-dependent random or clonal expansion of microglia.

Authors:  Tuan Leng Tay; Dominic Mai; Jana Dautzenberg; Francisco Fernández-Klett; Gen Lin; Moumita Datta; Anne Drougard; Thomas Stempfl; Alberto Ardura-Fabregat; Ori Staszewski; Anca Margineanu; Anje Sporbert; Lars M Steinmetz; J Andrew Pospisilik; Steffen Jung; Josef Priller; Dominic Grün; Olaf Ronneberger; Marco Prinz
Journal:  Nat Neurosci       Date:  2017-04-17       Impact factor: 24.884

3.  Response of the Retinal Nerve Fiber Layer Reflectance and Thickness to Optic Nerve Crush.

Authors:  Xiang-Run Huang; Wei Kong; Jianzhong Qiao
Journal:  Invest Ophthalmol Vis Sci       Date:  2018-04-01       Impact factor: 4.799

4.  Carbon monoxide treatment reduces microglial activation in the ischemic rat retina.

Authors:  Felix Ulbrich; Ulrich Goebel; Daniel Böhringer; Petar Charalambous; Wolf Alexander Lagrèze; Julia Biermann
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2016-07-21       Impact factor: 3.117

5.  Effect of Qingguang'an II on expressions of OX42 protein and IL-1β mRNA of retinal microglia cells of rats with chronic high intraocular pressure.

Authors:  Ya-Sha Zhou; Jian Xu; Jun Peng; Yue Liu; Gen-Yan Qin; Yi-Jing Yang; Qing-Hua Peng; Han-Yu Tan
Journal:  Int J Ophthalmol       Date:  2018-02-18       Impact factor: 1.779

6.  Microglial dynamics after axotomy-induced retinal ganglion cell death.

Authors:  Francisco M Nadal-Nicolás; Manuel Jiménez-López; Manuel Salinas-Navarro; Paloma Sobrado-Calvo; Manuel Vidal-Sanz; Marta Agudo-Barriuso
Journal:  J Neuroinflammation       Date:  2017-11-09       Impact factor: 8.322

Review 7.  Neuroinflammation as Fuel for Axonal Regeneration in the Injured Vertebrate Central Nervous System.

Authors:  Ilse Bollaerts; Jessie Van Houcke; Lien Andries; Lies De Groef; Lieve Moons
Journal:  Mediators Inflamm       Date:  2017-01-19       Impact factor: 4.711

8.  Neuronal Death in the Contralateral Un-Injured Retina after Unilateral Axotomy: Role of Microglial Cells.

Authors:  Fernando Lucas-Ruiz; Caridad Galindo-Romero; Kristy T Rodríguez-Ramírez; Manuel Vidal-Sanz; Marta Agudo-Barriuso
Journal:  Int J Mol Sci       Date:  2019-11-15       Impact factor: 5.923

9.  Retinal Ganglion Cells: Global Number, Density and Vulnerability to Glaucomatous Injury in Common Laboratory Mice.

Authors:  Marie Claes; Lieve Moons
Journal:  Cells       Date:  2022-08-29       Impact factor: 7.666

10.  Using retinal function to define ischemic exclusion criteria for animal models of glaucoma.

Authors:  Bailey G Hannon; Andrew J Feola; Brandon G Gerberich; A Thomas Read; Mark R Prausnitz; C Ross Ethier; Machelle T Pardue
Journal:  Exp Eye Res       Date:  2020-11-07       Impact factor: 3.770

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.