Literature DB >> 23975727

A forensic path to RGC-5 cell line identification: lessons learned.

Raghu R Krishnamoorthy1, Abbot F Clark, Donald Daudt, Jamboor K Vishwanatha, Thomas Yorio.   

Abstract

In 2001, a transformed cell line RGC-5 was developed from the rat retina that was thought to be of retinal ganglion cell origin. Since that time many investigators have used this line in a wide variety of studies to understand better retinal ganglion cell activity, cell signaling, and neuroprotection. Recently, a publication emerged that claimed that this RGC-5 cell line was derived from mouse and not rat, and other studies also indicated the expression of certain proteins that typically were not associated with retinal ganglion cells. This certainly came as a shock not only to the originators of this cell line, but also to others who have been using this as an in vitro model of rat retinal ganglion cells. As a result, we undertook experiments to determine if the RGC-5 cell line currently in use may have been mischaracterized. We, indeed, found that the RGC-5 cell line was of mouse and not rat origin, as was claimed originally in the original research report. We further determined whether these cells were of retinal ganglion origin. Our findings showed conclusively that RGC-5 cells were, indeed, of mouse origin and, using additional cytogenetic profile testing, karyotyping, and genetic and protein profiling, we concluded that these cells were not of retinal ganglion cell origin, but were the cell line 661W, a mouse SV-40 T antigen transformed photoreceptor cell line. The 661W cell line also was present in the laboratory of the originating laboratory and probably resulted in cross-contamination. The present study reviews some of the errors that were made in misidentifying the RGC-5 cell line and offers some insight as to how this may have happened, and ways one can avoid mischaracterization of a potentially important cell line.

Entities:  

Keywords:  661W; RGC-5; cell misidentification; tissue culture

Mesh:

Substances:

Year:  2013        PMID: 23975727     DOI: 10.1167/iovs.13-12085

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  60 in total

1.  RGC-5 cells.

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Journal:  Invest Ophthalmol Vis Sci       Date:  2013-12-03       Impact factor: 4.799

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4.  Inhibition of TLR4 alleviates the inflammation and apoptosis of retinal ganglion cells in high glucose.

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5.  Endoplasmic reticulum stress promotes amyloid-beta peptides production in RGC-5 cells.

Authors:  Bingqian Liu; Yingting Zhu; Jiayi Zhou; Yantao Wei; Chongde Long; Mengfei Chen; Yunlan Ling; Jian Ge; Yehong Zhuo
Journal:  Cell Stress Chaperones       Date:  2014-03-19       Impact factor: 3.667

Review 6.  Endoplasmic reticulum stress and the unfolded protein responses in retinal degeneration.

Authors:  Sarah X Zhang; Emily Sanders; Steven J Fliesler; Joshua J Wang
Journal:  Exp Eye Res       Date:  2014-05-02       Impact factor: 3.467

7.  Molecular characterization of the human lens epithelium-derived cell line SRA01/04.

Authors:  Bailey A T Weatherbee; Joshua R Barton; Archana D Siddam; Deepti Anand; Salil A Lachke
Journal:  Exp Eye Res       Date:  2019-08-31       Impact factor: 3.467

Review 8.  G protein-coupled receptor 91 signaling in diabetic retinopathy and hypoxic retinal diseases.

Authors:  Jianyan Hu; Tingting Li; Xinhua Du; Qiang Wu; Yun-Zheng Le
Journal:  Vision Res       Date:  2017-06-23       Impact factor: 1.886

Review 9.  Regulation of Cell Behavior by Hydrostatic Pressure.

Authors:  Shaobao Liu; Ru Tao; Ming Wang; Jin Tian; Guy M Genin; Tian Jian Lu; Feng Xu
Journal:  Appl Mech Rev       Date:  2019-07-23       Impact factor: 7.281

10.  Cell surface translocation of annexin A2 facilitates glutamate-induced extracellular proteolysis.

Authors:  Mallika Valapala; Sayantan Maji; Julian Borejdo; Jamboor K Vishwanatha
Journal:  J Biol Chem       Date:  2014-04-17       Impact factor: 5.157

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