TY - JOUR
T1 - Characterization of rabbit limbal epithelial side population cells using RNA sequencing and single-cell qRT-PCR
AU - Kameishi, Sumako
AU - Umemoto, Terumasa
AU - Matsuzaki, Yu
AU - Fujita, Masako
AU - Okano, Teruo
AU - Kato, Takashi
AU - Yamato, Masayuki
N1 - Funding Information:
We thank Dr. Hiroaki Sugiyama, Dr. Ryo Takagi, and Dr. Makoto Kondo (Tokyo Women's Medical University) for their useful comments and technical criticism. This study was partially supported by a Grant-in-Aid for Japan Society for the Promotion of Science (JSPS) Fellows (Grant number: 7346 ), Creation of innovation centers for advanced interdisciplinary research areas Program in the Project for Developing Innovation Systems ‘ Cell Sheet Tissue Engineering Center (CSTEC), Japan.
PY - 2016/5/6
Y1 - 2016/5/6
N2 - Corneal epithelial stem cells reside in the limbus, a transitional zone between the cornea and conjunctiva, and are essential for maintaining homeostasis in the corneal epithelium. Although our previous studies demonstrated that rabbit limbal epithelial side population (SP) cells exhibit stem cell-like phenotypes with Hoechst 33342 staining, the different characteristics and/or populations of these cells remain unclear. Therefore, in this study, we determined the gene expression profiles of limbal epithelial SP cells by RNA sequencing using not only present public databases but also contigs that were created by de novo transcriptome assembly as references for mapping. Our transcriptome data indicated that limbal epithelial SP cells exhibited a stem cell-like phenotype compared with non-SP cells. Importantly, gene ontology analysis following RNA sequencing demonstrated that limbal epithelial SP cells exhibited significantly enhanced expression of mesenchymal/endothelial cell markers rather than epithelial cell markers. Furthermore, single-cell quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) demonstrated that the limbal epithelial SP population consisted of at least two immature cell populations with endothelial- or mesenchymal-like phenotypes. Therefore, our present results may propose the presence of a novel population of corneal epithelial stem cells distinct from conventional epithelial stem cells.
AB - Corneal epithelial stem cells reside in the limbus, a transitional zone between the cornea and conjunctiva, and are essential for maintaining homeostasis in the corneal epithelium. Although our previous studies demonstrated that rabbit limbal epithelial side population (SP) cells exhibit stem cell-like phenotypes with Hoechst 33342 staining, the different characteristics and/or populations of these cells remain unclear. Therefore, in this study, we determined the gene expression profiles of limbal epithelial SP cells by RNA sequencing using not only present public databases but also contigs that were created by de novo transcriptome assembly as references for mapping. Our transcriptome data indicated that limbal epithelial SP cells exhibited a stem cell-like phenotype compared with non-SP cells. Importantly, gene ontology analysis following RNA sequencing demonstrated that limbal epithelial SP cells exhibited significantly enhanced expression of mesenchymal/endothelial cell markers rather than epithelial cell markers. Furthermore, single-cell quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) demonstrated that the limbal epithelial SP population consisted of at least two immature cell populations with endothelial- or mesenchymal-like phenotypes. Therefore, our present results may propose the presence of a novel population of corneal epithelial stem cells distinct from conventional epithelial stem cells.
KW - Corneal epithelial stem cells
KW - Gene expression profile
KW - Limbal epithelial side population
KW - RNA sequencing
KW - Single-cell qRT-PCR
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U2 - 10.1016/j.bbrc.2015.10.155
DO - 10.1016/j.bbrc.2015.10.155
M3 - Article
C2 - 26546824
AN - SCOPUS:84964683575
SN - 0006-291X
VL - 473
SP - 704
EP - 709
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -