A rapid separation of two distinct populations of mouse corneal epithelial cells with limbal stem cell characteristics by centrifugation on Percoll gradient

Magdalena Krulova, Katerina Pokorna, Anna Lencova, Jan Fric, Alena Zajicova, Martin Filipec, John V. Forrester, Vladimir Holan

Research output: Contribution to journalArticle

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Abstract

PURPOSE. To detect and isolate cells with stem cell (SC) characteristics in the limbus of the mouse.

METHODS. Limbal tissues from BALB/c mice were trypsin-dissociated and separated on the gradient Percoll (Fluka, Buchs, Switzerland). Several fractions were isolated and characterized by real-time PCR for the presence of limbal SC markers and differentiation markers of corneal epithelial cells by flow cytometry for the determination of the side-population (SP) phenotype and growth properties in vitro.

RESULTS. Cells retained in the lightest fraction (40% Percoll) and in the densest fraction (80% Percoll) of the gradient were both enriched for populations with a high expression of the SC markers ABCG2 and Lgr5 and also expressing the SP phenotype. However, the lightest fraction (representing approximately 12% of total limbal cells) contained cells with the strongest spontaneous proliferative capacity and expressed the corneal epithelial differentiation marker K12. In contrast the densest fraction (< 7% of original cells) was K12 negative and contained small nonspontaneously proliferating cells, which instead were positive for p63. Unexpectedly, cells from this fraction had the highest proliferative activity when cultured on a 3T3 feeder cell monolayer.

CONCLUSIONS. These findings demonstrate the presence of two distinct populations of corneal epithelial cells with limbal SC characteristics, based on differential expression of the keratin-specific marker K12 and transcription factor p63, and suggest a difference in developmental stage of the two populations, with the K12(-)p63(+) population being closer to the primitive limbal SC.

Original languageEnglish
Pages (from-to)3903-3908
Number of pages6
JournalInvestigative Ophthalmology & Visual Science
Volume49
Issue number9
Early online date9 May 2008
DOIs
Publication statusPublished - Sep 2008

Keywords

  • amniotic membrane
  • transporter ABCG2
  • expression
  • phenotype
  • keratin
  • transplantation
  • identification
  • migration
  • capacity

Cite this

A rapid separation of two distinct populations of mouse corneal epithelial cells with limbal stem cell characteristics by centrifugation on Percoll gradient. / Krulova, Magdalena; Pokorna, Katerina; Lencova, Anna; Fric, Jan; Zajicova, Alena; Filipec, Martin; Forrester, John V.; Holan, Vladimir.

In: Investigative Ophthalmology & Visual Science, Vol. 49, No. 9, 09.2008, p. 3903-3908.

Research output: Contribution to journalArticle

Krulova, Magdalena ; Pokorna, Katerina ; Lencova, Anna ; Fric, Jan ; Zajicova, Alena ; Filipec, Martin ; Forrester, John V. ; Holan, Vladimir. / A rapid separation of two distinct populations of mouse corneal epithelial cells with limbal stem cell characteristics by centrifugation on Percoll gradient. In: Investigative Ophthalmology & Visual Science. 2008 ; Vol. 49, No. 9. pp. 3903-3908.
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title = "A rapid separation of two distinct populations of mouse corneal epithelial cells with limbal stem cell characteristics by centrifugation on Percoll gradient",
abstract = "PURPOSE. To detect and isolate cells with stem cell (SC) characteristics in the limbus of the mouse.METHODS. Limbal tissues from BALB/c mice were trypsin-dissociated and separated on the gradient Percoll (Fluka, Buchs, Switzerland). Several fractions were isolated and characterized by real-time PCR for the presence of limbal SC markers and differentiation markers of corneal epithelial cells by flow cytometry for the determination of the side-population (SP) phenotype and growth properties in vitro.RESULTS. Cells retained in the lightest fraction (40{\%} Percoll) and in the densest fraction (80{\%} Percoll) of the gradient were both enriched for populations with a high expression of the SC markers ABCG2 and Lgr5 and also expressing the SP phenotype. However, the lightest fraction (representing approximately 12{\%} of total limbal cells) contained cells with the strongest spontaneous proliferative capacity and expressed the corneal epithelial differentiation marker K12. In contrast the densest fraction (< 7{\%} of original cells) was K12 negative and contained small nonspontaneously proliferating cells, which instead were positive for p63. Unexpectedly, cells from this fraction had the highest proliferative activity when cultured on a 3T3 feeder cell monolayer.CONCLUSIONS. These findings demonstrate the presence of two distinct populations of corneal epithelial cells with limbal SC characteristics, based on differential expression of the keratin-specific marker K12 and transcription factor p63, and suggest a difference in developmental stage of the two populations, with the K12(-)p63(+) population being closer to the primitive limbal SC.",
keywords = "amniotic membrane, transporter ABCG2, expression, phenotype, keratin, transplantation, identification, migration, capacity",
author = "Magdalena Krulova and Katerina Pokorna and Anna Lencova and Jan Fric and Alena Zajicova and Martin Filipec and Forrester, {John V.} and Vladimir Holan",
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T1 - A rapid separation of two distinct populations of mouse corneal epithelial cells with limbal stem cell characteristics by centrifugation on Percoll gradient

AU - Krulova, Magdalena

AU - Pokorna, Katerina

AU - Lencova, Anna

AU - Fric, Jan

AU - Zajicova, Alena

AU - Filipec, Martin

AU - Forrester, John V.

AU - Holan, Vladimir

PY - 2008/9

Y1 - 2008/9

N2 - PURPOSE. To detect and isolate cells with stem cell (SC) characteristics in the limbus of the mouse.METHODS. Limbal tissues from BALB/c mice were trypsin-dissociated and separated on the gradient Percoll (Fluka, Buchs, Switzerland). Several fractions were isolated and characterized by real-time PCR for the presence of limbal SC markers and differentiation markers of corneal epithelial cells by flow cytometry for the determination of the side-population (SP) phenotype and growth properties in vitro.RESULTS. Cells retained in the lightest fraction (40% Percoll) and in the densest fraction (80% Percoll) of the gradient were both enriched for populations with a high expression of the SC markers ABCG2 and Lgr5 and also expressing the SP phenotype. However, the lightest fraction (representing approximately 12% of total limbal cells) contained cells with the strongest spontaneous proliferative capacity and expressed the corneal epithelial differentiation marker K12. In contrast the densest fraction (< 7% of original cells) was K12 negative and contained small nonspontaneously proliferating cells, which instead were positive for p63. Unexpectedly, cells from this fraction had the highest proliferative activity when cultured on a 3T3 feeder cell monolayer.CONCLUSIONS. These findings demonstrate the presence of two distinct populations of corneal epithelial cells with limbal SC characteristics, based on differential expression of the keratin-specific marker K12 and transcription factor p63, and suggest a difference in developmental stage of the two populations, with the K12(-)p63(+) population being closer to the primitive limbal SC.

AB - PURPOSE. To detect and isolate cells with stem cell (SC) characteristics in the limbus of the mouse.METHODS. Limbal tissues from BALB/c mice were trypsin-dissociated and separated on the gradient Percoll (Fluka, Buchs, Switzerland). Several fractions were isolated and characterized by real-time PCR for the presence of limbal SC markers and differentiation markers of corneal epithelial cells by flow cytometry for the determination of the side-population (SP) phenotype and growth properties in vitro.RESULTS. Cells retained in the lightest fraction (40% Percoll) and in the densest fraction (80% Percoll) of the gradient were both enriched for populations with a high expression of the SC markers ABCG2 and Lgr5 and also expressing the SP phenotype. However, the lightest fraction (representing approximately 12% of total limbal cells) contained cells with the strongest spontaneous proliferative capacity and expressed the corneal epithelial differentiation marker K12. In contrast the densest fraction (< 7% of original cells) was K12 negative and contained small nonspontaneously proliferating cells, which instead were positive for p63. Unexpectedly, cells from this fraction had the highest proliferative activity when cultured on a 3T3 feeder cell monolayer.CONCLUSIONS. These findings demonstrate the presence of two distinct populations of corneal epithelial cells with limbal SC characteristics, based on differential expression of the keratin-specific marker K12 and transcription factor p63, and suggest a difference in developmental stage of the two populations, with the K12(-)p63(+) population being closer to the primitive limbal SC.

KW - amniotic membrane

KW - transporter ABCG2

KW - expression

KW - phenotype

KW - keratin

KW - transplantation

KW - identification

KW - migration

KW - capacity

U2 - 10.1167/iovs.08-1987

DO - 10.1167/iovs.08-1987

M3 - Article

VL - 49

SP - 3903

EP - 3908

JO - Investigative Ophthalmology & Visual Science

JF - Investigative Ophthalmology & Visual Science

SN - 0146-0404

IS - 9

ER -