Interleukin-13 increases the stemness of limbal epithelial stem cells cultures.

This study aimed to determine the effect of interleukin-13 (IL13) on the stemness, differentiation, proliferation, clonogenicity, and morphology of cultured limbal epithelial cells (LECs). Human limbal explants were used to culture LECs up to the second passage (P0-P2) with or without IL13 (IL13+ an...

Full description

Bibliographic Details
Main Authors: Peter Trosan, Joao Victor Cabral, Ingrida Smeringaiova, Pavel Studeny, Katerina Jirsova
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2022-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0272081
_version_ 1811188962931245056
author Peter Trosan
Joao Victor Cabral
Ingrida Smeringaiova
Pavel Studeny
Katerina Jirsova
author_facet Peter Trosan
Joao Victor Cabral
Ingrida Smeringaiova
Pavel Studeny
Katerina Jirsova
author_sort Peter Trosan
collection DOAJ
description This study aimed to determine the effect of interleukin-13 (IL13) on the stemness, differentiation, proliferation, clonogenicity, and morphology of cultured limbal epithelial cells (LECs). Human limbal explants were used to culture LECs up to the second passage (P0-P2) with or without IL13 (IL13+ and IL13-, respectively). Cells were analyzed by qPCR (for the expression of ΔNp63α, BMI-1, keratin (K) 3, K7, K12, K14, K17, mucin 4, and MKI67) and immunofluorescence staining for p63α. The clonogenic ability was determined by colony-forming assay (CFA), and their metabolic activity was measured by WST-1 assay. The results of the CFA showed a significantly increased clonogenic ability in P1 and P2 cultures when LECs were cultured with IL13. In addition, the expression of putative stem cell markers (ΔNp63α, K14, and K17) was significantly higher in all IL13+ cultures compared to IL13-. Similarly, immunofluorescence analysis showed a significantly higher percentage of p63α positive cells in P2 cultures with IL13 than without it. LECs cultures without IL13 lost their cuboidal morphology with a high nucleocytoplasmic ratio after P1. The use of IL13 also led to significantly higher proliferation in P2, which can be reflected by a higher ability to reach confluence in P2 cultures. On the other hand, IL13 had no effect on corneal epithelial cell differentiation (K3 and K12 expression), and the expression of the conjunctival marker K7 significantly increased in all IL13+ cultures compared to the respective cell culture without IL13. This study showed that IL13 enhanced the stemness of LECs by increasing the clonogenicity and the expression of putative stem cell markers of LECs while maintaining their stem cell morphology. We established IL13 as a culture supplement for LESCs, which increases their stemness potential in culture, even after the second passage, and may lead to the greater success of LESCs transplantation in patients with LSCD.
first_indexed 2024-04-11T14:26:46Z
format Article
id doaj.art-b3697db87da64a3ea71c3ccc472d5531
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-04-11T14:26:46Z
publishDate 2022-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-b3697db87da64a3ea71c3ccc472d55312022-12-22T04:18:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032022-01-01178e027208110.1371/journal.pone.0272081Interleukin-13 increases the stemness of limbal epithelial stem cells cultures.Peter TrosanJoao Victor CabralIngrida SmeringaiovaPavel StudenyKaterina JirsovaThis study aimed to determine the effect of interleukin-13 (IL13) on the stemness, differentiation, proliferation, clonogenicity, and morphology of cultured limbal epithelial cells (LECs). Human limbal explants were used to culture LECs up to the second passage (P0-P2) with or without IL13 (IL13+ and IL13-, respectively). Cells were analyzed by qPCR (for the expression of ΔNp63α, BMI-1, keratin (K) 3, K7, K12, K14, K17, mucin 4, and MKI67) and immunofluorescence staining for p63α. The clonogenic ability was determined by colony-forming assay (CFA), and their metabolic activity was measured by WST-1 assay. The results of the CFA showed a significantly increased clonogenic ability in P1 and P2 cultures when LECs were cultured with IL13. In addition, the expression of putative stem cell markers (ΔNp63α, K14, and K17) was significantly higher in all IL13+ cultures compared to IL13-. Similarly, immunofluorescence analysis showed a significantly higher percentage of p63α positive cells in P2 cultures with IL13 than without it. LECs cultures without IL13 lost their cuboidal morphology with a high nucleocytoplasmic ratio after P1. The use of IL13 also led to significantly higher proliferation in P2, which can be reflected by a higher ability to reach confluence in P2 cultures. On the other hand, IL13 had no effect on corneal epithelial cell differentiation (K3 and K12 expression), and the expression of the conjunctival marker K7 significantly increased in all IL13+ cultures compared to the respective cell culture without IL13. This study showed that IL13 enhanced the stemness of LECs by increasing the clonogenicity and the expression of putative stem cell markers of LECs while maintaining their stem cell morphology. We established IL13 as a culture supplement for LESCs, which increases their stemness potential in culture, even after the second passage, and may lead to the greater success of LESCs transplantation in patients with LSCD.https://doi.org/10.1371/journal.pone.0272081
spellingShingle Peter Trosan
Joao Victor Cabral
Ingrida Smeringaiova
Pavel Studeny
Katerina Jirsova
Interleukin-13 increases the stemness of limbal epithelial stem cells cultures.
PLoS ONE
title Interleukin-13 increases the stemness of limbal epithelial stem cells cultures.
title_full Interleukin-13 increases the stemness of limbal epithelial stem cells cultures.
title_fullStr Interleukin-13 increases the stemness of limbal epithelial stem cells cultures.
title_full_unstemmed Interleukin-13 increases the stemness of limbal epithelial stem cells cultures.
title_short Interleukin-13 increases the stemness of limbal epithelial stem cells cultures.
title_sort interleukin 13 increases the stemness of limbal epithelial stem cells cultures
url https://doi.org/10.1371/journal.pone.0272081
work_keys_str_mv AT petertrosan interleukin13increasesthestemnessoflimbalepithelialstemcellscultures
AT joaovictorcabral interleukin13increasesthestemnessoflimbalepithelialstemcellscultures
AT ingridasmeringaiova interleukin13increasesthestemnessoflimbalepithelialstemcellscultures
AT pavelstudeny interleukin13increasesthestemnessoflimbalepithelialstemcellscultures
AT katerinajirsova interleukin13increasesthestemnessoflimbalepithelialstemcellscultures