» Articles » PMID: 32396634

KLF4 Coordinates Corneal Epithelial Apical-Basal Polarity and Plane of Cell Division and Is Downregulated in Ocular Surface Squamous Neoplasia

Overview
Specialty Ophthalmology
Date 2020 May 13
PMID 32396634
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: Previously, we demonstrated that Krüppel-like factor 4 (KLF4) promotes corneal epithelial (CE) homeostasis by suppressing epithelial-mesenchymal transition (EMT) and TGF-β signaling. As TGF-β affects epithelial apicobasal polarity (ABP) and plane of division, we investigated the role of KLF4 in these processes.

Methods: Klf4 was ablated in adult ternary transgenic Klf4Δ/ΔCE (Klf4LoxP/LoxP/Krt12rtTA/rtTA/Tet-O-Cre) mouse CE using doxycycline chow. ABP and plane of division markers' expression in Klf4Δ/ΔCE and human ocular surface squamous neoplasia (OSSN) tissues relative to controls was evaluated by quantitative PCR, immunoblots, and/or immunofluorescent staining.

Results: Klf4Δ/ΔCE CE cells displayed downregulation of apical Pals1 and Crumbs1, apicolateral Par3, and basolateral Scribble, as well as upregulation of Rho family GTPase Cdc42, suggesting disruption of ABP. Phalloidin staining revealed that the Klf4Δ/ΔCE CE actin cytoskeleton is disrupted. Klf4Δ/ΔCE cells favored vertical plane of division within 67.5° to 90° of the CE basement membrane (39% and 47% of the dividing cells relative to 23% and 26% in the control based on phospho-histone-H3 and survivin, respectively), resulting in more dividing cells within the Klf4Δ/ΔCE CE as reported previously. KLF4 was downregulated in human OSSN tissues that displayed EMT and downregulation of PAR3, PALS1, and SCRIB, consistent with a protective role for KLF4.

Conclusions: By demonstrating that Klf4 ablation affects CE expression of ABP markers and Cdc42, cytoskeletal actin organization, and the plane of cell division and that KLF4 is downregulated in OSSN tissues that display EMT and lack ABP, these results elucidate the key integrative role of KLF4 in coordinating CE cell polarity and plane of division, loss of which results in OSSN.

Citing Articles

A dynamic co-expression approach reveals Gins2 as a potential upstream modulator of HNSCC metastasis.

Khayer N, Shabani S, Jalessi M, Joghataei M, Mahjoubi F Sci Rep. 2025; 15(1):3322.

PMID: 39865116 PMC: 11770085. DOI: 10.1038/s41598-024-82668-1.


Clinically correlated dose of the amniotic membrane extract is superior to its transplantation in corneal wound healing.

Korkmaz I, Kocamanoglu M, Gurdal M, Arici M, Yaman B, Palamar M Mol Vis. 2024; 30:188-199.

PMID: 39563677 PMC: 11575842.


The Upregulation of Leucine-Rich Repeat Containing 1 Expression Activates Hepatic Stellate Cells and Promotes Liver Fibrosis by Stabilizing Phosphorylated Smad2/3.

Wang Y, Li X, Guan X, Song Z, Liu H, Guan Z Int J Mol Sci. 2024; 25(5).

PMID: 38473980 PMC: 10932271. DOI: 10.3390/ijms25052735.


Intercellular Communication in Airway Epithelial Cell Regeneration: Potential Roles of Connexins and Pannexins.

Badaoui M, Chanson M Int J Mol Sci. 2023; 24(22).

PMID: 38003349 PMC: 10671439. DOI: 10.3390/ijms242216160.


Molecular nature of ocular surface barrier function, diseases that affect it, and its relevance for ocular drug delivery.

Kaur S, Sohnen P, Swamynathan S, Du Y, Espana E, Swamynathan S Ocul Surf. 2023; 30:3-13.

PMID: 37543173 PMC: 10837323. DOI: 10.1016/j.jtos.2023.08.001.


References
1.
Yu T, Chen X, Zhang W, Li J, Xu R, Wang T . Krüppel-like factor 4 regulates intestinal epithelial cell morphology and polarity. PLoS One. 2012; 7(2):e32492. PMC: 3286469. DOI: 10.1371/journal.pone.0032492. View

2.
Yori J, Johnson E, Zhou G, Jain M, Keri R . Kruppel-like factor 4 inhibits epithelial-to-mesenchymal transition through regulation of E-cadherin gene expression. J Biol Chem. 2010; 285(22):16854-63. PMC: 2878056. DOI: 10.1074/jbc.M110.114546. View

3.
Yu M, Hao B, Zhan Y, Luo G . Krüppel-like factor 4 expression in solid tumor prognosis: A meta-analysis. Clin Chim Acta. 2018; 485:50-59. DOI: 10.1016/j.cca.2018.06.030. View

4.
Rowland B, Peeper D . KLF4, p21 and context-dependent opposing forces in cancer. Nat Rev Cancer. 2005; 6(1):11-23. DOI: 10.1038/nrc1780. View

5.
Tiwari A, Swamynathan S, Alexander N, Gnalian J, Tian S, Kinchington P . KLF4 Regulates Corneal Epithelial Cell Cycle Progression by Suppressing Canonical TGF-β Signaling and Upregulating CDK Inhibitors P16 and P27. Invest Ophthalmol Vis Sci. 2019; 60(2):731-740. PMC: 6383833. DOI: 10.1167/iovs.18-26423. View