Short-term Rho-associated kinase inhibitor treatment accelerates primary keratinocyte growth while preserving stem cell characteristics

Somatic stem cells can be cultured in-vitro and are attractive for cell and gene therapies, but their slow growth in in-vitro culture affects survival and stemness and hinders clinical applications. Rho-associated kinase inhibitor (ROCKi) has been used to overcome these obstacles. However, it risks changing the characteristics of stem cells. We found that primary keratinocyte stem cells (KSCs) cultured with the ROCKi Y-27632 for six days exhibited rapid proliferation while maintaining the ability to differentiate. Importantly, after discontinuation of ROCKi treatment, KSC numbers and characteristics were indistinguishable from those in non-treated cultures. We further confirmed that ROCKi treatment resulted in the activation of AKT and ERK pathways, which could support cell survival and proliferation in keratinocytes. We thus concluded that accelerating keratinocyte expansion with short-term ROCKi treatment does not exhaust KSCs’ self-renewal and differentiation capacities, presenting a safe avenue for clinical applications.

[1]  G. Marsboom,et al.  Mitophagy Mediates Metabolic Reprogramming of Induced Pluripotent Stem Cells Undergoing Endothelial Differentiation. , 2021, The Journal of biological chemistry.

[2]  C. Lindskog,et al.  A single–cell type transcriptomics map of human tissues , 2021, Science Advances.

[3]  Xiuyuan Cheng,et al.  Detection of differentially abundant cell subpopulations in scRNA-seq data , 2021, Proceedings of the National Academy of Sciences.

[4]  C. Peano,et al.  Single-keratinocyte transcriptomic analyses identify different clonal types and proliferative potential mediated by FOXM1 in human epidermal stem cells , 2021, Nature Communications.

[5]  Y. Miao,et al.  Establishment of an Efficient Primary Culture System for Human Hair Follicle Stem Cells Using the Rho-Associated Protein Kinase Inhibitor Y-27632 , 2021, Frontiers in Cell and Developmental Biology.

[6]  W. Qasim,et al.  Ex vivo gene modification therapy for genetic skin diseases—recent advances in gene modification technologies and delivery , 2021, Experimental dermatology.

[7]  Raphael Gottardo,et al.  Integrated analysis of multimodal single-cell data , 2020, Cell.

[8]  S. Bondanza,et al.  Toward Combined Cell and Gene Therapy for Genodermatoses. , 2020, Cold Spring Harbor perspectives in biology.

[9]  N. Salomonis,et al.  Asymmetrically Segregated Mitochondria Provide Cellular Memory of Hematopoietic Stem Cell Replicative History and Drive HSC Attrition. , 2020, Cell stem cell.

[10]  S. Wheatley,et al.  Mitochondrial survivin reduces oxidative phosphorylation in cancer cells by inhibiting mitophagy , 2020, bioRxiv.

[11]  H. Cleland,et al.  A systematic review: Current trends and take rates of cultured epithelial autografts in the treatment of patients with burn injuries , 2019, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[12]  M. Hafner,et al.  Keratin 19 regulates cell cycle pathway and sensitivity of breast cancer cells to CDK inhibitors , 2019, Scientific Reports.

[13]  N. Sebire,et al.  Generation and clinical application of gene modified autologous epidermal sheets in Netherton syndrome - lessons learned from a phase 1 trial. , 2019, Human Gene Therapy.

[14]  Amir Bahat,et al.  Mitochondrial plasticity in cell fate regulation , 2019, The Journal of Biological Chemistry.

[15]  Wei Guo,et al.  SCINA: A Semi-Supervised Subtyping Algorithm of Single Cells and Bulk Samples , 2019, Genes.

[16]  R. Satija,et al.  Normalization and variance stabilization of single-cell RNA-seq data using regularized negative binomial regression , 2019, Genome Biology.

[17]  Fan Zhang,et al.  Fast, sensitive, and accurate integration of single cell data with Harmony , 2018, bioRxiv.

[18]  H. Ahmadieh,et al.  Intravitreal injection of a Rho-kinase inhibitor (fasudil) combined with bevacizumab versus bevacizumab monotherapy for diabetic macular oedema: a pilot randomised clinical trial , 2018, British Journal of Ophthalmology.

[19]  D. Haensel,et al.  Epithelial‐to‐mesenchymal transition in cutaneous wound healing: Where we are and where we are heading , 2018, Developmental dynamics : an official publication of the American Association of Anatomists.

[20]  S. Bicciato,et al.  Regeneration of the entire human epidermis using transgenic stem cells , 2017, Nature.

[21]  Russell B. Fletcher,et al.  Slingshot: cell lineage and pseudotime inference for single-cell transcriptomics , 2018, BMC Genomics.

[22]  Nektarios Tavernarakis,et al.  Mitochondrial biogenesis and clearance: a balancing act , 2017, The FEBS journal.

[23]  K. Rieger,et al.  Safety and Wound Outcomes Following Genetically Corrected Autologous Epidermal Grafts in Patients With Recessive Dystrophic Epidermolysis Bullosa. , 2016, JAMA.

[24]  Grace X. Y. Zheng,et al.  Massively parallel digital transcriptional profiling of single cells , 2016, Nature Communications.

[25]  S. Abhishek,et al.  Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets , 2016, Cell journal.

[26]  W. Ou,et al.  ROCK inhibitor Y27632 promotes proliferation and diminishes apoptosis of marmoset induced pluripotent stem cells by suppressing expression and activity of caspase 3. , 2016, Theriogenology.

[27]  J. Abraham,et al.  Long non-coding antisense RNA KRT7-AS is activated in gastric cancers and supports cancer cell progression by increasing KRT7 expression , 2015, Oncogene.

[28]  J. Pang,et al.  Y-27632, a ROCK Inhibitor, Promoted Limbal Epithelial Cell Proliferation and Corneal Wound Healing , 2015, PloS one.

[29]  J. Bos,et al.  Rap1 Spatially Controls ArhGAP29 To Inhibit Rho Signaling during Endothelial Barrier Regulation , 2015, Molecular and Cellular Biology.

[30]  D. McDermott,et al.  The effect of Rho kinase inhibition on long-term keratinocyte proliferation is rapid and conditional , 2014, Stem Cell Research & Therapy.

[31]  D. Epstein,et al.  Effects of Y27632 on keratinocyte procurement and wound healing , 2013, Clinical and experimental dermatology.

[32]  P. Gain,et al.  ROCK Inhibitor Enhances Adhesion and Wound Healing of Human Corneal Endothelial Cells , 2013, PloS one.

[33]  Xiang Luo,et al.  ROCK inhibition with Y27632 promotes the proliferation and cell cycle progression of cultured astrocyte from spinal cord , 2012, Neurochemistry International.

[34]  D. Kalderon,et al.  Drosophila Follicle Stem Cells are regulated by proliferation and niche adhesion as well as mitochondria and ROS , 2012, Nature Communications.

[35]  J. Srivastava,et al.  Dynamic actin remodeling during epithelial–mesenchymal transition depends on increased moesin expression , 2011, Molecular biology of the cell.

[36]  J. Shin,et al.  The Rho kinase inhibitor fasudil augments the number of functional endothelial progenitor cells in ex vivo cultures. , 2011, International journal of molecular medicine.

[37]  A. Satelli,et al.  Vimentin in cancer and its potential as a molecular target for cancer therapy , 2011, Cellular and Molecular Life Sciences.

[38]  Li Zhang,et al.  ROCK Inhibitor Y-27632 Suppresses Dissociation-Induced Apoptosis of Murine Prostate Stem/Progenitor Cells and Increases Their Cloning Efficiency , 2011, PloS one.

[39]  S. Ikawa,et al.  Epidermal FABP (FABP5) regulates keratinocyte differentiation by 13(S)-HODE-mediated activation of the NF-κB signaling pathway. , 2011, The Journal of investigative dermatology.

[40]  Utpal Banerjee,et al.  Mitochondrial Function Controls Proliferation and Early Differentiation Potential of Embryonic Stem Cells , 2011, Stem cells.

[41]  H. Baharvand,et al.  Long-term self-renewable feeder-free human induced pluripotent stem cell-derived neural progenitors. , 2011, Stem cells and development.

[42]  M. del Río,et al.  Ex-vivo gene therapy restores LEKTI activity and corrects the architecture of Netherton syndrome-derived skin grafts. , 2011, Molecular therapy : the journal of the American Society of Gene Therapy.

[43]  K. Kaibuchi,et al.  Rho-Kinase/ROCK: A Key Regulator of the Cytoskeleton and Cell Polarity , 2010, Cytoskeleton.

[44]  Yoshiki Sasai,et al.  Molecular pathway and cell state responsible for dissociation-induced apoptosis in human pluripotent stem cells. , 2010, Cell stem cell.

[45]  Craig Meyers,et al.  Human keratinocytes are efficiently immortalized by a Rho kinase inhibitor. , 2010, The Journal of clinical investigation.

[46]  A. Terunuma,et al.  Efficient procurement of epithelial stem cells from human tissue specimens using a Rho-associated protein kinase inhibitor Y-27632. , 2010, Tissue engineering. Part A.

[47]  M. Olson Applications for ROCK kinase inhibition. , 2008, Current opinion in cell biology.

[48]  Shuh Narumiya,et al.  Inhibition of the Rho/ROCK pathway reduces apoptosis during transplantation of embryonic stem cell‐derived neural precursors , 2008, Journal of neuroscience research.

[49]  K. Takakura,et al.  A postmarketing surveillance study of fasudil treatment after aneurysmal subarachnoid hemorrhage. , 2007, Surgical neurology.

[50]  S. Nishikawa,et al.  A ROCK inhibitor permits survival of dissociated human embryonic stem cells , 2007, Nature Biotechnology.

[51]  A. Hopkins,et al.  Organized migration of epithelial cells requires control of adhesion and protrusion through Rho kinase effectors. , 2007, American journal of physiology. Gastrointestinal and liver physiology.

[52]  F. Watt Stem cell fate and patterning in mammalian epidermis. , 2001, Current opinion in genetics & development.

[53]  D. Ponzin,et al.  p63 identifies keratinocyte stem cells , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[54]  Fumio Matsumura,et al.  Distinct Roles of Rock (Rho-Kinase) and Mlck in Spatial Regulation of Mlc Phosphorylation for Assembly of Stress Fibers and Focal Adhesions in 3t3 Fibroblasts , 2000, The Journal of cell biology.

[55]  S. Narumiya,et al.  Rho-associated Kinase ROCK Activates LIM-kinase 1 by Phosphorylation at Threonine 508 within the Activation Loop* , 2000, The Journal of Biological Chemistry.

[56]  Amy Li,et al.  Identification and isolation of candidate human keratinocyte stem cells based on cell surface phenotype. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[57]  S. Frisch,et al.  Disruption of epithelial cell-matrix interactions induces apoptosis , 1994, The Journal of cell biology.

[58]  F. Shishido,et al.  Effects of Fasudil Hydrochloride on Cerebral Blood Flow in Patients with Chronic Cerebral Infarction , 1993, Clinical neuropharmacology.

[59]  Y. Barrandon,et al.  Three clonal types of keratinocyte with different capacities for multiplication. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[60]  J. Mulliken,et al.  GRAFTING OF BURNS WITH CULTURED EPITHELIUM PREPARED FROM AUTOLOGOUS EPIDERMAL CELLS , 1981, The Lancet.

[61]  J. McGrath,et al.  Phase I study protocol for ex-vivo lentiviral gene therapy for the inherited skin disease, Netherton Syndrome. , 2013, Human gene therapy. Clinical development.

[62]  Y. Tokura,et al.  Epithelial-mesenchymal transition in the skin. , 2011, Journal of dermatological science.

[63]  H Green,et al.  Serial cultivation of strains of human epidermal keratinocytes: the formation of keratinizing colonies from single cells. , 1975, Cell.