Effects of flow-induced shear stress on limbal epithelial stem cell growth and enrichment

• Published in: PloS one 2014-03, Vol.9 (3), p.e93023-e93023
• Main Authors: Kang, Yun Gyeong, Shin, Ji Won, Park, So Hee, Oh, Min-Jae, Park, Hyo Soon, Shin, Jung-Woog, Kim, Su-Hyang
• Format: Article
• Language: English
• Subjects: Analysis; Animals; Biology and Life Sciences; Biomarkers; Biomedical engineering; Biomimetics; Bioreactors; Bmi protein; Cell culture; Cell Proliferation; Cornea; Culture techniques; Differentiation; Engineering; Engineering and Technology; Epithelial cells; Epithelial Cells - cytology; Epithelial Cells - metabolism; Experimental methods; Flow; Gene Expression; Limbus Corneae - cytology; Mechanical stimuli; Medicine and Health Sciences; Metabolic disorders; Notch1 protein; Rabbits; Rodents; Shear flow; Shear Strength; Shear stress; Shear stresses; Steady flow; Stem cell research; Stem cells; Stem Cells - cytology; Stem Cells - metabolism; Stress, Mechanical; Studies; Therapeutic applications; Tissues
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0093023

The roles of limbal epithelial stem cells (LESCs) are widely recognized, but for these cells to be utilized in basic research and potential clinical applications, researchers must be able to efficiently isolate them and subsequently maintain their stemness in vitro. We aimed to develop a biomimetic environment for LESCs involving cells from their in vivo niche and the principle of flow-induced shear stress, and to subsequently demonstrate the potential of this novel paradigm. LESCs, together with neighboring cells, were isolated from the minced limbal tissues of rabbits. At days 8 and 9 of culture, the cells were exposed to a steady flow or intermittent flow for 2 h per day in a custom-designed bioreactor. The responses of LESCs and epithelial cells were assessed at days 12 and 14. LESCs and epithelial cells responded to both types of flow. Proliferation of LESCs, as assessed using a BrdU assay, was increased to a greater extent under steady flow conditions. Holoclones were found under intermittent flow, indicating that differentiation into transient amplifying cells had occurred. Immunofluorescent staining of Bmi-1 suggested that steady flow has a positive effect on the maintenance of stemness. This finding was confirmed by real-time PCR. Notch-1 and p63 were more sensitive to intermittent flow, but this effect was transient. K3 and K12 expression, indicative of differentiation of LESCs into epithelial cells, was induced by flow and lasted longer under intermittent flow conditions. In summary, culture of LESCs in a bioreactor under a steady flow paradigm, rather than one of intermittent flow, is beneficial for both increasing proliferation and maintaining stemness. Conversely, intermittent flow appears to induce differentiation of LESCs. This novel experimental method introduces micro-mechanical stimuli to traditional culture techniques, and has potential for regulating the proliferation and differentiation of LESCs in vitro, thereby facilitating research in this field.