1School of Biomedical Sciences, Faculty of Health and Institute of Health & Biomedical Innovation,

Queensland University of Technology, 2 George Street, Brisbane, QLD 4001, Australia 2Queensland Eye Institute, 140 Melbourne Street, South Brisbane, QLD 4101, Australia Correspondence should be addressed to Neil A. Richardson; [email protected] Received 29 February 2016; Accepted 13 June 2016 Academic Editor: Silvia Brunelli

Copyright © 2016 Thomas A. Hogerheyde et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Scaffolds prepared from silk fibroin derived from cocoons of the domesticated silkworm moth Bombyx mori have demonstrated potential to support the attachment and growth of human limbal epithelial (HLE) cells in vitro. In this study, we attempted to further optimize protocols to promote the expansion of HLE cells on B. mori silk fibroin- (BMSF-) based scaffolds. BMSF films were initially coated with different extracellular matrix proteins and then analysed for their impact on corneal epithelial cell adhesion, cell morphology, and culture confluency. Results showed that collagen I, collagen III, and collagen IV consistently improved HCET cell adherence, promoted an elongated cell morphology, and increased culture confluency. By contrast, ECM coating had no significant effect on the performance of primary HLE cells cultured on BMSF films. In the second part of this study, primary HLE cells were grown on BMSF films in the presence of medium (SHEM) supplemented with keratinocyte growth factor (KGF) and the Rho kinase inhibitor, Y-27632. The results demonstrated that SHEM medium supplemented with KGF and Y-27632 dramatically increased expression of corneal differentiation markers, keratin 3 and keratin 12, whereas expression of the progenitor marker, p63, did not appear to be significantly influenced by the choice of culture medium.

Corneal epithelial progenitor cells are essential for maintenance of a smooth and transparent ocular surface. These so-called “corneal stem cells” are concentrated within the peripheral or limbal margin of the cornea [1] and express molecular markers typical of epithelial progenitor cells including the transcription factor p63 [2–4]. In contrast, mature corneal epithelial cells that cover the central cornea and suprabasal layers of the limbal epithelium are defined by coexpression of keratins 3 and 12 [1, 5–7].

Loss of corneal epithelial progenitor cells through disease or injury leads to a painful and blinding condition known

1. as limbal stem cell deficiency (LSCD) [8–10]. Classic symptoms of LSCD include coverage of the corneal surface with

conjunctivalepithelial cells and vascularizationof the corneal stroma. Strategies available for treating LSCD are based upon implantation of corneal epithelial progenitor cells derived from either an autologous or donor tissue source [11, 12]. Commonly, the epithelial progenitor cells are cultivated and implanted while attached to some form of scaffold. The most popular choice of scaffold for cultivated corneal epithelial implants is denuded amniotic membrane (AM). Limitations associatedwiththeuseofAM,however,includingpoortransparency and risk of disease transmission [13], have encouraged the development of alternative scaffolds such as membranes derived from the silk structural protein, fibroin [14].

In recent years, scaffolds fabricated from silk fibroin produced by the domesticated silkworm moth Bombyx mori (BMSF) have demonstrated potential for ophthalmic use

due to their unique combination of tensile strength, controlledbiodegradability,transparency,andcompatibilitywith a range of ocular cell types [14–19]. For example, BMSFcoated surfaces and freestanding membranes support the attachment, growth, and differentiation of human corneal epithelial progenitor cells [14, 15, 20]. In these prior studies, epithelial cell attachment to BMSF has been facilitated through the use of serum-supplemented culture medium. Further improvements in corneal epithelial cell attachment and growth, however, may yet be achieved by coating the BMSF with purified extracellular matrix (ECM) proteins. Moreover, comparative studies of culture media for corneal epithelial progenitor cell growth on BMSF are lacking. In particular, there is mounting evidence that increased selfrenewal and differentiation of cultured stem cells from ocular tissues can be achieved through the addition of the Rho kinase inhibitor, Y-27632, and keratinocyte growth factor (KGF) to culture medium [21–23]. The purpose of the present study was therefore to determine whether current protocols for the ex vivo expansion of human limbal epithelial (HLE) cell cultures on BMSF films could be improved by either (1) coating fibroin with specific ECM proteins or (2) utilising medium supplemented with Y-27632 and KGF. Previous investigations conducted on the use of BMSF-based scaffolds to support corneal epithelial cultures have used both immortalised and primary corneal epithelial cells [14, 15, 17, 24– 26]. For comparative purposes, in the first part of this study, the effect of coating BMSF with ECM was therefore assessed using both an immortalised corneal epithelial cell line (HCET) and primary HLE cells. Cultures were assessed for cell adhesion, cell morphology, and culture confluence. In the second part of this study, the effect of different culture media on the expression of markers associated with progenitor or differentiated phenotypes was assessed in primary HLE cell cultures established on fibroin films.

1. 2.1. Preparation of BMSF Films. B. mori cocoons with the pupa removed were supplied by Tajima Shoji Co. Ltd. (Yokohama, Japan). Aqueous solutions of silk fibroin (4% w/v) prepared from B. mori cocoons were processed using materials and techniques described previously and used within 1 month [14, 15]. Fibroin solution was poured into 24- or 96-well or T25 flasks to cast fibroin coatings. To assist drying, fibroin coatings were placed at room temperature (RT) in a fan-driven oven for 12h and then water annealed (with a beaker of water) at 80kPa in a vacuum chamber for 6h at RT. Fibroin surfaces were sterilised in 70% ethanol for 30min and then washed three times in PBS.
2. 2.2. Coating of BMSF with ECM. BMSF-coated 24- and 96well tissue culture plates were coated with ECM proteins

1. at 5 g/mL to promote corneal reepithelialisation. Collagen I (Cell Matrix), collagen III (Millipore), collagen IV (Sigma-Aldrich), fibronectin and laminin (both from SigmaAldrich), and vitronectin (Promega) were diluted to 5 g/mL in PBS, applied to fibroin surfaces, and then dried at RT in a fan-driven oven for 12h.

1. 2.3. Establishment of HCE-T and Primary HLE Cells
2. 2.4. Cell Attachment Assay. HCE-T or HLE cells were seeded intofibroin-coatedwellsatadensityof105 cells/cm2.Toavoid the unintended inclusion of cell attachment factors from serum-supplemented media, HCE-T cells were suspended

Table 1: Oligonucleotide primers used for qPCR analysis. Target Sequence 󸀠 󸀠 Keratin 3

Forward primer CCTCTACGACGCTGAGCTATC Reverse primer CCAGGGAGCGATTATTGTCCAT

Forward primer CTCTCCTCGCAGAGTGTGATA Reverse primer AACTAGAACCAAACATGGAAGC

Keratin 12

Forward primer GTCATTTGATTCGAGTAGAGGGG Reverse primer CTGGGGTGGCTCATAAGGT

p63

Forward primer CATGTACGTTGCTATCCAGGC Reverse primer CTCCTTAATGTCACGCACGAT

Beta-actin

in keratinocyte serum-free medium (KSFM; Thermo Fisher Scientific) containing 0.09mM calcium supplemented with 30mg/mL bovine pituitary extract, 0.2ng/mL EGF, and ampicillin/streptomycin. Plates were incubated at 37∘C in 5% CO2 for 90min, washed once in PBS, and then fixed using 4% formaldehyde.Numbersofadherentcellsweredeterminedby staining cultures with Hoechst dye (Invitrogen) in 100mM HEPES buffer for 1h at RT to visualise cell nuclei. Cells were then washed 3 times in distilled water, visualised via fluorescent microscopy, and photographed using a standardised matrix of five (10x) fields of view. Cell numbers were determined manually using ImageJ software. This process was repeated using primary HLE cells.

1. 2.5. Cellular Eccentricity and Confluency. To examine changes in cellular eccentricity and confluency, 3 104 HCE-T cells/cm2 were seeded into 96-well ECM-coated fibroin plates in DKSFM. Plates were incubated inside the IncuCyte ZOOM live cell analysis system (Essen Bioscience) for 72 hours with photographs captured at hourly intervals. Subsequently after creating a processing definition, a set of basic metrics were analysed using phase object analysis to determine changes in cellular eccentricity (ranges from 0 to 1 with a perfect circle having a value of 0) and confluency (the percentage of the image area that is occupied by cells).
2. 2.6. Phenotypic Analysis of HLE Cultures Grown in BMSFCoated Wells. To assess potential differences in the phenotype of cells cultured in two different media on BMSF-coated surfaces, two markers of corneal epithelial cell phenotype, p63 (progenitor marker) and keratin pair 3/12 (stratifying, differentiated cells), were examined. A polyclonal rabbit antibody to p63 (1:100 dilution, BioLegend) and a mouse monoclonalantibodytocytokeratinpair3/12(1:700dilution, Millipore) were used to perform immunocytochemistry. Initially, HCE cells on BMSF-coated wells were blocked in 5% normal goat serum (NGS) in PBS containing 0.5% Triton X-100 for 30min. Primary antibodies diluted in 1% NGS were subsequently applied at RT for 1h. Wells were washed

1. 3 times in PBS to remove unbound primary antibody before thesecondaryantibody(1:200dilution,AlexaFluor488antimouseorAlexaFluor594anti-rabbit;Invitrogen)wasapplied at RT for 20min.

1. 2.7. RNA Isolation. HLE cells cultured on BMSF-coated T25 flasks were processed for RNA extraction using methods described previously [27]. Briefly, RNA was extracted immediatelypriortothecommencementofculture(day0)andalso at day 7 and day 14 of culture. Cultured cells were treated with 1mL TRIzol reagent (Invitrogen) and then combined with chloroform (200 L/mL lysate) for 2 minutes at RT. Cellular lysates were centrifuged at 12,000 g for 15 minutes at 4∘C. Isopropyl alcohol (0.5mL/mL lysate) was added to the aqueous phase and incubated for 10 minutes at RT. After centrifugation at 12,000 g for 10 minutes at 4∘C, the supernatant was discarded and the RNA pellet washed with 1mL 75% ethanol. Subsequently, RNA pellets were centrifuged at 7,500 g for 5 minutes at 4∘C and then resuspended with 30 L ultrapure distilled water and stored at 80∘C. RNA content was estimated by spectrophotometric analysis using the ND-1000 (Thermo Scientific) spectrophotometer and A260/A280 and A260/A230 ratios calculated to estimate RNA purity.
2. 2.8.ReverseTranscription(RT). RTwasperformedbymixing 2 gsampleRNA,1 LdNTPs(125nM),1 Lrandomprimers
3. 2.9.Real-TimePolymeraseChainReaction(qPCR). Real-time PCR analysis was performed by combining 2 L sample cDNA (1:10 dilution) with 2 L forward primer and 2 L reverse primer (both 20 M, GeneWorks), 10 L SYBR green I (Roche), and 4 L ultrapure distilled water. A list of primers used in this study is shown in Table 1. The PCR reaction was initiated by incubation at 95∘C for 10 minutes. This was followed by 45 cycles of (1) 95∘C for 10 seconds, (2) 62∘C for 10 seconds, and (3) 72∘C for 10 seconds. Human beta-actin was employed as the reference gene while samples without reverse transcriptase or cDNA template were used as negative controls.

500

∗ ∗

400

HCE-T cells (mm)2

300

∗

200

100

0

Vitronectin

Fibronectin

Control

Laminin

Collagen IV

Collagen III

Collagen I

(a)

600

500

HLEcells (mm)2

400

300

200

100

0

Vitronectin

Fibronectin

Control

Laminin

Collagen IV

Collagen III

Collagen I

(b)

1. Figure 1: Adhesion of transformed HCE-T (a) or primary HLE (b) cells to BMSF coated with ECM proteins at 5 g/mL. Values represent mean SEM (HCE-T: ; HLE: ). For each cell type, an asterisk indicates that the value is significantly different ( ) from that obtained using uncoated (control) BMSF.
2. Figure 2: Morphology of HCE-T cells cultured for 1hr on fibroin coated with collagen IV at 5 g/mL (a) or uncoated (control) fibroin (b). Scale bar = 80 M.

1. 2.10. Statistical Analysis. The method of statistical analysis was two-way ANOVA. Significance level was set at and post hoc testing between treatment means was conducted using Tukey’s test.
2. 3. Results

1. 3.1. Adhesion of HCE-T and HLE Cells to ECM-Coated BMSF Films. As shown in Figure 1(a), coating of BMSF films with collagen I, collagen III, or collagen IV significantly ( ) increased the number of adherent HCE-T cells. Increased HCE-Tcelladhesionwasalsoobservedinresponsetocoating with vitronectin, fibronectin, or laminin; however, none of these increases were significantly higher ( ) than the values obtained using uncoated fibroin.

In contrast to results obtained using HCE-T cells, ECM coating had no significant effect on the adhesion of primary HLE cells to BMSF films (Figure 1(b)). Furthermore, HLE

cells exhibited a far higher tendency to adhere to uncoated fibroin than HCE-T cells. Specifically, the number of HLE cells that adhered to uncoated fibroin was approximately sixtyfold higher than that obtained using HCE-T cells (Figures

1. 1(a) and 1(b)).
2. 2(a) and 3(a)). After 25hrs of culture, however, HCE-T cells on each of the coated BMSF films demonstrated a relatively elongated morphology with eccentricity values ranging from 0.7 to 0.75 (Figure 3(a)).

0.8

HCE-T cell eccentricity value

∗ ∗ ∗

0.75

∗

0.7

0.65

0.6

0.55

0.5

Vitronectin

Laminin

Fibronectin

Control

Collagen IV

Collagen III

Collagen I

1 hour 25 hours

(a)

HLE cell eccentricity value

0.8

0.75

0.7

0.65

0.6

0.55

0.5

Vitronectin

Laminin

Fibronectin

Control

Collagen IV

Collagen III

Collagen I

1 hour 25 hours

(b)

1. Figure 3: Eccentricity of transformed HCE-T (a) or primary HLE (b) cells cultured for 1 hour or 25 hours on BMSF films coated with ECM proteins at 5 g/mL. Values represent mean + SEM (HCE-T: ; HLE: ). An asterisk indicates that the value is significantly different ( ) from the value obtained using uncoated (control) BMSF.
2. Figure4:Confluency(%)oftransformedHCE-T(a)orprimaryHLE(b)cellculturesafter1-houror72-hourgrowthonBMSFfilmspretreated with ECM proteins at 5 g/mL. Values represent mean + SEM (HCE-T: ; HLE: ). An asterisk indicates that the value is significantly different ( ) from that obtained using uncoated (control) BMSF.

In addition to the effect on cell morphology, coating of BMSF with collagen increased HCE-T culture confluence (Figure 4(a)). For example, by the end of the 72hr culture period, HCE-T cultures established on fibroin coated with collagen III or collagen IV demonstrated almost double the level of confluence exhibited by those cultures established on uncoated fibroin.

In dramatic contrast to results obtained using HCE-T cells, none of the ECM coatings had a significant effect on HLE cell morphology or culture confluence at any point during the culture period (Figures 3(b) and 4(b)).

1. 3.3. Influence of Culture Medium Characteristics on Gene Expression in HLE Cells. Messenger RNA transcripts for

p63, keratin 3, and keratin 12 were quantified by real-time quantitativePCR inHLEcellsgrownonfibroinfilmsineither SHEM medium (supplemented with Y-27632 and KGF) or DMEMfor0,7,or14days.ResultsarepresentedinTable2and Figure 5. A consistent trend observed for all donors was that culture of HLE cells in SHEM medium supplemented with Y-27632 and KGF induced much greater relative increases in the expression of keratin 3 and keratin 12 over the culture periodthanwasobservedinresponsetoculturewithDMEM. For example, after 14 days, all HLE cultures grown in SHEM medium exhibited relative increases in keratin 3 expression that were at least 30-fold higher than those observed in donor matched controls cultured in DMEM (Figure 5(a)). Similar general trends were evident when the expression of keratin

Table 2: Relative changes in gene expression in HLE cells in response to culture in different media ( ). An asterisk indicates that the value is significantly different ( ) from that obtained for the corresponding donor matched controls (DMEM).

Gene Media Days of culture dCT ddCT

7 5.95 + 0.28 0.55 + 0.28

SHEM

1. 14 5.3 + 0.16 0.93 + 0.15
2. 14 6.97 + 0.21 0.5 + 0.21

p63

7 6.72 + 1.15∗ 9.65 + 1.16∗ 14 3.67 + 0.82∗ 12.74 + 0.82∗

SHEM

Keratin 3

7 18.03 + 1.16 1.61 + 1.16 14 14.52 + 0.29 1.9 + 0.29

DMEM

7 4.79 + 0.49∗ 6.46 + 0.49∗ 14 3.03 + 0.45∗ 8.2 + 0.45∗

SHEM

Keratin 12

7 12.02 + 1.46 0.77 + 1.46 14 10.88 + 2.3 0.36 + 2.3

DMEM

20000

15000

Fold increase

10000

5000

0

7d SHEM 14d SHEM 7d DMEM 14d DMEM

(a)

600

500

400

Fold increase

300

200

100

0

7d SHEM 14d SHEM 7d DMEM 14d DMEM

(b)

Fold increase

1. 0

7d SHEM 14d SHEM 7d DMEM 14d DMEM

(c)

1. Figure 5: Fold increase in the expression of keratin 3 (a), keratin 12 (b), or p63 (c) in HLE cells from individual donors cultured in SHEM or DMEM for 7 or 14 days. Data from different treatment groups where cells were sourced from the same donor are indicated by identical fillings in individual bar graphs. Note: some values for cultures grown in DMEM in (a) and (b) are too low to register on the graph.

12 in HLE cells cultured in SHEM was compared with data obtained from donor matched control groups cultured in DMEM (Figure 5(b)).

Evidence of p63 gene expression was detected in all HLE cultures, regardless of the donor tested, the length of

the culture period, or the media used (Figure 5(c)). Overall, however, the fold change in p63 gene expression observed in response to culture with SHEM was relatively low ( 2fold) and not significantly different to that observed in donor matched groups cultured in DMEM. No significant

(a) (b)

(c) (d)

1. Figure 6: Fluorescent microscopy for p63 in HLE cells cultured on BMSF films in the presence of SHEM (a, b) or DMEM (c, d). Strong immunoreactivity (IR) for p63 was detected in all samples cultured for 7d (a, c) or 14d (b, d), regardless of the media used. No significant evidence of IR for p63 was detected in samples where primary antibody was omitted ((c), insert). Bar = 30 M.

evidence of p63 or keratin gene expression was detected in monocultures of 3T3 cells (data not shown).

1. 3.4. Influence of Culture Medium on the Expression of Specific Protein Markers in HLE Cells Grown on BMSF Films. HLE cells cultured on BMSF films in the presence of either SHEM or DMEM were investigated for the presence of p63 and keratin 3/12 by immunofluorescence at 7 and 14 days of growth. As shown in Figure 6, strong p63-IR was widely detected throughout all HLE cultures, regardless of the media used or the length of the culture period. In all instances, p63-IR was restricted to the cell nucleus. It was also noted that cells cultured in SHEM were generally smaller and present at a higher density than cells from donor matched groups cultured in DMEM. After 7 days of culture in SHEM, cytoplasmic K3/12-IR was detected in a few sparsely scattered cells throughout HLE cultures (Figure 7(a)). After 14 days of culture in SHEM, intense cytoplasmic K3/12IR was detected throughout HLE cultures from all donors examined (Figure 7(b)). By contrast, no evidence of K3/12-IR was detectable at 7 days in donor matched groups cultured in DMEM (Figure 7(c)). K3/12-IR was detected at 14 days in cultures grown in DMEM; however, the extent and intensity of this fluorescence were less than those observed in donor matched groups cultured in SHEM (Figure 7(d)).

All negative controls (omission of primary antibody) for HLE cultures failed to demonstrate any significant fluorescence (Figures 6(c) and 7(c): inserts). In addition, no

evidence of reactivity for either p63 or K3/12 was observed in monocultures of 3T3 cells (data not shown).

In previous investigations, we have shown that silk fibroin isolated from B. mori cocoons can be manufactured into flexible, permeable, and transparent scaffolds which support corneal epithelial cell attachment, growth, and differentiation [14, 15]. In the current study, we have attempted to optimize protocols for the expansion of corneal epithelial cells on BMSF in vitro by coating films with ECM proteins or including media supplements known to promote corneal differentiation and the retention of viable progenitor cell populations. In the first part of the study, it was shown that coating of fibroin films with ECM proteins, in particular collagen, significantly improved the adhesion and growth of immortalisedcornealepithelialcells(HCE-T).Thesefindings are in general agreement with those of other workers who have sought to improve protocols for the expansion of epithelial cell derived from the cornea. For example, it has been reported that coating tissue culture plastic with collagen or fibronectin significantly increases the expansion of humancornealendothelialcellcultures[18, 28–30].Likewise, collagen or laminin coating enhances corneal epithelial cell attachment and migration in vivo and promotes increased stratification on polycarbonate membranes in vitro [31, 32]. Furthermore, human corneal epithelial cells demonstrate

(a) (b)

(c) (d)

1. Figure 7: Fluorescent microscopy for keratin 3/12 in HLE cells cultured on BMSF films in the presence of SHEM (a, b) or DMEM (c, d). Keratin 3/12-IR was evident in a few sparsely scattered HLE cells in cultures grown in SHEM for 7d (a). After 14d, reactivity for keratin 3/12 was evident in all cultures regardless of the media used (b, d). No significant evidence of IR for keratin 3/12 was detected in samples cultured with DMEM for 7d (c) or where primary antibody was omitted ((c), insert). Bar = 30 M.

significantly higher rates of wound closure when cultured on therapeutic contact lenses coated with vitronectin [33]. Based on the evidence above and the response of HCE-T cells reported in the present study, we propose that coating BMSF-based scaffolds with ECM proteins may increase the potential of this biomaterial to promote increased epithelial cell adhesion and growth.

Although the finding that immortalised corneal epithelial cells demonstrate increased adhesion and growth on ECM-coated fibroin scaffolds is interesting from a scientific perspective, the potential value of this data for clinical applications is limited. In particular, the use of animal-based ECM proteins in the creation of tissue constructs for ocular surface repair or reconstruction may be problematic as it introduces potential risks associated with rejection or disease transmission. We have also demonstrated in the current study that there were major differences in the responses of immortalisedandprimarycornealcellstoECM-coatedfilms. The HCE-T cell line was selected at the commencement of the current study as a convenient and robust model system to investigate options for improving protocols for the expansion ofcornealcellculturesonBMSF-basedscaffolds.Thiscellline has often been used as a model system by other workers to gain insights into corneal epithelial cell growth or function. In particular, the HCE-T cell line has been promoted as an

alternative to the use of live animals for the study of corneal barrier function [34–36]. Nevertheless, HCE-T cells have a significantly altered genomic profile to primary corneal cells and this fact must be carefully considered when drawing conclusions on any data obtained through their use [37]. In the current study, the responses of HCE-T cells to coating fibroin films with ECM proteins were significantly different to those observed using primary HLE cells. Specifically, while HCE-T cells demonstrated increased cell attachment and growth in response to coating BMSF with ECM proteins, no such benefit was achieved for the culture of primary HLE cells. Furthermore, primary HLE cells demonstrated a much greater capacity to adhere to uncoated fibroin films than HCE-T cells and achieved much higher levels of confluence by the end of the culture period. Based on such data, we suggest that the HCE-T cell line will be only of limited value for any further attempts to optimize the expansion of HLE cells on BMSF-based scaffolds.

The second outcome of this study was that replacement of conventional keratinocyte growth media (DMEM) by medium supplemented with Y-27632 and KGF (SHEM) promoted a significant increase in corneal epithelial cell differentiation. This result is consistent with data obtained by other workers who have shown that supplementation of medium with Y-27632 and/or KGF improves epithelial cell

growth and differentiation in vivo and in vitro [38]. For example, inclusion of Y-27632 in culture medium significantly increases in the long-term proliferative capacity of primary keratinocytes from a variety of anatomical locations [39]. Supplementation of culture medium with Y-27632 also promotes increased adhesion of dissociated HLE cells apparently by protecting these cells from the stress of reactive oxygen species [40]. There is strong evidence that KGF is also a potent inducer of epithelial cell division and differentiation including those epithelial cells in the cornea and limbus. For instance, corneal epithelial wound healing is enhanced by the topical application of KGF [38, 41] while expression of the KGF receptor, FGF2bR, is significantly upregulated in the mouse corneal epithelium after scrape injury [42]. The findings of the current study indicate that the use of Y-27632 and/or KGF is also beneficial for our attempts to promote corneal differentiation in HLE cultures established on BMSFbased scaffolds.

It is important to emphasise that, in this study, increased expression of genes associated with corneal differentiation wasachievedwithoutanyapparentreductioninexpressionof the stem cell marker, p63. This outcome is highly significant since the long-term sustainability of any corneal epithelial construct requires the retention of a viable limbal progenitor population. Overall, the results of the current investigation compare favourably with those of other workers who have attempted to optimize protocols which sustain a progenitor population during HLE culture. For example, it has been shown that KGF secretion by limbal keratocytes in vivo promotes limbal epithelial cell growth and differentiation

1. [43]. Furthermore, the action of KGF on limbal epithelial cells appears to be mediated by a pathway involving the expression of p63 [44]. Evidence has also been presented that KGF-supplemented media promote the outgrowth of limbal epithelial explant cultures on amniotic membrane (AM) which express significantly higher levels of p63 than in those exposed to HGF supplemented media [44]. It has also been shown that HLE cultures which contain cells exhibiting progenitor markers can be maintained for several months in the presence of SHEM supplemented with KGF and Y27632 [23]. Based on such data, we recommend that further studies be conducted to determine whether the addition of Y27632 and KGF to culture medium helps to promote the longterm viability of progenitor populations in HLE cell cultures established on BMSF-based scaffolds.

Based on our findings, we suggest that (1) the capacity of BMSF scaffolds to support the attachment or growth of some cell types (e.g., HCE-T) may be improved by coating with ECM proteins; however, this strategy offers no significant benefit for the culture of primary HLE cells; we also suggest that (2) the use of the SHEM medium supplemented with KGF and Y-27632 in our culture system promotes increased corneal differentiation without any apparent reduction in the expression of the progenitor marker, p63. This latter finding may be of benefit for future clinical studies designed to optimize protocols for the generation of HLE constructs on

BMSF-based scaffolds for use in ocular surface reconstruction.