Corrigendum: Effects of silk fibroin in murine dry eye

Scientific Reports 7: Article number: 44364; published online: 10 March 2017; updated: 07 April 2017 This Article contains an error in the Acknowledgements section: “This study was supported by a grant from the Korea Healthcare Technology R&D Project of the Ministry of Health and Welfare Affairs, Republic of Korea (Grant No.


Results
Tear production changes of silk fibroin. Compared with the PBS groups, tear production was increased in the silk groups (Fig. 1). Tear production was decreased to 76.2% in the desiccation stress for 10 days (DS 10D) group, compared with the control, and the PBS group exhibited increased tear production (3.0-fold) at 10 days, compared with the DS 10D group (P < 0.05). However, tear production was significantly increased by 4.0fold in the 1 mg/mL and 5 mg/mL silk fibroin groups at 10 days, respectively, compared with the DS 10D group (P < 0.05). In addition, the tear volume in the 1 mg/mL and 5 mg/mL silk fibroin groups was significant increased to 1.3-fold at 10 days, compared with the PBS group (P < 0.05).
Silk fibroin induced alteration in corneal smoothness. After the desiccation stress did not change the shape of the white ring on the ocular surface in the PBS group. However, the shape of the white ring was improved on the ocular surface in the silk groups (Fig. 2a). The corneal irregularity scores were increased to 15-fold in the DS 10D group compared with the control, and a decrease to 13.3% in the PBS group was observed at 10 days compared with the DS 10D group (P < 0.05) (Fig. 2b). The corneal irregularities were decreased to 53.3% and 60% in the 1 mg/mL and 5 mg/mL silk fibroin groups at 10 days, respectively, compared with the DS 10D group (P < 0.05). Moreover, the corneal irregularities were significantly decreased to 46.2% and 53.8% at 10 days in the 1 mg/mL and 5 mg/mL silk fibroin groups, respectively, compared with the PBS group (P < 0.05).
Silk fibroin induced inhibition of epithelial cell detachment on the cornea. The corneal epithelial cells were stained with hematoxylin and eosin (H&E) (Fig. 3a). The detachment of corneal epithelial cells was increased to 16-fold in the DS 10D group compared with controls, and decreased to 93.8% in the silk groups, respectively, compared with the DS 10D group (P < 0.05) (Fig. 3b). Moreover, the detachment of corneal epithelial cells was decreased to 31.3% in the PBS group compared with the DS 10D group (P < 0.05). However, the number of detached corneal epithelial cells was significantly inhibited to 90.9% in the silk fibroin groups compared with the PBS group (P < 0.05).
Silk fibroin induced recovery of goblet cells on the conjunctiva. The goblet cells of the conjunctiva were stained with periodic acid Schiff (PAS) (Fig. 4a). The goblet cells densities of the conjunctiva decreased to 56.1% in the DS 10D group compared with the control (P < 0.05) (Fig. 4b). The goblet cell number of the conjunctiva increased to 1.7-fold and 2.1-fold in the 1 mg/mL and 5 mg/mL silk fibroin groups, respectively, compared with the DS 10D group (P < 0.05). However, the goblet cell densities of the conjunctiva increased to 1.2-fold in the PBS group compared with the DS 10D group (P < 0.05). Moreover, the densities of conjunctival goblet cells significantly increased to 1.4-fold and 1.7-fold at 10 days in the 1 mg/mL and 5 mg/mL silk fibroin groups, respectively, compared with PBS group (P < 0.05).
Anti-inflammatory effects of silk fibroin. Sections of the lacrimal gland were immunostained for TNF-α, MMP-2, MMP-9, ICAM-1, and VCAM-1 (Fig. 5a). All inflammatory factors were overexpressed in the DS 10D group compared with the controls (Fig. 5b). The number of stained TNF-α cells decreased by 80% in the silk groups, compared with the DS 10D group (P < 0.05). Staining for ICAM-1 was decreased by 71.4% and 82.1% in the silk groups, respectively, compared with the DS 10D group (P < 0.05). The stained VCAM-1 cells were inhibited by 65% and 85% in the silk groups, respectively, compared with the DS 10D group (P < 0.05). MMP-2 expression was decreased by 76.9% and 84.6% in the silk groups, respectively, compared with the DS 10D group (P < 0.05). The stained MMP-9 cells were inhibited by 70.8% and 87.5% in the silk groups, respectively, compared with the DS 10D group (P < 0.05). However, all inflammatory factors exhibited no significant decrease in the PBS group compared with the DS 10D group. Moreover, the expression of ICAM-1, VCAM-1, MMP-2 and MMP-9 was reduced by 37.5%, 57.1%, 33.3% and 57.1% in the 5 mg/mL silk fibroin groups, respectively, compared with the 1 mg/mL silk fibroin group (P < 0.05).

Discussion
We confirmed the efficacy of silk fibroin in our experimental mouse model of dry eye. The silk fibroin exhibited increased tear production and reduced irregularity score of ocular surface in the dry eye. In addition, silk fibroin Most dry eye treatments such as cyclosporine A, topical corticosteroids, tetracyclines, macrolides, and omega-3 and omega-6 fatty acids are known [12][13][14][15][16][17][18][19][20][21] . Cyclosporine and corticosteroids are anti-inflammatory agents that regulate the pro-inflammatory cytokines in the conjunctiva and lacrimal glands. Topical cyclosporine has been reported to improve tear production, decrease apoptosis of the corneal epithelial cells, and increase the number of conjunctival goblet cells through the inhibition of T-cell activation. However, cyclosporine appears to cause eye pain, irritation, and soreness symptoms in patients with dry eye, and long-term use of corticosteroids leads to side effects 22 . Tetracyclines and macrolides are antibiotics, which do not have an observed direct anti-inflammatory effect in dry eye. In addition, omega-3 and omega-6 fatty acids are unsaturated fatty acids, which help to supplement the lipid layer of tear film.
In a previous study, we investigated the a study on the effects of a therapeutic candidate agent in dry eye; we observed the effects of quercetin and chondrocyte-derived extracellular matrix in murine dry eye 5,6 . Quercetin is one of the flavonoid known to have antioxidant and anti-inflammatory effects; it decreased the detached epithelial cells of the cornea, reduced the number of conjunctival goblet cells, and exhibited anti-inflammatory effects in the lacrimal gland 5 . Chondrocyte-derived extracellular matrix is a new therapeutic agent that has demonstrated significantly suppressed neovascularization in a rabbit model of alkaline burn rabbit model and a pterygium mouse model as well as reduced the induction of inflammatory factors from the cornea or conjunctiva of a mouse model of dry eye 6,43,44 . Silk is known to be useful in slowing tissue ingrowth into the biomaterial scaffold in vivo and in vitro, because of the slow rates of degradation [27][28][29][30] . In addition, there has been active research on the various formulations and preparation methods of the silk [31][32][33] . Silk has been studied in a variety of fields, such as bone tissue reconstruction, fabrication of artificial skin, acute tympanic membrane perforation, scaffolds for artificial esophagus, and segmental defects of the zygomatic arch [45][46][47][48][49][50] . In particular, silk membranes are suitable as a substrate for the restoration of damaged ocular surfaces to promote cellular attachment and growth in human limbal epithelial cells 34,35 .  Dry eye has been reported to cause inflammation, as well as abnormality of the cornea and conjunctiva from destabilization of the tear film, such as the lipid layer, aqueous layer, and mucous layer on the ocular surface [3][4][5][6][7][8][9][10][11] . These results suggest that the silk fibroin recovered the aqueous layer of tear film through its anti-inflammatory effects in the lacrimal gland and improved the mucus layer of tear film by increasing the number of conjunctival goblet cells in our experimental mouse model of dry eye. In addition, this improved tear film inhibited corneal epithelial damage, contributing to increased tear volume and improvement of ocular surface irregularity by the dry eye. This indicates that the silk fibroin provided a good environment through tear film stabilization in the ocular surface of the dry eye, which resulted in the recovery of the cornea, conjunctiva, and lacrimal gland of the dry eye.
In conclusion, our study demonstrated that silk fibroin has multi-target therapeutic effects that regulate inflammation of the lacrimal gland as well as ameliorate corneal and conjunctival abnormalities such as decreased tear production, deterioration of ocular surface smoothness, detachment of corneal epithelial cells and reduction of number of conjunctival goblet cells in dry eye. Therefore, silk fibroin is a potential new drug with great efficacy for treating inflammation and stabilizating the tear film in dry eye disease.

Preparation of silk fibroin solution.
Silk fibroin aqueous solution was derived from B. mori cocoons. The procedure for the preparation of a silk solution is normally comprises three steps. The first process is a degumming step. Cocoons were finely chopped and boiled in 0.02 M sodium carbonate (Na 2 CO 3 ) for an hour to be degummed. The silk fibers were then washed with distilled water and dried. The extracted silk fibroin was then dissolved in a mixing solution (CaCl 2 : Ethanol: H 2 O = 1: 2: 8) at 98 °C for 1 hour, yielding a 15 W/V% solution. This solution was dialyzed in distilled water using a dialysis membrane (MWCO 12,000-14,000, Spectra/Por, Spectrum Labs, Rancho Dominguez, CA) for 3 days. The concentration of the silk fibroin solution was calculated to 6 wt%. In this study, final silk fibroin solution was diluted to 0.1% (1 mg/mL) and 0.5% (5 mg/mL). The silk fibroin solutions were then stored at 4 °C before use to avoid premature precipitation 51  Experimental procedures of murine dry eye. Desiccation stress was created by low ambient humidity (30-40%) using an air draft from a fan for 18 hours per day, and 0.5 mg/0.2 mL hypodermic injection of scopolamine hydrobromide (Sigma-Aldrich, St. Louis, MO) into both hindquarters (one after the other) four times (9 AM, 12 PM, 3 PM, and 6 PM) per day for 10 days on more than 12-weeks-old male NOD.B10.H2 b mice 52,53 . After the desiccation stress for 10 days, the scopolamine hydrobromide injections were discontinued and the mice were placed in an environment of normal humidity and temperature. The eye drops, PBS and 1 mg/mL or 5 mg/ mL silk fibroin were administered five times (9 AM, 11 AM, 1 PM, 3 PM, and 5 PM) per day for 10 days (Fig. 6).
The experiment was divided into the following groups: control (normal, n = 5); DS 10D (untreated, desiccation stress for 10 days, n = 5); PBS (n = 5, 10 μL treated PBS in both eyes after the desiccation stress); silk fibroin 1 mg/ mL (n = 5, 10 μL treated 1 mg/mL silk fibroin in both eyes after the desiccation stress); and silk fibroin 5 mg/mL (n = 5, 10 μL treated 5 mg/mL silk fibroin in both eyes after the desiccation stress). Mice in all groups were euthanized after the treatment period. Tear production measurements. Measurement of tear volume was performed using phenol red-impregnated cotton threads (Zone-Quick; Oasis, Glendora, CA), as previously described 54 . The threads were put in the lateral canthus of mice using a forceps for 20 seconds. The threads that absorb tears changed to red, and the red threads were evaluated in a millimeter through a microscope (SZX7; Olympus Corp., Tokyo, Japan). The tear volume was converted from millimeter to microliter compared with a standard curve 55,56 . The tear volume was measured within 2 hours of the scopolamine injection and within 1 hour of the PBS or silk fibroin administration, and evaluated by the average value from both eyes 5,6 . Measurement of the corneal smoothness and irregularity score. The corneal smoothness was measured after the euthanization of the mice, to obtain an image of the white ring under a fiber optic ring illuminator from a stereoscopic zoom microscope 6 . The smoothness of the cornea was measured within 2 hours of the scopolamine injection and within 1 hour of the PBS or silk fibroin administration, and evaluated by the average value from both eyes 5,6 . The corneal irregularity was evaluated by scoring the reflected distortion of the white ring of the epithelium of the cornea in the digital image, as previously described 15 . The irregularity scores of the cornea were evaluated according to the distorted quarters of the reflected ring, according to a five-point scale as follows: 0, no distortion; 1, 1/4 distortion; 2, 1/2 distortion; 3, 3/4 distortion; 4, 4/4 distortion; and 5, severe distortion and the shape of the ring is not recognized.
Histologic experiment. The eyes and adnexa of each groups were surgically extraction, and then fixed by 10% formalin. The fixed tissues were embedded using paraffin and optimal cutting temperature compound (Tissue-Tek, Sakura Fine Technical Co., Ltd., Tokyo, Japan). The embedded tissues were sectioned to 6 μm, and then H&E and PAS staining was performed. The sections of each group were evaluated oven a range of 0.1 mm 2 in the cornea and inferior fornices of the conjunctiva. The stained slides of each group were imaged through a Virtual Microscope (NanoZoomer 2.0 RS, Hamamatsu, Japan). The detachment of corneal epithelial cells and density of conjunctival goblet cells were evaluated as the average value of three non-consecutive cross-section slides from four mice per group.
Immunohistochemistry. The eyes and adnexa were surgically excised, embedded in optimal cutting temperature compound, and flash frozen in liquid nitrogen. Six micrometer sections were excised with a cryostat. The sections were fixed with pre-cooled acetone for 5 minutes, and the primary antibodies to TNF-α (Abcam Inc., Cambridge, MA), MMP-2 (Abcam Inc., Cambridge, MA), MMP-9 (Lifespan Biosciences Inc., Seattle, WA), ICAM-1 (Bioss Inc., Woburn, MA), and VCAM-1 (Bioss Inc., Woburn, MA) were added and incubated for 1 hour at room temperature. After washing, the sections were incubated with secondary antibody (DAKO Corp, Glostrup, Denmark) for 30 minutes. Immunoreactions were visualized with diaminobenzidine chromogen, and the sections were counterstained with Mayer's hematoxylin (Sigma-Aldrich) for 30 seconds at room temperature. Images of the sections were photographed with a Virtual Microscope (NanoZoomer 2.0 RS). The stained cells were evaluated oven a range of 0.1 mm 2 in the lacrimal gland of each group. Statistical analysis. All data were analyzed using SPSS version 18.0 (SPSS, Chicago, IL) for Windows and reported as mean ± standard deviation. The comparative analysis of differences between groups were performed by two-way analyses of variance (with Tukey's test), and statistical significance was indicated by P < 0.05.