Background To develop targeted antifibrotic therapy for glaucoma filtration surgery; this study determines the effectiveness of small interfering RNA (siRNA) to reduce in vivo secreted protein acidic and rich in cysteine (SPARC) expression using the mouse model of conjunctival scarring.
Methods Experimental surgery was performed as described for the mouse model of conjunctival scarring. Scrambled (siScram) or Sparc (siSparc) siRNAs, loaded on layer-by-layer (LbL) nanoparticles, were injected into the conjunctiva immediately after surgery. Expression of Sparc, Col1a1, Fn1 and Mmp14 was measured by real-time PCR and immunoblotting on days 7 and 14 postsurgery. Live imaging of the operated eyes was performed using slit lamp, anterior segment-optical coherence tomography and confocal microscopy. Tissue pathology was evaluated by histochemical and immunofluorescent analyses of operated conjunctival cryosections. Tissue apoptosis was quantitated by annexin V assay.
Results siSparc, delivered via expanded LbL nanoparticles, significantly inhibited Sparc transcription in both day 7 (2.04-fold) and day 14 (1.39-fold) treated tissues. Sparc suppression on day 7 was associated with a significant reduction of Col1a1 (2.52-fold), Fn1 (2.89-fold) and Mmp14 (2.23-fold) mRNAs. At the protein level, both SPARC and collagen 1A1 (COL1A1) were significantly reduced at both time points with siSparc treatment. Nanoparticles were visualised within cell-like structures by confocal microscopy, while overt tissue response or apoptosis was not observed.
Conclusions SPARC targeted therapy effectively reduced both SPARC and collagen production in the operated mouse conjunctiva. This proof-of-concept study suggests that targeted treatment of fibrosis in glaucoma surgery is safe and feasible, with the potential to extend to a range of potential genes associated with fibrosis.
- treatment surgery
- wound healing
- Experimental – animal models
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The major benefits of targeted therapy include reduced adverse effects on unaffected tissues and the promise of increased effectiveness in achieving the therapeutic goal. Precise knowledge of the molecular pathways being modulated also allows for accurate evaluation of therapeutic effectiveness and efficiency and facilitates improved therapeutic strategies with other synergistic/combinatorial treatments. Moreover, individualised treatment is possible based on the unique genetic predisposition of each patient.
In glaucoma filtration surgery (GFS), subconjunctival fibrosis over the sclerostomy site occurs to varying degrees and is a major cause of surgical failure.1 Antiscarring agents are routinely applied as surgical adjuncts to reduce the fibroproliferative response and improve the success rates of the surgery. For this purpose, mitomycin C (MMC) is the most commonly used adjunct. Although MMC is highly effective in reducing the postoperative scarring response, surgeries continue to fail.2 Moreover, its non-specific and irreversible properties increase the rate of sight-threatening complications including infection and hypotony.3 Furthermore, some patients appear to develop resistance to MMC treatment.4 Hence, fibrosis in GFS is a condition that may benefit greatly from targeted therapy, either alone or in conjunction with current antifibrotic therapy to overcome drug resistance and/or reduce adverse side effects.
In this study, we explore the feasibility of a targeted approach to antifibrotic therapy for the operated conjunctiva via small interfering RNA (siRNA). The target gene is the 32 kDa, secreted protein acidic and rich in cysteine (SPARC), also known as osteonectin and BM-40. SPARC is a prototypic calcium-binding matricellular protein.5 Matricellular proteins are secreted glycoproteins that are largely non-structural and involved in mediating cellular interactions with components of the extracellular matrix (ECM).6 SPARC is conspicuously induced at sites of wound healing and tissue remodelling, including the wounded conjunctiva.7 Conversely, when SPARC is absent, as in the SPARC knockout mouse, altered collagen fibrillogenesis and delayed fibrosis was observed.8 Indeed, we have also found that SPARC−/− mice displayed reduced fibrosis in the mouse model of conjunctival scarring.9 A likely mechanism for this antifibrotic response is the reduced deposition of collagen which was assembled from collagen fibrils that were thinner than normal.9 We have since confirmed that collagen expression and fibril thickness in the SPARC-null mouse is also significantly lower than normal in other parts of the eye, such as the iris.10 Although collagen is thought to be the key protein regulated by SPARC,11 loss of SPARC was also associated with reduced deposition of other extracellular matrix components such as fibronectin (FN) and matrix metalloproteinases (MMP-2 and MMP-14) in the operated conjunctiva.9 All these data support the targeting of SPARC expression as a means to reduce deposition of collagen and other extracellular matrix proteins and is therefore a potential antifibrotic therapeutic strategy.
We have previously established that Sparc expression was amenable to silencing by small interfering RNA (siRNA) in primary mouse conjunctival fibroblasts and this inhibition was associated with reduced collagen expression.12 As a method for siRNA delivery, we have shown that layer-by-layer (LbL) nanoparticles comprising of poly-L-arginine (ARG) atop a hydroxyapatite (HA) core successfully silenced Sparc expression in conjunctival fibroblasts.13 In this study, we further demonstrate that treatment with Sparc siRNA-loaded LbL nanoparticles in the mouse model of conjunctival scarring effectively reduced production of SPARC and extracellular matrix proteins, particularly collagen. While SPARC and collagen suppression remained effective for at least 2 weeks post-treatment, the control of other extracellular proteins including FN and MMP-14 was effective mainly in the short term. Finally, we did not find apparent tissue toxicity or tissue response in the operated mouse conjunctiva treated with the siRNA-loaded nanoparticles. Overall, our data suggest that genetic inhibition by means of siRNA-based gene silencing is a promising targeted strategy for ameliorating conjunctival fibrosis after GFS.
Materials and methods
Mouse model of conjunctival scarring
All experiments with animals were treated in accordance with the Association for Research in Vision and Ophthalmology (ARVO) Statement on the Use of Animals in Ophthalmic and Vision Research. Wild type C57BL6/J mice, bred and maintained at the Department of Experimental Surgery (Singapore General Hospital, Singapore), were used. Experimental surgery, resulting in conjunctival scarring, was performed on the left eye of each mouse to induce scarring as described previously.9 Mice were anaesthetised by intraperitoneal injection of a 0.1 mL ketamine/xylazine mixture containing 2 mg/mL xalazine hydrochloride (Troy Laboratories, Smith-field, Australia) and 20 mg/mL ketamine hydrochloride (Ketamine, Parnell Laboratories, Alexandria, Australia) as well as topically with one drop of 1% xylocaine per eye before surgery was performed. The conjunctiva was surgically dissected to expose the underlying sclera, after which an incision was made through the sclera into the anterior chamber of the eye with a 30-gauge needle to create a fistula. The wound was then secured and closed at the limbus by a 10–0 (0.2 metric) Ethilon black monofilament nylon scleral suture (Ethicon). LbL nanoparticles in 5 µL phosphate-buffered saline (PBS), loaded with either scrambled or Sparc siRNA, were administered by direct injection into the conjunctiva at the surgical site immediately after surgery. Fucithalmic ointment (Leo Pharmaceutical Products, Ballerup, Denmark) was instilled at the end of the procedure to prevent infection. For molecular evaluation of tissues on days 7 or 14 after surgery, mice were euthanised by intraperitoneal injection of pentobarbitol sodium, at 100 mg/kg body weight, before conjunctival tissues were harvested.
The siRNAs used in this study were: scrambled control siRNA 5′-GCUCACAGCUCAAUCCUAAUC-3′, Sparc siRNA 5′-AACAAGACCUUCGACUCUUCC-3′. These siRNAs were custom synthesised and purchased from Bioneer Corp. (South Korea).
Preparation of siRNA LbL nanoparticles
The LbL nanoparticle fabrication was performed as described previously.13 HA nanoparticles at 10 mg/mL was added to ARG solution at 0.5 mg/mL, in a volume ratio of 1:10, with maximum vortex mixing and light sonication for 10 min. The ARG-coated nanoparticles were suspended in 0.1 M NaCl and mixed with 1.2 pmol of siRNA per µg HA for 1 hour. Another layer of ARG was added by mixing with the 0.5 mg/mL ARG solution. This method will generate the three-layer configuration (HA-ARG-siRNA-ARG).13 To obtain the five-layer configuration (HA-ARG-siRNA-ARG-siRNA-ARG), the above coating steps were repeated with 1.2 pmol of siRNA per µg HA and ending with a final layer of ARG. The nanoparticles were resuspended in sterile PBS and stored at 4˚C before use. LbL nanoparticles loaded with siScram are labelled as siScram-LbL while those loaded with siSparc are labelled as siSparc-LbL in the text and figure legends.
Real-time quantitative PCR (qPCR) analysis
Operated conjunctival tissues injected with siRNA-loaded nanoparticles from five mice were pooled as one group in a total of five groups for each condition (n=5). Tissues from the contralateral untreated eyes in each group of mice were similarly pooled and used as baseline for calculation of fold change in mRNA expression in each group. Conjunctival tissues were processed and analysed by qPCR as described previously.7 All qPCR reactions were performed in triplicate. All mRNA levels were measured as CT threshold levels. Rpl13a was the used as the housekeeping gene for days 7 and 14 operated conjunctival tissues injected with the siRNA-loaded LbL nanoparticles. Values were calculated as fold changes relative to similarly pooled contralateral, unoperated conjunctival tissues by the 2-∆∆CT method. The primers used were as follows: Rpl13a-forward 5′-GAGGTCGGGTGGAAGTACCA-3′ and Rpl13a-reverse 5′-TGCATCTTGGCCTTTTCCTT-3′; Sparc-forward 5′-AAACATGGCAAGGTGTGTCA-3′ and Sparc-reverse 5′-AAGTGGCAGGAAGAGTCGAA-3′; Col1a1-forward 5′-CCCACCCCAGCCGCAAAGAG-3′ and Col1a1-reverse 5′-GCCATGCGTCAGGAGGGCAG-3′; Fn1-forward 5′- ATGTGGACCCCTCCTGATAGT-3′ and Fn1-reverse 5′-GCCCAGTGATTTCAGCAAAGG-3′; Mmp14-forward 5′-TGGCATCCAGCAACTTTATG-3′ and Mmp14-reverse 5′-TTTGGGCTTATCTGGGACAG-3′.
Operated conjunctival tissues from mice treated with siRNA-loaded nanoparticles were harvested after 7 or 14 days and processed as described previously.7 Operated conjunctival tissues from five mice were pooled as one group in a total of three groups for each condition (n=3). Antibodies against SPARC, collagen 1A1 (COL1A1), FN1, MMP-14 and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) were purchased from Cell Signalling Technology (Massachusetts, USA), Abnova Corp. (Colorado, USA), Epitomics (Abcam, Massachusetts, USA), Abcam (Massachusetts, USA) and Santa Cruz Biotechnology (California, USA), respectively. Horseradish peroxidase-conjugated secondary antibodies were from Jackson ImmunoResearch Laboratories (Pennsylvania, USA). Densitometric quantitation was performed using Image Studio Lite V.5 (LI-COR Biosciences, Nevada, USA). Normalisation to correct for variations in loading was performed using GAPDH as the housekeeping protein.
In vivo imaging of mouse eyes
Operated mice were anaesthetised by intraperitoneal injection of a 0.1 mL ketamine/xylazine mixture containing 2 mg/mL xalazine hydrochloride (Troy Laboratories, Smith-field, Australia) and 20 mg/mL ketamine hydrochloride (Ketamine) before imaging was performed. Slit-lamp microscopy was performed using Righton LED slit lamp MW50D (Right Mfg Co Ltd, Japan). Anterior segment-optical coherence tomography (AS-OCT) was carried out using the Optovue RTVue100-2 Fourier domain optical coherence tomography system (Optovue, California, USA). In vivo confocal microscopic examinations of the operated and treated conjunctiva were performed using Hrt3 microscope (Heidelberg Engineering, Heidelberg, Germany).
Histochemical and immunofluorescent evaluation of cryosections
Histochemical evaluation of operated conjunctival cryosections by H&E or picrosirius red staining was performed as described previously.7 Polarisation microscopy was performed using the Nikon Eclipse Ti microscope (Nikon Instruments, New York, USA). For immunofluorescent analyses, labelling by primary antibodies for SPARC (sc59703; Santa Cruz Biotechnology), COL1A1 (H00001277-M01; Abnova, Taiwan), FN1 (1574–1; Epitomics/Abcam) or MMP-2 (250752; Abbiotec, California, USA) was detected using secondary goat antibodies conjugated to Alexa Fluor-488 (A11001; green fluorescence) or Alexa Fluor-594 (A11012; red fluorescence), both obtained from Invitrogen Corp. (Thermo Fisher Scientific, Massachusetts, USA). Nuclei were visualised by mounting the cells in 4′,6-diamidino-2-phenylindole-containing Vectashield mounting medium (Vector Laboratories, California, USA). Labelled cells were visualised using the Zeiss Imager.Z1 microscope (Carl Zeiss, USA).
Annexin V assay by flow cytometry
Apoptosis in the operated conjunctival tissues was measured using the Guava Nexin Reagent (Guava Technologies, Hayward, California, USA) by flow cytometry according to manufacturer’s instructions. Cells were isolated for flow cytometry as described previously.7 Five thousand cells were analysed for each sample in a total of five samples for each condition (n=5). Cell populations were quantified using the Guava Nexin software (EMD Millipore, Massachusetts, USA).
Data are expressed as mean±SD. For pairwise comparison of fold mRNA or protein expression between siScram-LbL and siSparc-LbL treated tissues, the significance of differences between the two conditions was determined by the two-tailed Student’s t-test. For comparison of %Annexin V+cells in tissues between different treatment conditions, the significance of differences between the time points or treatments was determined by one-way analysis of variance with Bonferroni post-hoc adjustment using SPSS statistics. A p value of <0.05 was deemed to be significant.
Downregulation of SPARC and extracellular matrix molecules in the operated conjunctiva treated with siSparc-loaded nanoparticles
We have previously shown that LbL nanoparticles containing one layer of Sparc siRNA (siSparc) was effective in silencing Sparc expression in cultured conjunctival fibroblasts.13 Hence, we first determined whether nanoparticles in this three-layered format was effective for delivering Sparc silencing in the mouse model of conjunctival scarring after 7 days of treatment. The three-layered LbL nanoparticles were 275±2 nm in hydrodynamic diameter with a surface charge of 47±5 mV and polydispersity of 0.26±0.02 (data not shown). These particles consisted of 1.2 pmol of siRNA per µg HA/siRNA layer, enabling the injection of 3208 ng siRNA per mouse eye. When compared with tissues injected with scrambled siRNA (siScram), tissues treated with siSparc demonstrated no significant alteration of either Sparc or Col1a1 mRNA expression (data not shown). These data suggest that the three-layered nanoparticles did not have the capacity to deliver specific Sparc silencing through their siRNA payload in the operated conjunctiva.
To investigate whether greater quantities of siRNA may be required to bring about Sparc silencing in vivo, we fabricated five-layered LbL nanoparticles containing an additional layer of siSparc (figure 1A). The five-layered LbL nanoparticles were 242±2 nm in hydrodynamic diameter with a surface charge of 49.3±0.8 mV and polydispersity of 0.19±0.02. These particles also consisted of 1.2 pmol of siRNA per µg HA/siRNA layer, but with the incorporation of an additional layer of siRNA, we were able to inject 6417 ng siRNA per mouse eye.
Treatment of the eyes with nanoparticles containing the enhanced siRNA load for 7 days effectively reduced Sparc mRNA levels by mean 2.04-fold (p=0.0038) compared with the scrambled controls (figure 1B). Importantly, decrease in Sparc mRNA expression was associated with significant reduction in Col1a1 transcript expression by mean 2.52-fold (p=0.00034) relative to scramble controls. Fn1 and Mmp14 transcripts were also significantly reduced by 2.89-fold (p=0.0081) and 2.23-fold (p=0.029), respectively, in the siSparc-treated tissues (figure 1B). We further determined that siSparc treatment also resulted in reduction of Sparc transcript expression on day 14 postsurgery (figure 1C). At this latter time point, Sparc transcript levels remained significantly reduced by 1.39-fold (p=0.049). However, there was no corresponding reduction of Col1a1, Fn1 or Mmp14 mRNA expression on day 14 (figure 1C).
At the protein level, both SPARC and COL1A1 were significantly and consistently reduced in tissues treated with siSparc (figure 2). After 7 and 14 days, SPARC protein levels were reduced by mean 1.41-fold (p=0.044) (figure 2A) and 1.89-fold (p=0.049) (figure 2B), respectively. COL1A1 protein was also reduced by mean 2.34-fold (p=0.014) and 2.41-fold (p=0.017) on treatment with siSparc-loaded nanoparticles for 7 and 14 days, respectively. On the other hand, FN1 was only significantly reduced in tissues 7 days after treatment with siSparc, while in the extended period of 14 days, FN1 was no longer suppressed (figure 2A,B). MMP-14 protein levels were not significantly altered by siSparc treatment at both time points. Collectively, these data indicate that siRNA delivered via expanded LbL nanoparticles has the capacity to effectively suppress target (SPARC) and closely associated downstream target (COL1A1) expression for at least 14 days in vivo, while the impact on other indirect targets, including FN1 and MMP14, was less effective.
Imaging the operated conjunctiva treated with siRNA-loaded nanoparticles
To visualise the tissue response to LbL nanoparticle-facilitated siRNA treatment, we imaged the live, operated mouse conjunctiva on days 0, 2, 7 and 14 after injection with either siScram-loaded or siSparc-loaded nanoparticles (figure 3). The injected nanoparticles were conspicuous as a white amorphous substance comprising coalesced nanoparticles when visualised by both slit-lamp microscopy and AS-OCT. Slit-lamp microscopy revealed no overt local conjunctival tissue reaction or increased vascularity beyond what is normally observed as a result of the surgery per se at any of the indicated time points. AS-OCT also did not show any segregation of the surrounding conjunctival tissue from the optically dense nanoparticle material, suggesting that the nanoparticles were well tolerated in the treated tissue. In confocal images, the nanoparticles were observable at first as undefined, large, opaque masses immediately postinjection (day 0) and as dense white specks or lumps in the tissue as they scattered at later times. Interestingly, the nanoparticles can be visualised within numerous cell-like structures from day 2 and remained visible in these structures on day 14 postsurgery (red arrowheads and insets, figure 3). These observations suggest that the nanoparticles, loaded with siRNAs, were taken up and retained by cells in the treated tissue for at least 2 weeks, providing support for the capacity of these nanoparticles to successfully deliver siRNA into the cells.
Histochemical evaluation of the day 14 operated conjunctiva treated with siRNA-loaded nanoparticles
We further investigated whether a foreign body reaction may have developed against the siRNA-loaded LbL nanoparticles by examining the treated tissue pathology. In corroboration with the live imaging observations above, overt tissue reaction was not observed in the histological sections of the operated conjunctivas treated with nanoparticles loaded with either scrambled or Sparc siRNAs for 14 days (figure 4A). The LbL nanoparticles appeared as relatively small patches of coalesced particles with intense absorption of the histological dyes (figure 4A, arrowheads). At higher magnification, LbL nanoparticles loaded with siScram seemed to be surrounded by darker-staining fibres (figure 4B, arrowheads). In comparison, we did not detect such fibres around a similarly sized patch of aggregated siSparc-loaded LbL nanoparticles (figure 4B). Histochemical staining of the operated and treated conjunctiva with picrosirius red revealed a similar overall tissue appearance (figure 4C). As before, the LbL nanoparticles were conspicuous as they were also saturated with this collagen-staining dye (figure 4C, arrowheads). Notably, collagen fibres seemed to penetrate the area containing LbL nanoparticles normally, suggesting that the nanoparticles did not perturb the restoration of the collagen matrix during wound healing. Moreover, the nanoparticles appeared to have settled on collagen fibres which may serve as scaffolds for stable deposition. These observations suggest that treatment with siRNA-loaded LbL nanoparticles did not provoke an overt foreign body or tissue response in the operated conjunctiva and allow normal matrix reformation, properties which are beneficial towards in vivo application in targeted therapy.
Immunofluorescence evaluation of the day 14 operated conjunctival extracellular matrix treated with siRNA-loaded nanoparticles
We also examined the operated conjunctival extracellular matrix by immunofluorescence analyses. As before, the LbL nanoparticles in the cryosections were readily visualised as patches of coalesced particles of varying sizes under brightfield microscopy (figure 5). Immunostaining for SPARC revealed conspicuously fewer positive staining areas in the operated conjunctiva treated with siSparc than that treated with siScram (figure 5A), confirming the reduction of SPARC protein expression with this treatment. Fewer COL1A1-positive staining areas may also be observed with siSparc treatment, although less obvious (figure 5B). At higher magnification, a patch of aggregated siScram-loaded LbL nanoparticles can be visualised to be surrounded by COL1A1 (figure 5B, left, inset), suggesting fibrotic encapsulation of the coalesced nanoparticles. In comparison, a patch of coalesced siSparc-loaded LbL nanoparticles contained less enveloping COL1A1 (figure 5B, right, inset). The distribution of FN1 (figure 5C) and MMP-2 (figure 5D) did not appear to be obviously different between the two treatments. These observations confirmed that siSparc treatment maintained conspicuously less SPARC deposition in the conjunctiva 14 days after experimental surgery. Moreover, siSparc treatment may also be advantageous for controlling collagen encapsulation of the delivery nanoparticles.
Toxicity evaluation of the operated conjunctiva treated with siRNA-loaded nanoparticles
To evaluate long-term tissue toxicity of Sparc silencing, apoptotic cells in day 14 operated conjunctival tissues were quantitated by flow cytometry (figure 6). Compared with the experimental surgery alone, the injection of nanoparticles loaded with either scrambled or Sparc siRNAs did not significantly increase the number of annexin V-positive cells (p>0.05, figure 6) or cause loss of overall cell viability (p>0.05, figure 5). Moreover, specific treatment with siSparc did not induce significant apoptosis or change the level of cellular viability in the operated conjunctivas compared with treatment with scramble siRNA (p>0.05). Hence, targeting Sparc expression in the mouse conjunctiva is a safe antifibrotic therapeutic strategy.
This study demonstrates that effective downregulation of a specific gene in the postoperative conjunctiva, in association with its downstream targets, can be achieved via siRNA. Furthermore, our data show that targeted therapy via siRNA loaded on nanoparticles did not cause tissue cell death or overt adverse tissue responses. This proof-of-concept study supports the application of genetic inhibition as effective and safe targeted therapy for treating fibrosis post-GFS.
In this study, we opted to investigate SPARC as the molecule of interest. SPARC has the attributes of a bona fide target molecule for antifibrotic therapeutic development. First of all, SPARC expression features prominently in tissues undergoing turnover such as during development, wound healing and in diseased states, particularly fibrosis.14–20 We have also observed increased SPARC expression in the mouse model of conjunctival scarring.7 The specific induction of SPARC in activated tissues implies that this molecule may not be critical for normal tissue function in the steady state but is required when tissue turnover occurs. Hence, reducing SPARC expression is not expected to have adverse effects on normal tissues.
Second, SPARC is an ECM-modulatory molecule, being conspicuously involved in the regulation of collagen deposition, both quantitatively and qualitatively in terms of fibril characteristics.11 In fact, the ability of SPARC to bind collagen as well as modulate its production and assembly is believed to be key to its functional properties.21 It is speculated to behave as a collagen chaperone to ensure that only correctly folded procollagen molecules exit the cell.22 As proof of its collagen-regulatory activity, SPARC deficiency is associated with defective ECM architecture and composition.23–26 We have also previously reported that SPARC deficiency resulted in altered collagen fibrillogenesis in the eye9 10 and delayed fibrosis during wound healing.9 Thus, SPARC is strongly implicated as a protein involved in mediating fibrosis by regulating collagen production and assembly in the ECM.27 This knowledge is critical to the evaluation of Sparc silencing as a successful therapeutic approach. We were able to confirm that SPARC siRNA effectively inhibited SPARC expression (primary target) in the treated conjunctiva, as well as demonstrate the concomitant suppression of collagen as its major downstream, indirect target. The pathology of the siSparc-treated operated conjunctivas was especially revealing in showing reduced accumulation of not only SPARC but also lesser collagen fibres encapsulating the coalesced nanoparticle patches. These data therefore strongly support the specificity, effectiveness and efficiency of this therapeutic system.
Although we have previously demonstrated successful gene silencing using LbL nanoparticles as nanocarriers for siRNA in vitro,13 we found in this study that expansion of the LbL format was required to deliver sufficient siRNA in vivo for effective gene silencing. The addition of two more layers did not dramatically alter the hydrodynamic size of the nanoparticles, nor did it impede their accumulation in cell-like structures or caused an overt tissue response in the conjunctiva. The slit-lamp images initially indicated that the nanoparticles were mainly confined in the tissue as a single large mass in the early days post-treatment, but they appeared to progressively scatter with time. Indeed, histological examination revealed aggregated nanoparticles distributed in localised patches of uneven sizes throughout the 14-day operated conjunctiva. This pattern of distribution into smaller parts probably prevented the development of a large-scale foreign body reaction as some tissue reaction on a small scale, in the form of collagen fibres enveloping some patches of coalesced nanoparticle, was certainly observed. The suppression of collagen deposition by siSparc is particularly advantageous in this respect since the formation of collagen encapsulation appeared to be repressed, which in turn may enhance the effectiveness of the delivery vehicle. Moreover, the aggregated patches may help preserve the integrity of the siRNA within and so help prolong the lifespan of the gene silencing effects. Hence, the primary reasons driving the in vivo Sparc silencing effectiveness may be attributed to increased quantity of siRNA being delivered to the conjunctiva with the expanded LbL nanoparticle format and to subdued tissue reaction and/or protection of siRNA facilitated by the distribution of the nanoparticles in small coalesced patches.
The capacity of the nanoparticle system to achieve sustained gene downregulation in the conjunctiva has a clear advantage in that multiple injections of these siRNA-loaded drugs are potentially not required to maintain the therapeutic effect for an extended period of time postsurgery. However, there was an apparent reduction in efficiency of gene silencing with time, which we presume to be related to depletion and/or loss of siRNA stability in the tissue. The lower efficiency of Sparc silencing at the later time point was associated with loss of significant reduction in Col1a1 transcription, implying that a minimum threshold delivery of siRNA or Sparc silencing was required to generate a significant downstream effect. The same may be said for regulation of the other extracellular matrix genes, Fn1 and Mmp14, which were also suppressed by SPARC inhibition at the mRNA level in the short term, but their regulation at the protein level, and in the extended period post-treatment, appeared to be less effective. Hence, the capacity to deliver large quantities of siRNA, and for a prolonged period, is clearly a factor that needs to be considered in future designs of siRNA delivery systems. Nevertheless, our data indicate that active target gene silencing is achievable for at least 2 weeks post-treatment.
Curiously, the similar levels of downregulation of both SPARC and COL1A1 proteins in the treated tissues on both 7 and 14 days did not correlate with alterations in their transcript levels caused by siSparc treatment. This suggests that reduction of these two proteins, attained at earlier times, was maintained till at least day 14, irrespective of their mRNA levels. We speculate that this phenomenon may be influenced by alterations in specific gene activity as wound healing progresses. It is possible that synthesis of these two proteins reduced dramatically from day 7 to day 14, as suggested by our previous observation that the induction of Col1a1 transcription was highest on day 7 postsurgery but dropped thereafter.28 Low production of COL1A1, and likely SPARC, coupled with potentially low degradation, may then lead to minimal additional accumulation of these two proteins at the later time point so that the levels measured on day 14 were mainly derived from synthesis at earlier times. This phenomenon, although dependent on the biological properties of the specific genes/proteins concerned, is highly beneficial in terms of antifibrotic therapy and does suggest that at least for SPARC and COL1A1, long-term inhibition at the transcript levels may not be necessary to achieve sustained therapeutic reduction of collagen accumulation in the remodelling tissue.
In summary, we show in this proof-of-principle study that targeted therapy via siRNA is a promising application in improving GFS success along with a reduced surgical morbidity. By targeting SPARC as well as a range of potential ECM targets associated with fibrosis, the data presented here advances oligonucleotide therapeutics as potentially effective antifibrotic therapies for postoperative conjunctival fibrosis. Moreover, we predict that advanced, compact nanocarriers with the capacity to deliver large loads of siRNA in a single dose will be extremely useful for the development of genetic inhibition as targeted therapy in the eye.
We would like to thank Alice Ng and Nyein Chan Lwin from Singapore Eye Research Institute for assistance with animal experiments.
LFS and YFT contributed equally.
Contributors LFS analysed the data and wrote the manuscript. LFS, YFT, LZT and SCWL performed the experiments. SV and TTW conceptualised the study. TTW edited and approved the manuscript.
Funding This work was funded by a Clinician Scientist Award grant (NMRC/CSA-SI/0001/2015) and by the Singapore National Research Foundation under its Translational and Clinical Research (TCR) Programme (NMRC/TCR/002-SERI/2008; NMRC/TCR/008-SERI/2013) to TTW, both administered by the Singapore Ministry of Health’s National Medical Research Council. Animal studies were funded by a SingHealth Foundation Research Grant (SHF/FG583P/2014) to LFS and partially funded by the SERI core grant (NMRC/CG/015/2013).
Competing interests None declared.
Patient consent Not required.
Ethics approval Institutional Animal Care and Use Committee (IACUC).
Provenance and peer review Not commissioned; externally peer reviewed.
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