Molecular Vision 2019; 25:129-142
Received 08 September 2018 | Accepted 15 February 2019 | Published 17 February 2019
1Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California Davis, Davis, CA; 2Department of Ophthalmology & Vision Science, School of Medicine, School of Medicine, University of California Davis, Davis, CA; 3Department of Basic Sciences, College of Optometry, University of Houston, Houston, TX; 4The Ocular Surface Institute, College of Optometry, University of Houston, Houston, TX; 5Department of Biomedical Engineering, Cullen College of Engineering, University of Houston, Houston, TX; 6Comparative Ocular Pathology Laboratory of Wisconsin, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI; 7Department of Cell Biology and Human Anatomy, School of Medicine, School of Medicine, University of California Davis, Davis, CA
Correspondence to: Christopher J. Murphy, UC Davis School of Veterinary Medicine Surgical and Radiological Sciences, 1220 Tupper, 1 Shield Avenue, Davis, CA 95616; Phone: (530) 752-0926; FAX: (530) 752-7308; email:email@example.com
Purpose: To identify the effects of a single copy deletion of Yap1 (Yap1+/−) in the mouse eye, the ocular phenotypic consequences of Yap1+/− were determined in detail.
Methods: Complete ophthalmic examinations, as well as corneal esthesiometry, the phenol red thread test, intraocular pressure, and Fourier-domain optical coherence tomography were performed on Yap1+/− and age-matched wild-type (WT) mice between eyelid opening (2 weeks after birth) and adulthood (2 months and 1 year after birth). Following euthanasia, enucleated eyes were characterized histologically.
Results: Microphthalmia with small palpebral fissures, corneal fibrosis, and reduced corneal sensation were common findings in the Yap1+/− mice. Generalized corneal fibrosis precluded clinical examination of the posterior structures. Histologically, thinning and keratinization of the corneal epithelium were observed in the Yap1+/− mice in comparison with the WT mice. Distorted collagen fiber arrangement and hypercellularity of keratocytes were observed in the stroma. Descemet’s membrane was extremely thin and lacked an endothelial layer in the Yap1+/− mice. The iris was adherent to the posterior cornea along most of its surface creating a distorted contour. Most of the Yap1+/− eyes were microphakic with swollen fibers and bladder cells. The retinas of the Yap1+/− mice were normal at 2 weeks and 2 months of age, but the presence of retinal abnormalities, including retinoschisis and detachment, was markedly increased in the Yap1+/− mice at 1 year of age.
Conclusions: The results show that the heterozygous deletion of the Yap1 gene in mice leads to complex ocular abnormalities, including microphthalmia, corneal fibrosis, anterior segment dysgenesis, and cataract.
Yes-associated protein (YAP) is a transcriptional coactivator encoded by the gene YAP1 (Gene ID 22601; OMIM 606608)  which activates gene expression by associating with numerous DNA-binding transcription factors . YAP is a key component of the Hippo signaling pathway which plays essential roles in development, organ growth, homeostasis, and cancer [3-5]. Yap1 is essential for the development of multiple organs by regulating cell proliferation including the eye [3,6,7]. Homozygous deletion of the Yap1 gene is known to be lethal to embryos around E8.5 to E9.5 with no evidence of attachment of the allantois to the chorion and failure of ventral closure and turning . However, mice that have single gene deletion of Yap (Yap1+/−) are viable , and a heterozygous mutation in YAP1 has been reported to cause optic fissure closure defects associated with microphthalmia, cataract, and iris coloboma in humans .
Expression of YAP is intimately involved in eye development and corneal wound healing. Whole-mount in situ hybridization in mouse embryos has shown that Yap1 is strongly expressed in the eye . YAP expression has been documented within an array of ocular tissues, including the corneal epithelial and endothelial cells, lens epithelial cells, ciliary body, iris, inner nuclear layer of the retina, and the RPE, in the adult mouse eye . In addition, YAP and TAZ are reported to be key molecules that participate in major signaling pathways relevant to corneal wound healing: mechanotransduction , wingless/integrated (Wnt) , and transforming growth factor beta (TGF-β) [12,13]. They have also been shown to act as mechanotransducers relaying the biophysical attributes of the extracellular matrix into the cells, a process that ultimately influences cell functions [13-16]. Therefore, it is likely that manipulation of the Yap1 gene would affect corneal wound healing.
Mice with heterozygous deletion of the Yap1 gene are viable, but the detailed phenotypic consequences to ocular structures have not been reported. To address the feasibility of using Yap1+/− mice as a corneal wound healing model, the present study was undertaken to determine how a single copy deletion of Yap1 affects ocular phenotypes in mice with an emphasis on examining consequences on the cornea.
Five Yap1 heterozygous (Yap1+/−) male C57BL/6J mice from the Knock Out Mouse Program (KOMP) within the Mouse Biology Program (MBP) at University of California, Davis and 20 female wild-type (WT) C57BL/6J mice from The Jackson Laboratory (Sacramento, CA) were used to generate Yap1+/− mice. Due to the poor fertility of female Yap1+/− mice, male Yap1+/− mice were used to mate with WT females. A total of 318 pups were generated from breeding of these initial 25 mice. All procedures were performed in compliance with the Association for Research in Vision and Ophthalmology (ARVO) Statement for the Use of Animals in Ophthalmic and Vision Research. The study design was approved by the Institutional Animal Care and Use Committee of the University of California, Davis.
Yap1+/− male mice were obtained from the KOMP within the MBP. Mice were cryorecovered via in vitro fertilization using C57BL/6N oocyte donors and Yap1 heterozygous sperm preserved by the KOMP. Fertilized two-cell stage embryos were then transferred surgically to two pseudopregnant CD1 recipients. Pseudopregnancy was induced by mating with sterile vasectomized male mice on day 0, and the manipulated embryos were transferred into these recipients a half day later. Derived pups were genotyped via short-range mutant PCR specific to Yap1 mice with the following primers; CSD-Yap1-SR1: 5′-CAG GCA AGT TTG AGG CTA GTT TCT GG-3′, and Common-loxP-F: 5′-GAG ATG GCA ACG CAA TTA AT-3′. Male Yap1+/− mice C57BL/6J were used to breed to WT C57BL/6J females to generate Yap1+/−. All Yap1+/− mice were tested for the retinal degeneration (Rd8) mutation, and positive Rd8 mutant animals were excluded from breeding to generate Yap1+/− without the Rd8 mutation. This was critical as the Rd8 background has several ocular background findings that may have confounded the study [17,18].
Pups were genotyped with PCR as follows. DNA was extracted from toe clip samples at 7 days after birth or tail clip samples approximately 3 weeks after birth using a DNA extraction kit (DNeasy® Blood & Tissue Kit; QIAGEN Sciences, MD) following the manufacturer’s protocol. The extracted DNA was then confirmed for mutant allele copy number using PCR with the following oligonucleotides: YAP5′: CSD-lacF: 5′-GCT ACC ATT ACC AGT TGG TCT GGT GTC-3′ and YAP3′: CSD-YAP1-R: 5′-TCA AGG CCA TCA TAG ATC CTG GAC G-3′, following thermal cycling: 94 °C for 5 min; 10 cycles of 94 °C for 15 s, 65 °C for 30 s (decrease 1 °C for each cycle), 72 °C for 40 s; 30 cycles of 94 °C for 15 s, 55 °C for 30 s, 72 °C for 40 s; 72 °C for 5 min and hold at 4 °C. The PCR fragments were separated on the E-Gel® 2% Agarose with SYBR SafeTM (Invitrogen, Carlsbad, CA) at 48 V for 45 min using dry-gel system (iBaseTM; Invitrogen) and read with the ChemiDoc-It®2 810 Imager (Ultra-Violet Products Ltd., Cambridge, UK).
Ophthalmic examination and advanced ocular imaging were performed using 26 Yap1+/− and 16 WT mice within three different age groups (Appendix 1B): 2 weeks old (weaning period, eye opening time point; n=6, three Yap1+/− and three WT mice), 2 months old (adult; n=15, eight Yap1+/− and seven WT mice), and 1 year old (aged adult; n=21, fifteen Yap1+/− and six WT mice). For the ophthalmic examination and subsequent measurements, the mice were gently restrained without any pressure to their neck and head. Cochet-Bonnet esthesiometry (Esthesiometer 12/100 mm; LUNEAU Ophthalmologi, Prunay-le-Gillon, France) to determine corneal sensation, a phenol red thread test (PRTT; Zone-Quick, Showa Yakuhin Kako Co., LTD, Tokyo, Japan) to assess aqueous tear production, and rebound tonometry (TonoLab; Icare, Helsinki, Finland) to measure intraocular pressure (IOP) were performed. All mice then received a thorough ophthalmic examination of the anterior and posterior segment using a hand-held slit-lamp (Kowa SL15; Kowa Optimed, Torrance, CA) and indirect ophthalmoscopy (Keeler VANTAGE Plus; Keeler Inc., Broomall, PA) with a 90 D indirect lens (Volk Optical, Inc., Mentor, OH). Following this examination, the mice were sedated with an intraperitoneal (IP) injection of midazolam/hydromorphone (0.7 mg/kg/0.1 mg/kg) for advanced ocular imaging. The palpebral fissure length was measured with digital calipers accurate to 0.1 mm (Fred V. Fowler Co., Inc., Newton, MA). The eyes were photographed with a digital color camera (Canon EOS5D; flash 1/64. ios 200, F16) and slit-lamp biomicroscopy with digital capture (Hagg-Streit BQ 900 Slit Lamp; Hagg-streit, Koeniz, Switzerland). Corneas were imaged with an RTVue-100 Fourier-Domain Optic Coherence Tomography (FD-OCT) system (software version 6.1; Optovue Inc., Fremont, CA; 26,000 A scan/sec, 5 μm axial resolution, 840 nm superluminescent diode) with a CAM-S [S/N 30,107] lens.
Mice were euthanized with pentobarbital (200 mg/kg, IP), and body length was measured with a digital caliper (Fred V. Fowler Co., Inc.). After enucleation of both eyes, one eye of each mouse was fixed using the freeze substitution protocol as described by Sun et al. , and the opposite eye was dedicated for transmission electron microscopy as described below. Briefly, the enucleated mouse eyes were rapidly frozen by immersion in liquid propane at −80 °C for 1 min and then rapidly transferred to 97% methanol and 3% acetic acid at −80 °C. The samples were placed at −80 °C for 48 h and then gradually warmed every 4 h of incubation at −40 °C, −20 °C, and then 20 °C for 48 h. The fixed eyes were then processed using standard protocols and embedded in paraffin wax. Five-micrometer-thick parasagittal sections were obtained from paraffin blocks and stained with hematoxylin and eosin (H&E). Immunofluorochemistry was performed on the 5-μm-thick paraffin-embedded parasagittal sections. Paraffin was dissolved in xylene for 10 min twice, and the samples were rehydrated using a serial dilution of ethanol. After the slides were blocked in 0.03% H2O2 in methanol for 30 min, antigen retrieval was performed by immersing the sample in sodium citric buffer (pH 6.0) with 0.02% Tween-20 in a steamer 56 °C for 30 min, and then cooled to room temperature. Rabbit monoclonal anti-YAP antibody (Cell Signaling Technology, Danvers, MA) at 1:200 dilution in blocking buffer was incubated with the samples for 2 h in 37 °C. The samples were incubated with an appropriate secondary antibody (1:200 dilution, Thermo Scientific Pierce, Rockford, IL) at room temperature for 45 min in the dark. Nuclei were counterstained with 4’-6-diamidino-2-phenylindole (DAPI; Life Technologies, Carlsbad, CA). The stained sections were imaged using an Axiovert 200M epifluorescent microscope (Carl Zeiss Ag, Oberkochen, Germany) with a 20X objective. All images were taken with equal exposure times.
The opposite eye of each mouse was fixed in 2.5% glutaraldehyde and 2% paraformaldehyde in 0.1 M sodium cacodylate buffer, and electron microscopy of the cornea was performed using standard protocols. Briefly, the fixed eyes were rinsed in 0.1 M sodium cacodylate buffer for 15 min twice and then placed in 2% osmium tetroxide for 1 h. The samples were then rinsed in water for 15 min twice. Then, the eyes were dehydrated in 50% ethyl alcohol (EtOH), 75% EtOH, and 95% EtOH for 30 min each and 100% EtOH for 20 min twice. The eyes were then placed in propylene oxide for 15 min twice. Next, the eyes were infiltrated in a Poly/Bed 812 mixture for 4 h and polymerized in a Poly/Bed 812 mixture at 65 °C for at least 24 h. Ultrathin sections were mounted on naked copper grids and stained with 3% uranyl acetate and 0.03% lead citrate before examination with a transmission electron microscope (TEM; Philips CM120 Biotwin Lens, F.E.I. Company, Hillsboro, OR; with Gatan MegaScan, model 794/20, digital camera (2 K × 2 K), Pleasanton, CA; Gatan BioScan, model 792, Pleasanton, CA).
Statistical analysis was performed with a commercially available statistical software program (GraphPad Prism 7.03, GraphPad Software Inc., San Diego, CA). Unpaired Student t tests with Welch’s correction were performed to compare the corneal thickness measurements between the groups. An odds ratio (OR) was calculated to evaluate the incidence rate of female Yap1+/− pups with a Fisher’s exact test. A p value of less than 0.05 was considered statistically significant. Results were expressed as mean ± standard deviation (SD).
Genotyping with PCR was performed on 318 pups of which 285 were WT mice and 33 were Yap1+/− mice. Given that the expected ratio should be 50% WT and 50% Yap1+/− mice, the number of Yap1+/− mice identified was statistically significantly less than the WT mice (Observed %=10.38, 95% confidence interval [CI]: 7.458 to 14.22; p<0.001). In addition, we observed a statistically significantly lower number of female versus male Yap1+/− progeny at eight and 25 mice, respectively (OR=0.387, 95% CI: 0.1794 to 0.902; p=0.025). Generally, the body length of the Yap1+/− mice (26.53±1.39 mm) was statistically significantly shorter than that of the age-matched WT mice (47.68±5.83 mm) at the weaning period (p=0.02), but adult mice were comparable (Table 1). Around 80% of the Yap1+/− mice had abnormal dome-shaped heads (Figure 1A), and some Yap1+/− mice were euthanized because of abnormal seizure-like activity (n=4) or corneal perforation (n=3).
Similar ocular phenotypes were observed in Yap1+/− mice at the ages examined. Microphthalmia with a small palpebral fissure was observed in 67% of the Yap1+/− mice (Figure 1A) with 23% of the eyes of the Yap1+/− mice had no ocular structures clinically detectable with slit-lamp evaluation (Table 2). Generalized corneal fibrosis was present in 85% of the Yap1+/− eyes as assessed with slit-lamp biomicroscopy (Table 2) which often precluded clinical examination of the intraocular structures (Figure 1B). Three Yap1+/− mice were euthanized due to corneal perforation occurring between 2 and 6 months of age, and one eye of a Yap1+/− mouse at 2 months of age developed a perforated cornea with granulation tissue (Figure 1B). Using FD-OCT, a thin cornea with the iris adhered to the posterior aspect and aphakia were commonly observed in the Yap1+/− mice (Figure 2). The central corneal thickness (CCT) of the Yap1+/− mice was significantly thinner at all ages as measured with FD-OCT (p<0.05; Table 1). Only six eyes (two eyes in two 2-month-old mice and four eyes in three 1-year-old mice) of five Yap1+/− mice had corneas with adequate transparency allowing documentation of hypermature cataract and posterior synechiae (Figure 1B and Figure 2). The five Yap1+/− mice with clear corneas were related along paternal lines (Appendix 1C). The anterior segment and fundus of the WT mice were normal on clinical examination and FD-OCT.
The palpebral fissures in the Yap1+/− mice were significantly shorter than those in the WT mice at all ages (p<0.01; Table 1). Corneal touch threshold, as measured with Cochet-Bonnet estheiometry, was significantly lower in the Yap1+/− versus WT mice (p<0.001), but tear production as measured with the PRTT (p>0.05), and intraocular pressure (p>0.05) as measured with rebound tonometry did not differ statistically significantly between the Yap1+/− and the WT mice for the three age groups tested (Table 1). Moreover, the IOP of the Yap1+/− eyes which had clear corneas and normal anterior chamber depths showed no statistically significant differences compared with the Yap1+/− eyes with microphthalmia and corneal fibrosis at 2 months (13.5±2.1 mmHg in two clear corneal eyes versus 13.5±3.9 mmHg in the abnormal eyes; p>0.999) and 1 year of age (10.0±0.0 mmHg in three clear corneal eyes versus 11.6±3.2 mmHg in the abnormal eyes; p=0.865).
YAP expression was detected in the corneal epithelium and endothelium and non-pigmented epithelium of the ciliary body in all groups of the Yap1+/− and WT mice and primarily localized to the cytoplasm in both groups. The expression of YAP was reduced in the Yap1+/− mice compared with WT mice (Figure 3). Interestingly, Yap1+/− mice with clear corneas had greater expression of YAP versus those with corneal fibrosis but had less expression in comparison with the WT mice (Appendix 2).
Histologically, partial or complete collapse of the anterior chamber was observed with broad anterior synechiae in 87% of the Yap1+/− eyes (Figure 4B and Appendix 3). Iris hypoplasia with abnormal iridocorneal angle morphology was observed in 89% of the Yap1+/− eyes (Table 2). The number of corneal epithelial cell layers in the Yap1+/− mice was decreased in comparison with the WT mice (Figure 5 and Appendix 3) with loss of polygonal wing cells and superficial cells. In the corneal stroma, distorted stromal fibers, hypercellularity of corneal stromal, and rare focal edema with stromal neovascularization were observed in the Yap1+/− mice (Figure 5B). Descemet’s membrane was absent in 86% of the Yap1+/− mice eyes (Table 2).
Corneal abnormalities observed with TEM were consistent with those observed with bright-field microscopy in all ages of Yap1+/− mice with multiple ultrastructural lesions identified. In the WT mice, the corneal epithelium comprised seven to nine layers of keratinocytes with clearly identifiable differentiation among the basal, wing cell, and superficial squamous cell layers (Figure 6A). In contrast, the Yap1+/− mice demonstrated marked thinning of the superficial squamous cell layer and a lack of microvilli on the apical surface of the most superficial keratinocytes (Figure 6B). The corneal stroma on the Yap1+/− mice showed increased cellularity due to the presence of fusiform cells between the stromal lamellae with an abundant vacuolar cytoplasm and oval nuclei, consistent with reactive keratocytes (Figure 6B); spindle-shaped keratocytes were localized between the stromal lamellae in the WT mice. The Yap1+/− mice also had a thin Descemet’s membrane compared to the age-matched WT mice and lacked a recognizable endothelial cell layer, which was replaced by a layer of melanin-laden cuboidal cells (Figure 6).
Hypermature cataract and posterior synechiae were documented in the five Yap1+/− mice that had transparent corneas with a slit-lamp examination and imaging (Figure 1B and Figure 3); the age-matched WT mice showed no lens abnormalities. Clinical evaluation of the lens could not be performed in the remaining 28 Yap1+/− mice due to microphthalmia, corneal fibrosis, and anterior synechiae.
In cases where the lens could be identified clinically, histopathological features of included microphakia with hypermature cataract (Figure 4D). The cataractous changes were represented by marked degeneration and liquefaction of the lens fibers, formation of morgagnian globules, bladder cells, and posterior migration of the lens epithelium in 60% of total Yap1+/− eyes or 96% of the Yap1+/− eyes where a lens was present (Table 2). In 40% of the Yap1+/− eyes, a lens could not be found on histologic evaluation, and the eyes were considered aphakic (Table 2). Additional lens findings included abnormal lens capsules (Figure 4D) and frank posterior lens capsule rupture with extruded degenerate lens fibers (Table 2).
The fundus could not be clinically evaluated in any Yap1+/− mice due to opacification of the cornea or cataracts; the fundus of all WT mice was assessed as normal. Histologically, retinal morphology was typically normal in WT and Yap1+/− mice at 2 weeks and 2 months of age (Appendix 4). Persistent hyaloid artery (HA) and tunica vasculosa lentis (TVL) were commonly observed at 2 weeks after birth in the WT and Yap1+/− mice as normal developmental findings. Seven eyes of 2-month-old Yap1+/− mice had normal retinal morphology while two eyes had retinoschisis (n=2) and focally extensive areas of retinal detachment (n=1; Table 2). In the Yap1+/− mice, the incidence of retinal abnormalities, including retinal detachment and retinoschisis, was greater in the 1-year-old age group than in the 2-week-old and 2-month-old age groups in the Yap1+/− mice (Table 2). In the 1-year-old Yap1+/− mice, retinal detachment with loss of the RPE and subretinal accumulation of macrophages were common findings (Table 2 and Figure 5D); retinal thinning with loss of outer nuclear, photoreceptor, and RPE layers accompanied retinal detachment (Figure 5D). Retinoschisis was observed in 36% of the 1-year-old Yap1+/− mice, and it was characterized by focally extensive vacuolization of the inner nuclear layer and/or separation of the internal limiting membrane from the nerve fiber layer (Figure 5D). Rosette formation in the photoreceptor layer was also identified in two 1-year-old Yap1+/− mice.
The present study investigated the ocular phenotypic consequences of a single copy deletion of the Yap1 gene. In addition to profound anterior segment abnormalities, the data suggest that haploinsufficiency of Yap1 promotes embryonic death and in survivors, developmental consequences, as indicated by the shorter body length in the Yap1+/− versus WT mice, ocular and adnexal abnormalities, and the development of a dome-shaped head in some animals. Yap1 is required to promote early chondrocyte proliferation and its subsequent maintenance . These critical functions likely contributed to the smaller body size observed in the Yap1+/− mice and may have contributed to the development of a dome-shaped head. In the present study, male Yap1+/− mice were used to mate with the WT females to generate additional Yap1+/− mice because female Yap1+/− mice are unable to be fertilized due to a lack of ovarian follicular growth [21,22]. Only 10% of the pups generated in this study were genotyped as Yap1+/− which is consistent with previous studies reporting between 12.5% and 16.7% . Given the important myriad roles that YAP and Hippo signaling [8,23] play throughout development, it is unsurprising that knockout of even one copy of Yap1 often results in embryonic death. Moreover, the phenotypic consequences of single gene deletion of Yap1 was widely variable. A range of ocular phenotypic consequences was observed in this study. Although all animals had ocular abnormalities, the extent of the ocular involvement varied. This is best exemplified by the corneal findings that ranged from normal to markedly abnormal. This variability is likely the consequence of the interplay between the “noise” in gene expression and the complex downstream effects on regulatory networks [24,25]. Variability in phenotypic consequences for the deletion of Yap65 has been reported in mice  as well as functional mutation of YAP1 in human clinical studies . Interestingly, in this study, the Yap1+/− mice possessing a clear cornea (but cataract) were all related along paternal lines, and greater expression of YAP was observed in these animals in the cornea and ciliary body than in the Yap1+/− mice with more severe corneal involvement.
The eyes of the Yap1+/− mice were often microphthalmic with a narrowed palpebral fissure consistent with previous studies in the yap1 knockdown of Xenopus tadpoles  and the conditional knockout of Yap in mouse embryos . YAP is a key regulator of organ size and tissue homeostasis. Hippo signaling controls organ size by phosphorylating and inhibiting the transcriptional coactivator YAP . In the mouse liver, Yap1 induction increases the organ size and causes aberrant tissue expansion . Our finding of microphthalmia in the Yap1+/− eyes is consistent with these studies in other organs and suggests that YAP expression is necessary for normal eye development.
Anterior segment dysgenesis (ASD) consisting of corneal fibrosis, lack of proper formation of the anterior chamber, iris hypoplasia, and cataract were commonly observed in the Yap1+/− mice at all examined ages. In particular, the Yap1+/− mice exhibited marked cataractous changes that may be due to a close regulatory relationship between Hippo-YAP signaling or the Notch/Wnt signaling pathway. Yap is shown to activate target genes in Wnt signaling . Hippo-YAP signaling is critical to lens development by modulating Notch signaling and subsequent lens epithelial cell migration [29,30].
Numerous ocular developmental studies in mice support that improper lens development can result in abnormal anterior segment formation [31,32]. Signals from the lens epithelium are required for proper differentiation of the cells that form the anterior structures of the eye, including the corneal endothelium [33,34] and the ciliary epithelium . Neural crest-derived mesenchymal cells also contribute to the proper development of the iris, ciliary process, corneal stroma, and endothelium [31,36]. In aggregate, it is clear the lens is important for the mesenchymal-to-epithelial transformation that accompanies the formation of the corneal endothelium. Thus, the markedly thin or absent Descemet’s membrane without an endothelium observed in most of the Yap1+/− mice may be a result of abnormal lens development.
YAP and TAZ are known to be present in the normal human trabecular meshwork (HTM) , and the expression of YAP is dramatically influenced by substratum compliance in primary HTM cells . Moreover, a stiffer HTM associated with primary open angle glaucoma results in nuclear localization of YAP and TAZ that subsequently increases gene expression . In this study, the Yap1+/− mice had an improperly formed iridocorneal angle and abnormal trabecular meshwork structures but also a poorly developed ciliary body and an absent anterior chamber suggesting that aqueous humor outflow and production are likely abnormal. Thus, these marked anterior segment changes prevented further study of the role that YAP may play in the aqueous outflow in Yap1+/− mice. When considering that the severity of clinically detected ASD does not correlate with IOP elevation in other mouse models as well as human patients , it is not surprising that the Yap1+/− mice demonstrated no alterations in IOP at any examined age in the present study.
YAP is reported to be essential for normal retinal development  and is specifically expressed in Müller cells and the RPE . In the present study, the retinal architecture in the Yap1+/− mice was similar to that of their normal WT littermates at 2 weeks and 2 months of age. However, numerous retinal abnormalities were observed in the aged Yap1+/− mice, including loss of the RPE and outer nuclear and photoreceptor layers, retinal detachment, or retinoschisis. YAP signaling has various functions in the retina that are age-dependent . YAP is a key regulator of RPE genesis , as well as cell proliferation and dedifferentiation in RPE cells . Decreasing YAP expression has been reported to reduce proliferation and increase differentiation in the postnatal mouse retina . Taken together, these studies demonstrate that Yap1 has multiple roles in retinal development and health that are consistent with the age-dependent retinal changes identified in the present study.
Retinoschisis is caused by a mutation in the retinoschisin (RS1) gene, known to express a cell adhesion protein that binds tightly to the surface of photoreceptors and bipolar cells to maintain the cellular organization in the retina . Experimental mouse models such as the RS1 knockout  and RS1 knock-in  have been developed to study the clinical effects of retinoschisis. However, to the authors’ knowledge a relation between retinoschisis and Yap1 has not been reported. The present study is the first to report that retinoschisis occurs as a consequence of a single copy deletion in Yap1. Further studies are needed to explore the potential link(s) between the RS1 gene and the YAP/TAZ signaling pathway.
This study focused on the phenotypic characterization of Yap1+/− eyes because our motivation was to study the role of YAP in corneal wound healing. YAP is important in corneal epithelial cell proliferation and the formation of tight junctions . Moreover, because YAP is related to stem cell expression , alteration of YAP could cause disruption of cornmeal epithelial limbal stem cell function. Unfortunately, the marked corneal changes in the Yap1+/− mice prevented study of corneal epithelial and stromal wound healing. We note that three mice were euthanized due to the corneal perforation between 2 and 6 months of age. In contrast, no corneal abnormalities were found in any WT mice at any age. The loss of corneal integrity could be related to disruption of YAP signaling impairing the maintenance of corneal homeostasis and negatively impacting corneal wound healing. Therefore, a conditional knockout mouse would be necessary to study the role of YAP in corneal epithelial and stromal wound healing, and a recent study using such mice demonstrated that YAP signaling is crucial for corneal epithelial regeneration and wound healing .
In conclusion, the Yap1+/− mice demonstrated microphthalmia, hypoplastic, dysplastic, and fibrotic corneas with anterior segment dysgenesis, cataract, and retinal changes. Due to the complete loss of corneal transparency accompanied by corneal fibrosis, corneal wound healing could not be investigated using the Yap1+/− mouse suggesting that conditional knockouts are necessary. In aggregate, these results support that YAP signaling is critical for the proper formation and maintenance of the normal ocular structures in the eye.
The authors thank Paul Russell for his support and Monica Motta, Ariana Marangakis, Carina Pasqualino, Madison Mukai and Daniel Madrigal for excellent technical assistance; Bradley Shibata for assistance in slide preparation and TEM imaging. This study was funded by grants from the National Institute of Health R01EY016134, R01EY019970, K08EY027463 and P30EY12576.