RESUMEN
A lack of ectodysplasin-A (Eda) signaling leads to dry eye symptoms, which have so far only been associated with altered Meibomian glands. Here, we used loss-of-function (Eda-/-) mutant mice to unravel the impact of Eda signaling on lacrimal gland formation, maturation and subsequent physiological function. Our study demonstrates that Eda activity is dispensable during lacrimal gland embryonic development. However, using a transcriptomic approach, we show that the Eda pathway is necessary for proper cell terminal differentiation in lacrimal gland epithelium and correlated with modified expression of secreted factors commonly found in the tear film. Finally, we discovered that lacrimal glands present a bilateral reduction of Eda signaling activity in response to unilateral corneal injury. This observation hints towards a role for the Eda pathway in controlling the switch from basal to reflex tears, to support corneal wound healing. Collectively, our data suggest a crucial implication of Eda signaling in the cornea-lacrimal gland feedback loop, both in physiological and pathophysiological conditions. Our findings demonstrate that Eda downstream targets could help alleviate dry eye symptoms.
Asunto(s)
Córnea/fisiología , Ectodisplasinas/fisiología , Retroalimentación Fisiológica/fisiología , Aparato Lagrimal/fisiología , Animales , Células Cultivadas , Córnea/embriología , Síndromes de Ojo Seco/genética , Síndromes de Ojo Seco/terapia , Ectodisplasinas/genética , Embrión de Mamíferos , Aparato Lagrimal/embriología , Glándulas Tarsales/embriología , Glándulas Tarsales/fisiología , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Transducción de Señal/genética , Lágrimas/fisiologíaRESUMEN
The tear film is produced by two ocular glands, the lacrimal glands, which produce the aqueous component of this film, and the meibomian glands, which secrete the lipidic component that is key to reduce evaporation of the watery film at the surface of the eye. Embryonic development of these exocrine glands has been mostly studied in mice, which also develop Harderian glands, a third type of ocular gland whose role is still not well understood. This review provides an update on the signalling pathways, transcription factors andextracellular matrix components that have been shown to play a role in ocular gland development.
Asunto(s)
Ojo/embriología , Glándula de Harder/embriología , Aparato Lagrimal/embriología , Glándulas Tarsales/embriología , Animales , Ojo/metabolismo , Regulación del Desarrollo de la Expresión Génica , Glándula de Harder/metabolismo , Humanos , Aparato Lagrimal/metabolismo , Glándulas Tarsales/metabolismo , Organogénesis/genética , Transducción de Señal/genética , Lágrimas/metabolismoRESUMEN
The epidermal growth factor receptor (EGFR) signaling has a pivotal role in the regulation of morphogenesis during development and maintenance of homeostasis in adult eyelid and its adnexa. Studies have demonstrated that during eyelid morphogenesis the EGFR signaling pathway is responsible for keratinocyte and mesenchymal cell proliferation and migration at the eyelid tip. For meibomian gland morphogenesis, EGFR signaling activation stimulates meibomian gland epithelial cell proliferation. EGFR signaling pathway functions through multiple downstream signals such as ERK, Rho/ROCK and integrin and is regulated by a variety of upstream signals including Adam17, GPR48 and FGFR signaling. Herein we review the literature that describe the role of EGFR and its related signaling pathways in eyelid and meibomian gland morphogenesis.
Asunto(s)
Receptores ErbB/fisiología , Párpados/embriología , Glándulas Tarsales/embriología , Movimiento Celular/fisiología , Proliferación Celular/fisiología , Células Epiteliales/fisiología , Párpados/fisiología , Humanos , Glándulas Tarsales/fisiología , Transducción de Señal/fisiologíaRESUMEN
Transforming growth factor alpha (TGFα) belongs to the epidermal growth factor (EGF) family and is known to play an important role during eyelid morphogenesis. In this study, we showed that ectopic expression of TGFα in the stroma of Kera-rtTA/tet-O-TGFα bitransgenic mice results in precocious eye opening, abnormal morphogenesis of the meibomian gland, tendon and tarsal plate malformation and epithelium hyperplasia. TGFα did not change proliferation and differentiation of meibocytes, but promoted proliferation and inhibited differentiation of the tarsal plate tenocytes. These results suggest that proper formation of the tendon and tarsal plate in the mouse eyelid is required for normal morphogenesis of the meibomian gland.
Asunto(s)
Párpados/embriología , Regulación del Desarrollo de la Expresión Génica/fisiología , Glándulas Tarsales/anomalías , Morfogénesis/fisiología , Factor de Crecimiento Transformador alfa/metabolismo , Animales , Diferenciación Celular/fisiología , Proliferación Celular/fisiología , Cartilla de ADN/genética , Regulación del Desarrollo de la Expresión Génica/genética , Técnicas Histológicas , Inmunohistoquímica , Glándulas Tarsales/embriología , Ratones , Ratones Transgénicos , Reacción en Cadena de la Polimerasa , Tendones/citología , Tendones/embriología , Factor de Crecimiento Transformador alfa/genéticaRESUMEN
PURPOSE: Mammalian eye development requires temporary fusion of the upper and lower eyelids in embryogenesis. Failure of lid closure in mice leads to an eye open at birth (EOB) phenotype. Many genetic mutant strains develop this phenotype and studies of the mutants lead to a better understanding of the signaling mechanisms of morphogenesis. The present study investigates the roles of lid closure in eye development. METHODS: Seven mutant mouse strains were generated by different gene ablation strategies that inactivated distinct signaling pathways. These mice, including systemic ablation of Map3k1 and Dkk2, ocular surface epithelium (OSE) knockout of c-Jun and Egfr, conditional knockout of Shp2 in stratified epithelium (SE), as well as the Map3k1/Jnk1 and Map3k1/Rhoa compound mutants, all exhibited defective eyelid closure. The embryonic and postnatal eyes in these mice were characterized by histology and immunohistochemistry. RESULTS: Some eye abnormalities, such as smaller lens in the Map3k1-null mice and Harderian gland hypoplasia in the Dkk2-null mice, appeared to be mutant strain-specific, whereas other abnormalities were seen in all mutants examined. The common defects included corneal erosion/ulceration, meibomian gland hypoplasia, truncation of the eyelid tarsal muscles, failure of levator palpebrae superioris (LPS) extension into the upper eyelid and misplacement of the inferior oblique (IO) muscle and inferior rectus (IR) muscle. The muscle defects were traced to the prenatal fetuses. CONCLUSIONS: In addition to providing a protective barrier for the ocular surface, eyelid closure in embryogenesis is required for the development of ocular adnexa, including eyelid and extraocular muscles.
Asunto(s)
ADN/genética , Desarrollo Embrionario/genética , Proteínas del Ojo/genética , Párpados/embriología , Regulación del Desarrollo de la Expresión Génica , Glándulas Tarsales/embriología , Preñez , Animales , Movimiento Celular , Proliferación Celular , Proteínas del Ojo/biosíntesis , Femenino , Immunoblotting , Inmunohistoquímica , Ratones , Ratones Noqueados , Fenotipo , Embarazo , Transducción de SeñalRESUMEN
Murine lacrimal, harderian and meibomian glands develop from the prospective conjunctival and eyelid epithelia and produce secretions that lubricate and protect the ocular surface. Sox9 expression localizes to the presumptive conjunctival epithelium as early as E11.5 and is detected in the lacrimal and harderian glands as they form. Conditional deletion showed that Sox9 is required for the development of the lacrimal and harderian glands and contributes to the formation of the meibomian glands. Sox9 regulates the expression of Sox10 to promote the formation of secretory acinar lobes in the lacrimal gland. Sox9 and FGF signaling were required for the expression of cartilage-associated extracellular matrix components during early stage lacrimal gland development. Fgfr2 deletion in the ocular surface epithelium reduced Sox9 and eliminated Sox10 expression. Sox9 deletion from the ectoderm did not affect Fgf10 expression in the adjacent mesenchyme or Fgfr2 expression in the epithelium, but appeared to reduce FGF signaling. Sox9 heterozygotes showed a haploinsufficient phenotype, in which the exorbital branch of the lacrimal gland was absent in most cases. However, enhancement of epithelial FGF signaling by expression of a constitutively active FGF receptor only partially rescued the lacrimal gland defects in Sox9 heterozygotes, suggesting a crucial role of Sox9, downstream of FGF signaling, in regulating lacrimal gland branching and differentiation.
Asunto(s)
Glándula de Harder/embriología , Aparato Lagrimal/embriología , Glándulas Tarsales/embriología , Morfogénesis/fisiología , Factor de Transcripción SOX9/metabolismo , Transducción de Señal/fisiología , Animales , Factor 10 de Crecimiento de Fibroblastos/metabolismo , Técnicas Histológicas , Inmunohistoquímica , Hibridación Fluorescente in Situ , Captura por Microdisección con Láser , Ratones , Análisis por Micromatrices , Morfogénesis/genética , Factores de Transcripción SOXE/metabolismoRESUMEN
PURPOSE: During mammalian embryonic eyelid closure ADAM17 has been proposed to play a role as a transactivator of epidermal growth factor receptor (EGFR) signaling by shedding membrane bound EGFR ligands. However, ADAM17 also sheds numerous other ligands, thus implicating ADAM17 in additional molecular pathways. The goal of this study was to experimentally establish the role of ADAM17 and determine ADAM17-mediated pathways essential for the embryonic eyelid closure. METHODS: Wild-type (WT) and woe mice, carrying a hypomorphic mutation in Adam17, were evaluated using H&E and scanning electron microscopy. Expressions of ADAM17, EGFR, and the phosphorylated form EGFR-P were evaluated using immunohistochemistry. BrdU and TUNEL assays were used to evaluate cell proliferation and apoptosis, respectively. In vitro scratch assays of primary cultures were used to evaluate cell migration. Clinical and histologic analyses established if the hypermorphic Egfr(Dsk5) allele can rescue the woe embryonic eyelid closure. RESULTS: woe mice exhibited a failure to develop the leading edge of the eyelid and consequently failure of the embryonic eyelid closure. Expression of ADAM17 was identified in the eyelid epithelium in the cells of the leading edge. ADAM17 is essential for epithelial cell migration, but does not play a role in proliferation and apoptosis. EGFR was expressed in both WT and woe eyelid epithelium, but the phosphorylated EGFR-P form was detected only in WT. The Egfr(Dsk5) allele rescued woe eyelid closure defects, but also rescued woe anterior segment defects and the absence of meibomian glands. CONCLUSIONS: We provide in vivo genetic evidence that the role of ADAM17 during embryonic eyelid closure is to transactivate EGFR signaling.
Asunto(s)
Proteínas ADAM/metabolismo , Receptores ErbB/metabolismo , Párpados/embriología , Párpados/metabolismo , Transducción de Señal/fisiología , Proteínas ADAM/genética , Proteína ADAM17 , Animales , Muerte Celular/fisiología , Movimiento Celular/fisiología , Proliferación Celular , Párpados/anomalías , Párpados/citología , Femenino , Regulación del Desarrollo de la Expresión Génica/fisiología , Genotipo , Ligandos , Masculino , Glándulas Tarsales/citología , Glándulas Tarsales/embriología , Glándulas Tarsales/fisiología , Ratones , Ratones Endogámicos C57BL , Ratones Mutantes , Fenotipo , Embarazo , Cultivo Primario de CélulasRESUMEN
PURPOSE: The purpose of this study was to characterize the natural history of meibomian gland morphogenesis in the mouse. METHODS: Embryonic (E) and post natal (P) C57Bl/6 mouse pups were obtained at E18.5, P0, P1, P3, P5, P8, P15, and P60. Eyelids were fixed and processed for en bloc staining with Phalloidin/DAPI to identify gland morphogenesis, or frozen for immunohistochemistry staining with Oil red O (ORO) to identify lipid and antibodies specific against peroxisome proliferator-activated receptor gamma (PPARgamma) to identify meibocyte differentiation. Samples were then evaluated using a Zeiss 510 Meta laser scanning confocal microscope or Nikon epi-fluorescent microscope. Tissues from adult mice (2 month-old) were also collected for western blotting. RESULTS: Meibomian gland morphogenesis was first detected at E18.5 with the formation of an epithelial placode within the fused eyelid margin. Invagination of the epithelium into the eyelid was detected at P0. From P1 to P3 there was continued extension of the epithelium into the eyelid. ORO and PPARgamma staining was first detected at P3, localized to the central core of the epithelial cord thus forming the presumptive ductal lumen. Ductal branching was first detected at P5 associated with acinar differentiation identified by ORO and PPARgamma staining. Adult meibomian glands were observed by P15. Western blotting of meibomian gland proteins identified a 50 kDa and a 72 kDa band that stained with antibodies specific to PPARgamma. CONCLUSIONS: We have demonstrated that meibomian gland development bears distinct similarities to hair development with the formation of an epithelial placode and expression of PPARgamma co-incident with lipid synthesis and meibocyte differentiation.
Asunto(s)
Glándulas Tarsales/embriología , Morfogénesis , Animales , Diferenciación Celular , Núcleo Celular/metabolismo , Lípidos/biosíntesis , Glándulas Tarsales/citología , Glándulas Tarsales/metabolismo , Ratones , Ratones Endogámicos C57BL , Microscopía Confocal , PPAR gamma/metabolismoRESUMEN
The Meibomian glands are large sebaceous glands that are located as separate gland strands in parallel arrangement within the tarsal plates of the eyelids. Their oily product (meibum) is secreted by a holocrine mechanism during which the secretory cells (meibocytes) are completely transformed into the meibum after synthesis and accumulation of lipids. After production in the gland acini, meibum is transported through the ductal system via the connecting duct (ductule) and the central duct towards the orifice at the free lid margin close to the inner lid border. The embryological development of the Meibomian glands takes place during the differentiation of the eyelids in the sealing phase of the eyelids. They are not directly associated with hair follicles but share important similarities in embryology, structure and keratinization potency with the cilia. Similar to the sebaceous glands Meibomian glands are regulated via sex hormones and androgens have a supporting function whereas estrogens act antagonistically. However, in contrast to other sebaceous glands they also have a distinct innervation, apart from sympathetic and sensory primarily by parasympathetic fibers that share the innervation pattern of the lacrimal glands. The anatomy, embryology and histology of the Meibomian glands are explained here, mainly with respect to humans, in an extensive review.