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1.
PLoS One ; 9(11): e112142, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25392995

RESUMO

Cell death in neurodegenerative diseases is often thought to be governed by apoptosis; however, an increasing body of evidence suggests the involvement of alternative cell death mechanisms in neuronal degeneration. We studied retinal neurodegeneration using 10 different animal models, covering all major groups of hereditary human blindness (rd1, rd2, rd10, Cngb1 KO, Rho KO, S334ter, P23H, Cnga3 KO, cpfl1, Rpe65 KO), by investigating metabolic processes relevant for different forms of cell death. We show that apoptosis plays only a minor role in the inherited forms of retinal neurodegeneration studied, where instead, a non-apoptotic degenerative mechanism common to all mutants is of major importance. Hallmark features of this pathway are activation of histone deacetylase, poly-ADP-ribose-polymerase, and calpain, as well as accumulation of cyclic guanosine monophosphate and poly-ADP-ribose. Our work thus demonstrates the prevalence of alternative cell death mechanisms in inherited retinal degeneration and provides a rational basis for the design of mutation-independent treatments.


Assuntos
Morte Celular/fisiologia , Degeneração Retiniana/fisiopatologia , Animais , Animais Geneticamente Modificados , Calpaína/fisiologia , Morte Celular/genética , GMP Cíclico/fisiologia , Modelos Animais de Doenças , Histona Desacetilases/fisiologia , Transdução de Sinal Luminoso/genética , Camundongos , Mutação , Poli Adenosina Difosfato Ribose/fisiologia , Poli(ADP-Ribose) Polimerases/fisiologia , Ratos , Degeneração Retiniana/genética
2.
Mol Vis ; 19: 2312-20, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24265546

RESUMO

PURPOSE: To analyze in vivo the function of chicken acidic leucine-rich epidermal growth factor-like domain containing brain protein/Neuroglycan C (gene symbol: Cspg5) during retinal degeneration in the Rpe65⁻/⁻ mouse model of Leber congenital amaurosis. METHODS: We resorted to mice with targeted deletions in the Cspg5 and retinal pigment epithelium protein of 65 kDa (Rpe65) genes (Cspg5⁻/⁻/Rpe65⁻/⁻). Cone degeneration was assessed with cone-specific peanut agglutinin staining. Transcriptional expression of rhodopsin (Rho), S-opsin (Opn1sw), M-opsin (Opn1mw), rod transducin α subunit (Gnat1), and cone transducin α subunit (Gnat2) genes was assessed with quantitative PCR from 2 weeks to 12 months. The retinal pigment epithelium (RPE) was analyzed at P14 with immunodetection of the retinol-binding protein membrane receptor Stra6. RESULTS: No differences in the progression of retinal degeneration were observed between the Rpe65⁻/⁻ and Cspg5⁻/⁻/Rpe65⁻/⁻ mice. No retinal phenotype was detected in the late postnatal and adult Cspg5⁻/⁻ mice, when compared to the wild-type mice. CONCLUSIONS: Despite the previously reported upregulation of Cspg5 during retinal degeneration in Rpe65⁻/⁻ mice, no protective effect or any involvement of Cspg5 in disease progression was identified.


Assuntos
Proteínas de Membrana/metabolismo , Proteoglicanas/metabolismo , Degeneração Retiniana/genética , cis-trans-Isomerases/genética , Animais , Regulação da Expressão Gênica , Proteínas de Membrana/deficiência , Camundongos , Especificidade de Órgãos/genética , Proteoglicanas/deficiência , Células Fotorreceptoras Retinianas Cones/metabolismo , Células Fotorreceptoras Retinianas Cones/patologia , Degeneração Retiniana/patologia , Células Fotorreceptoras Retinianas Bastonetes/metabolismo , Células Fotorreceptoras Retinianas Bastonetes/patologia , Fatores de Tempo , cis-trans-Isomerases/deficiência , cis-trans-Isomerases/metabolismo
3.
PLoS One ; 8(2): e55372, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23383327

RESUMO

α-Crystallins, initially described as the major structural proteins of the lens, belong to the small heat shock protein family. Apart from their function as chaperones, α-crystallins are involved in the regulation of intracellular apoptotic signals. αA- and αB-crystallins have been shown to interfere with the mitochondrial apoptotic pathway triggering Bax pro-apoptotic activity and downstream activation of effector caspases. Differential regulation of α-crystallins has been observed in several eye diseases such as age-related macular degeneration and stress-induced and inherited retinal degenerations. Although the function of α-crystallins in healthy and diseased retina remains poorly understood, their altered expression in pathological conditions argue in favor of a role in cellular defensive response. In the Rpe65⁻/⁻ mouse model of Leber's congenital amaurosis, we previously observed decreased expression of αA- and αB-crystallins during disease progression, which was correlated with Bax pro-death activity and photoreceptor apoptosis. In the present study, we demonstrated that α-crystallins interacted with pro-apoptotic Bax and displayed cytoprotective action against Bax-triggered apoptosis, as assessed by TUNEL and caspase assays. We further observed in staurosporine-treated photoreceptor-like 661W cells stably overexpressing αA- or αB-crystallin that Bax-dependent apoptosis and caspase activation were inhibited. Finally, we reported that the C-terminal extension domain of αA-crystallin was sufficient to provide protection against Bax-triggered apoptosis. Altogether, these data suggest that α-crystallins interfere with Bax-induced apoptosis in several cell types, including the cone-derived 661W cells. They further suggest that αA-crystallin-derived peptides might be sufficient to promote cytoprotective action in response to apoptotic cell death.


Assuntos
Apoptose/fisiologia , Sobrevivência Celular/fisiologia , Citoproteção/fisiologia , Cadeia A de alfa-Cristalina/metabolismo , Proteína X Associada a bcl-2/metabolismo , Animais , Apoptose/genética , Western Blotting , Caspases/metabolismo , Sobrevivência Celular/genética , Clonagem Molecular , Citoproteção/genética , Primers do DNA/genética , Vetores Genéticos , Células HEK293 , Humanos , Imunoprecipitação , Marcação In Situ das Extremidades Cortadas , Lentivirus , Camundongos , Microscopia de Fluorescência , Cadeia A de alfa-Cristalina/genética
4.
Exp Eye Res ; 96(1): 70-81, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22227450

RESUMO

RPE65-related Leber's congenital amaurosis (LCA) is a rod-cone dystrophy whose clinical outcome is mainly attributed to the loss of rod photoreceptors followed by cone degeneration. Pathogenesis in Rpe65(-/-) mice is characterized by a slow and progressive degeneration of rods dependent on the constitutive activation of unliganded opsin. We previously reported that this opsin-mediated apoptosis of rods was dependent on Bcl-2-apoptotic pathway and Bax-induced pro-death activity. In this study, we report early initial apoptosis in the newly differentiated retina of Rpe65(-/-) mice. Apoptotic photoreceptors were identified as rods and resulted from pathological phototransduction signaling. This wave of early apoptosis triggered Bcl-2-related pathway and Bax apoptotic activity, while activation of the caspases was not induced. Following cellular stress, multiple signaling pathways are initiated which either commit cells to death or trigger pro-survival responses including autophagy. We report that Bcl-2-related early rod apoptosis was associated with the upregulation of autophagy markers including chaperone-mediated autophagy (CMA) substrate receptor LAMP-2 and lysosomal hydrolases Cathepsin S and Lysozyme. This suggests that lysosomal-mediated autophagy may be triggered in response to early rod apoptosis in Rpe65-LCA disease. These results highlight that Rpe65-related primary stress induces early signaling events, which trigger Bax-induced-apoptotic pathway and autophagy-mediated cellular response. These events may determine retinal cell fate, progression and severity of the disease.


Assuntos
Apoptose , Proteínas de Transporte/genética , Proteínas do Olho/genética , Regulação da Expressão Gênica/fisiologia , Amaurose Congênita de Leber/patologia , Proteína 2 de Membrana Associada ao Lisossomo/genética , Células Fotorreceptoras Retinianas Bastonetes/patologia , Animais , Autofagia , Western Blotting , Catepsinas/genética , Técnica Indireta de Fluorescência para Anticorpo , Técnicas de Genotipagem , Marcação In Situ das Extremidades Cortadas , Amaurose Congênita de Leber/genética , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BL , Camundongos Knockout , Muramidase/genética , Proteínas Proto-Oncogênicas c-bcl-2/genética , Reação em Cadeia da Polimerase em Tempo Real , Proteína X Associada a bcl-2/genética , cis-trans-Isomerases
5.
Invest Ophthalmol Vis Sci ; 52(8): 5933-40, 2011 Jul 29.
Artigo em Inglês | MEDLINE | ID: mdl-21715356

RESUMO

PURPOSE: To investigate the role of the myocyte enhancer factor 2 (Mef2) transcription factor family in retinal diseases, Mef2c expression was assessed during retinal degeneration in the Rpe65(-/-) mouse model of Leber's congenital amaurosis (LCA). Mef2c-dependent expression of photoreceptor-specific genes was further addressed. METHODS: Expression of Mef2 members was analyzed by oligonucleotide microarray, quantitative PCR (qPCR), and in situ hybridization. Mef2c-dependent transcriptional activity was assayed by luciferase assay in HEK293T cells. RESULTS: Mef2c was the only Mef2 member markedly downregulated during retinal degeneration in Rpe65(-/-) mice. Mef2c mRNA level was decreased by more than 2-fold at 2 and 4 months and by 3.5-fold at 6 months in retinas of Rpe65(-/-) mice. Downregulation of Mef2c at the protein level was confirmed in Rpe65(-/-) retinas. The decrease in Mef2c mRNA levels in the developing Rpe65(-/-) retinas from postnatal day (P) 13 onward was concomitant with the decreased expression of the rod-specific transcription factors Nrl and Nr2e3. Nrl was further shown to drive Mef2c transcriptional activity, supporting a physiological role for Mef2c in the retina. In addition, Mef2c appeared to act as a transcriptional repressor of its own expression and the expression of the retina-specific retinal G-protein coupled receptor (Rgr), rhodopsin, and M-opsin genes. CONCLUSIONS: These findings highlight the early altered regulation of the rod-specific transcriptional network in Rpe65-related disease. They also indicate that Mef2c may act as a novel transcription factor involved in the development and the maintenance of photoreceptor cells.


Assuntos
Proteínas de Transporte/genética , Proteínas do Olho/genética , Amaurose Congênita de Leber/genética , Fatores de Regulação Miogênica/genética , Degeneração Retiniana/genética , Células Fotorreceptoras Retinianas Bastonetes/fisiologia , Animais , Sequência de Bases , Fatores de Transcrição de Zíper de Leucina Básica/genética , Regulação para Baixo/fisiologia , Expressão Gênica/fisiologia , Células HEK293 , Humanos , Amaurose Congênita de Leber/fisiopatologia , Fatores de Transcrição MEF2 , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Mutantes , Dados de Sequência Molecular , Fatores de Regulação Miogênica/metabolismo , Análise de Sequência com Séries de Oligonucleotídeos , Receptores Nucleares Órfãos/genética , Regiões Promotoras Genéticas/fisiologia , RNA Mensageiro/metabolismo , Degeneração Retiniana/fisiopatologia , Células Fotorreceptoras Retinianas Bastonetes/metabolismo , Transcrição Gênica/fisiologia , cis-trans-Isomerases
6.
Mol Vis ; 17: 1287-97, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21633714

RESUMO

PURPOSE: In this study, we investigated the expression of the gene encoding ß-galactosidase (Glb)-1-like protein 3 (Glb1l3), a member of the glycosyl hydrolase 35 family, during retinal degeneration in the retinal pigment epithelium (RPE)-specific 65-kDa protein knockout (Rpe65(-/-)) mouse model of Leber congenital amaurosis (LCA). Additionally, we assessed the expression of the other members of this protein family, including ß-galactosidase-1 (Glb1), ß-galactosidase-1-like (Glb1l), and ß-galactosidase-1-like protein 2 (Glb1l2). METHODS: The structural features of Glb1l3 were assessed using bioinformatic tools. mRNA expression of Glb-related genes was investigated by oligonucleotide microarray, real-time PCR, and reverse transcription (RT) -PCR. The localized expression of Glb1l3 was assessed by combined in situ hybridization and immunohistochemistry. RESULTS: Glb1l3 was the only Glb-related member strongly downregulated in Rpe65(-/-) retinas before the onset and during progression of the disease. Glb1l3 mRNA was only expressed in the retinal layers and the RPE/choroid. The other Glb-related genes were ubiquitously expressed in different ocular tissues, including the cornea and lens. In the healthy retina, expression of Glb1l3 was strongly induced during postnatal retinal development; age-related increased expression persisted during adulthood and aging. CONCLUSIONS: These data highlight early-onset downregulation of Glb1l3 in Rpe65-related disease. They further indicate that impaired expression of Glb1l3 is mostly due to the absence of the chromophore 11-cis retinal, suggesting that Rpe65 deficiency may have many metabolic consequences in the underlying neuroretina.


Assuntos
Proteínas de Transporte/genética , Modelos Animais de Doenças , Proteínas do Olho/genética , Glicosídeo Hidrolases/metabolismo , Amaurose Congênita de Leber/metabolismo , Camundongos , Epitélio Pigmentado da Retina/metabolismo , Envelhecimento/metabolismo , Animais , Animais Recém-Nascidos/crescimento & desenvolvimento , Animais Recém-Nascidos/metabolismo , Corioide/metabolismo , Progressão da Doença , Regulação para Baixo , Expressão Gênica , Glicosídeo Hidrolases/genética , Imuno-Histoquímica , Hibridização In Situ , Camundongos Endogâmicos C57BL , Camundongos Knockout/genética , RNA/metabolismo , RNA Mensageiro/metabolismo , Degeneração Retiniana/genética , Degeneração Retiniana/metabolismo , Retinaldeído/deficiência , cis-trans-Isomerases
7.
PLoS One ; 4(8): e6616, 2009 Aug 12.
Artigo em Inglês | MEDLINE | ID: mdl-19672311

RESUMO

Pathogenesis in the Rpe65(-/-) mouse model of Leber's congenital amaurosis (LCA) is characterized by a slow and progressive degeneration of the rod photoreceptors. On the opposite, cones degenerate rapidly at early ages. Retinal degeneration in Rpe65(-/-) mice, showing a null mutation in the gene encoding the retinal pigment epithelium 65-kDa protein (Rpe65), was previously reported to depend on continuous activation of a residual transduction cascade by unliganded opsin. However, the mechanisms of apoptotic signals triggered by abnormal phototransduction remain elusive. We previously reported that activation of a Bcl-2-dependent pathway was associated with apoptosis of rod photoreceptors in Rpe65(-/-) mice during the course of the disease. In this study we first assessed whether activation of Bcl-2-mediated apoptotic pathway was dependent on constitutive activation of the visual cascade through opsin apoprotein. We then challenged the direct role of pro-apoptotic Bax protein in triggering apoptosis of rod and cone photoreceptors.Quantitative PCR analysis showed that increased expression of pro-apoptotic Bax and decreased level of anti-apoptotic Bcl-2 were restored in Rpe65(-/-)/Gnat1(-/-) mice lacking the Gnat1 gene encoding rod transducin. Moreover, photoreceptor apoptosis was prevented as assessed by TUNEL assay. These data indicate that abnormal activity of opsin apoprotein induces retinal cell apoptosis through the Bcl-2-mediated pathway. Following immunohistological and real-time PCR analyses, we further observed that decreased expression of rod genes in Rpe65-deficient mice was rescued in Rpe65(-/-)/Bax(-/-) mice. Histological and TUNEL studies confirmed that rod cell demise and apoptosis in diseased Rpe65(-/-) mice were dependent on Bax-induced pathway. Surprisingly, early loss of cones was not prevented in Rpe65(-/-)/Bax(-/-) mice, indicating that pro-apoptotic Bax was not involved in the pathogenesis of cone cell death in Rpe65-deficient mice.This is the first report, to our knowledge, that a single genetic mutation can trigger two independent apoptotic pathways in rod and cone photoreceptors in Rpe65-dependent LCA disease. These results highlight the necessity to investigate and understand the specific death signaling pathways committed in rods and cones to develop effective therapeutic approaches to treat RP diseases.


Assuntos
Apoptose/fisiologia , Amaurose Congênita de Leber/patologia , Células Fotorreceptoras Retinianas Cones/patologia , Doenças Retinianas/patologia , Células Fotorreceptoras Retinianas Bastonetes/patologia , Proteína X Associada a bcl-2/fisiologia , Animais , Proteínas de Transporte/genética , Proteínas de Transporte/fisiologia , Proteínas do Olho/genética , Proteínas do Olho/fisiologia , Subunidades alfa de Proteínas de Ligação ao GTP/genética , Subunidades alfa de Proteínas de Ligação ao GTP/fisiologia , Amaurose Congênita de Leber/complicações , Camundongos , Camundongos Knockout , Transducina/genética , Transducina/fisiologia , Visão Ocular , Proteína X Associada a bcl-2/genética , cis-trans-Isomerases
8.
Curr Mol Med ; 9(3): 375-83, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19355918

RESUMO

Mutations in humans are associated with several forms of inherited retinal dystrophies, such as Retinitis Pigmentosa which lead to retinal cell death and irreversible loss of vision. Genes involved in affected patients mainly encode proteins related to vision physiology including visual cycle and light-dependent phototransduction cascade. As reported in spontaneous and genetically engineered mouse models, apoptosis is a common fate in retinal degeneration, although the triggered signals to retinal apoptosis remain largely unraveled. Several studies highlighted that many of the molecular pathways involved in ocular diseases rely on caspase-dependent or -independent apoptotic mitochondrial pathway involving the Bcl-2 family of proteins. Anti- and pro-apoptotic Bcl-2 members are present in retinal tissues and are thought to play a role in the pathogenesis of several retinal disorders. Since almost no efficient treatments are available so far, it remains a great challenge to decipher the molecular pathways involved in retinal dystrophies and to develop alternative therapies to prevent or inhibit eye defect. Toward this goal, mutation-independent strategies such as molecular therapy provides promising and exciting approaches to deliver anti-apoptotic molecules targeting the Bcl-2 pathway through the use of cell permeable transport peptides. Modulation of common apoptotic signaling pathways may be of outstanding potential to target multiple retinal dystrophies regardless of the primary genetic defect.


Assuntos
Apoptose/fisiologia , Retinose Pigmentar/patologia , Retinose Pigmentar/fisiopatologia , Animais , Caspases/metabolismo , Humanos , Transdução de Sinal Luminoso/fisiologia , Mutação , Retinose Pigmentar/genética , Transdução de Sinais/fisiologia
9.
Mol Vis ; 14: 2126-35, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-19050768

RESUMO

PURPOSE: An increased mRNA expression of the genes coding for the extracellular matrix proteins neuroglycan C (NGC), interphotoreceptor matrix proteoglycan 2 (IMPG2), and CD44 antigen (CD44) has been observed during retinal degeneration in mice with a targeted disruption of the Rpe65 gene (Rpe65-/- mouse). To validate these data, we analyzed this differential expression in more detail by characterizing retinal NGC mRNA isoform and protein expression during disease progression. METHODS: Retinas from C57/Bl6 wild-type and Rpe65-/- mice, ranging 2 to 18 months of age, were used. NGC, IMPG2, and CD44 mRNA expression was assessed by oligonucleotide microarray, quantitative PCR, and in situ hybridization. Retinal NGC protein expression was analyzed by western blot and immunohistochemistry. RESULTS: As measured by quantitative PCR, mRNA expression of NGC and CD44 was induced by about 2 fold to 3 fold at all time points in Rpe65-/- retinas, whereas initially 4 fold elevated IMPG2 mRNA levels progressively declined. NGC and IMPG2 mRNAs were expressed in the ganglion cell layer, the inner nuclear layer, and at the outer limiting membrane. NGC mRNA was also detected in retinal pigment epithelium cells (RPE), where its mRNA expression was not induced during retinal degeneration. NGC-I was the major isoform detected in the retina and the RPE, whereas NGC-III was barely detected and NGC-II could not be assessed. NGC protein expression was at its highest levels on the apical membrane of the RPE. NGC protein levels were induced in retinas from 2- and 4-month-old Rpe65-/- mice, and an increased amount of the activity-cleaved NGC ectodomain containing an epidermal growth factor (EGF)-like domain was detected. CONCLUSIONS: During retinal degeneration in Rpe65-/- mice, NGC expression is induced in the neural retina, but not in the RPE, where NGC is expressed at highest levels.


Assuntos
Proteínas de Transporte/metabolismo , Proteínas do Olho/metabolismo , Proteínas de Membrana/metabolismo , Proteoglicanas/metabolismo , Degeneração Retiniana/metabolismo , Animais , Proteínas de Transporte/genética , Progressão da Doença , Proteínas do Olho/genética , Proteínas de Membrana/genética , Camundongos , Camundongos Knockout , Isoformas de Proteínas/genética , Proteoglicanas/genética , RNA Mensageiro/metabolismo , Retina/metabolismo , Degeneração Retiniana/fisiopatologia , Distribuição Tecidual , Regulação para Cima , cis-trans-Isomerases
10.
Apoptosis ; 13(3): 329-42, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18274907

RESUMO

Mutations in RPE65 protein is characterized by the loss of photoreceptors, although the molecular pathways triggering retinal cell death remain largely unresolved. The role of the Bcl-2 family of proteins in retinal degeneration is still controversial. However, alteration in Bcl-2-related proteins has been observed in several models of retinal injury. In particular, Bax has been suggested to play a crucial role in apoptotic pathways in murine glaucoma model as well as in retinal detachment-associated cell death. We demonstrated that Bcl-2-related signaling pathway is involved in Rpe65-dependent apoptosis of photoreceptors during development of the disease. Pro-apoptotic Bax alpha and beta isoforms were upregulated in diseased retina. This was associated with a progressive reduction of anti-apoptotic Bcl-2, reflecting imbalanced Bcl-2/Bax ratio as the disease progresses. Moreover, specific translocation of Bax beta from cytosol to mitochondria was observed in Rpe65-deficient retina. This correlated with the initiation of photoreceptor cell loss at 4 months of age, and further increased during disease development. Altogether, these data suggest that Bcl-2-apoptotic pathway plays a crucial role in Leber's congenital amaurosis disease. They further highlight a new regulatory mechanism of Bax-dependent apoptosis based on regulated expression and activation of specific isoforms of this protein.


Assuntos
Apoptose/fisiologia , Cegueira/genética , Proteínas de Transporte/genética , Proteínas do Olho/genética , Células Fotorreceptoras/citologia , Proteínas Proto-Oncogênicas c-bcl-2/fisiologia , Retina/metabolismo , Proteína X Associada a bcl-2/fisiologia , Animais , Cegueira/congênito , Cegueira/fisiopatologia , Linhagem Celular , Modelos Animais de Doenças , Regulação da Expressão Gênica , Humanos , Marcação In Situ das Extremidades Cortadas , Camundongos , Mitocôndrias/metabolismo , Conformação Proteica , Transporte Proteico , Regulação para Cima , Proteína X Associada a bcl-2/biossíntese , cis-trans-Isomerases
11.
Arch Ophthalmol ; 125(2): 231-6, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17296900

RESUMO

OBJECTIVE: To evaluate visual function in 2 boys and their maternal aunt affected with Danon disease due to a mutation in the X-linked lysosome-associated membrane protein-2 (LAMP2) gene. METHODS: Linkage analysis using microsatellite markers from the X chromosome was done in family members from the paternal side. Visual acuity testing, fundus analysis, fluorescence angiography, and full-field electroretinography were performed in all 3 patients. RESULTS: Eye examinations confirmed the presence of retinopathy in the 2 boys and their maternal aunt, obligate carrier for the S157X mutation in LAMP2. The expression of the disease was milder in the female carrier than in the hemizygous boys, possibly due to lyonization. CONCLUSIONS: Our report further expands the phenotype of Danon disease by describing retinopathy in 3 cases. A thorough clinical examination, including ophthalmic investigation, is needed in all cases of Danon disease. CLINICAL RELEVANCE: LAMP2 belongs to a growing number of retinopathy genes. Genes involved in systemic diseases associated with poor survival may see their effect in other organs, not only in the eyes, becoming a major source of concern once a good and reliable therapy is available. This also represents a major issue for genetic counseling for patients undergoing gene therapy in the future.


Assuntos
Doença de Depósito de Glicogênio Tipo IIb/genética , Proteínas de Membrana Lisossomal/genética , Mutação , Doenças Retinianas/genética , Adolescente , Cromossomos Humanos X/genética , Eletrorretinografia , Feminino , Angiofluoresceinografia , Ligação Genética , Heterozigoto , Humanos , Proteína 2 de Membrana Associada ao Lisossomo , Masculino , Repetições de Microssatélites/genética , Pessoa de Meia-Idade , Linhagem , Fenótipo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Irmãos , Acuidade Visual
12.
FASEB J ; 20(12): 2036-49, 2006 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-17012256

RESUMO

RPE65 is the retinal isomerase essential for conversion of all-trans-retinyl ester to 11-cis-retinol in the visual cycle. Leber's congenital amaurosis (LCA), an autosomal recessive form of RP resulting in blindness, is commonly caused by mutations in the Rpe65 gene. Whereas the molecular mechanisms by which these mutations contribute to retinal disease remain largely unresolved, affected patients show marked RPE damage and photoreceptor degeneration. We evaluated gene expression in Rpe65-/- mouse model of LCA before and at the onset of photoreceptor cell death in 2, 4, and 6 month old animals. Microarray analysis demonstrates altered expression of genes involved in phototransduction, apoptosis regulation, cytoskeleton organization, and extracellular matrix (ECM) constituents. Cone-specific phototransduction genes are strongly decreased, reflecting early loss of cones. In addition, remaining rods show modified expression of genes encoding components of the cytoskeleton and ECM. This may affect rod physiology and interaction with the adjacent RPE and lead to loss of survival signals, as reflected by the alteration of apoptosis-related genes Together, these results suggest that RPE65 defect triggers an overall remodeling of the neurosensitive retina that may, in turn, disrupt photoreceptor homeostasis and induce apoptosis signaling cascade toward retinal cell death.


Assuntos
Cegueira/genética , Proteínas do Olho/genética , Regulação da Expressão Gênica , Animais , Apoptose/genética , Cegueira/etiologia , Cegueira/patologia , Proteínas de Transporte , Proteínas do Citoesqueleto/genética , Modelos Animais de Doenças , Progressão da Doença , Proteínas da Matriz Extracelular/genética , Perfilação da Expressão Gênica , Camundongos , Camundongos Knockout , Análise de Sequência com Séries de Oligonucleotídeos , Células Fotorreceptoras/patologia , Visão Ocular/genética , cis-trans-Isomerases/genética
13.
J Biol Chem ; 277(37): 33978-86, 2002 Sep 13.
Artigo em Inglês | MEDLINE | ID: mdl-12058029

RESUMO

Molecular dissection of the mechanisms underlying Helicobacter pylori infection suffers from the lack of in vitro systems mimicking in vivo observations. A system was developed whereby human epithelial cells (Caco-2) grown as polarized monolayers and bacteria can communicate with each other under culture conditions optimal for each partner. Caco-2 cells grown on filter supports were inserted in a vertical position into diffusion chambers equilibrated with air and 5% CO(2) at their basolateral surface (aerophilic conditions) and 5% CO(2), 5% O(2), 90% N(2) (microaerophilic conditions) in the apical compartment. Remarkably, the epithelial polarized layer was stable under these asymmetric culture conditions for at least 24 h, and the presence of Caco-2 cells was necessary to maintain H. pylori growth. In contrast to previous studies conducted with non-polarized Caco-2 cells and other cell lines kept under aerophilic conditions, we found H. pylori-dependent stimulation of cytokine secretion (MCP-1 (monocyte chemoattractant protein-1), GRO-alpha (growth-regulated oncogene-alpha), RANTES (regulated on activation normal T cell expressed and secreted)). This correlated with nuclear translocation of NF-kappaB p50 and p65 subunits. Tyrosine phosphorylation of nine cellular proteins was induced or enhanced; we identified p120(RasGAP), p190(RhoGAP), p62dok (downstream of tyrosine kinases), and cortactin as H. pylori-inducible targets. Moreover, reduction of H. pylori urease expression was observed in adherent bacteria as compared with bacteria in suspension. In addition to mimicking several observations seen in the inflamed gastric mucosa, the novel in vitro system was allowed to underscore complex cellular events not seen in classical in vitro analyses of microaerophilic bacteria-epithelial cell cross-talk.


Assuntos
Proteínas de Ligação a DNA/metabolismo , Fatores de Troca do Nucleotídeo Guanina/metabolismo , Infecções por Helicobacter/metabolismo , Helicobacter pylori , Proteínas dos Microfilamentos/metabolismo , Proteínas Nucleares/metabolismo , Fosfoproteínas/metabolismo , Proteínas de Ligação a RNA/metabolismo , Proteína p120 Ativadora de GTPase/metabolismo , Células CACO-2 , Polaridade Celular , Quimiocinas/metabolismo , Cortactina , Células Epiteliais/metabolismo , Proteínas Ativadoras de GTPase , Mucosa Gástrica/metabolismo , Helicobacter pylori/enzimologia , Helicobacter pylori/crescimento & desenvolvimento , Humanos , NF-kappa B/metabolismo , Fosforilação , Proteínas Repressoras , Urease/biossíntese , ras-GRF1
14.
Diabetes ; 51(6): 1805-14, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12031968

RESUMO

Type 1 diabetes is characterized by the infiltration of activated leukocytes within the pancreatic islets, leading to beta-cell dysfunction and destruction. The exact role played by interferon-gamma, tumor necrosis factor (TNF)-alpha, and interleukin-1beta in this pathogenic process is still only partially understood. To study cytokine action at the cellular level, we are working with the highly differentiated insulin-secreting cell line, betaTc-Tet. We previously reported that it was susceptible to apoptosis induced by TNF-alpha, in combination with interleukin-1beta and interferon-gamma. Here, we report that cytokine-induced apoptosis was correlated with the activation of caspase-8. We show that in betaTc-Tet cells, overexpression of cFLIP, the cellular FLICE (FADD-like IL-1beta-converting enzyme)-inhibitory protein, completely abolished cytokine-dependent activation of caspase-8 and protected the cells against apoptosis. Furthermore, cFLIP overexpression increased the basal and interleukin-1beta-mediated transcriptional activity of nuclear factor (NF)-kappaB, whereas it did not change cytokine-induced inducible nitric oxide synthase gene transcription and nitric oxide secretion. The presence of cFLIP prevented the weak TNF-alpha-induced reduction in cellular insulin content and secretion; however, it did not prevent the decrease in glucose-stimulated insulin secretion induced by the combined cytokines, in agreement with our previous data demonstrating that interferon-gamma alone could induce these beta-cell dysfunctions. Together, our data demonstrate that overexpression of cFLIP protects mouse beta-cells against TNF-alpha-induced caspase-8 activation and apoptosis and is correlated with enhanced NF-kappaB transcriptional activity, suggesting that cFLIP may have an impact on the outcome of death receptor-triggered responses by directing the intracellular signals from beta-cell death to beta-cell survival.


Assuntos
Apoptose , Proteínas de Transporte/fisiologia , Caspases/metabolismo , Insulina/metabolismo , Peptídeos e Proteínas de Sinalização Intracelular , Ilhotas Pancreáticas/metabolismo , Fator de Necrose Tumoral alfa/farmacologia , Animais , Proteína Reguladora de Apoptosis Semelhante a CASP8 e FADD , Proteínas de Transporte/genética , Caspase 8 , Caspase 9 , Linhagem Celular , Ativação Enzimática/efeitos dos fármacos , Expressão Gênica , Glucose/farmacologia , Humanos , Secreção de Insulina , Interferon gama/farmacologia , Interleucina-1/farmacologia , Ilhotas Pancreáticas/citologia , Camundongos , Camundongos Transgênicos , NF-kappa B/metabolismo , Óxido Nítrico/metabolismo , Óxido Nítrico Sintase/genética , Óxido Nítrico Sintase Tipo II , Proteínas Recombinantes , Transcrição Gênica , Transfecção
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