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1.
Case Rep Ophthalmol Med ; 2023: 5693657, 2023.
Article in English | MEDLINE | ID: mdl-37920747

ABSTRACT

We report a case of a 9-year-old girl presenting with unilateral retinal arteriovenous malformation (AVM) with symptomatic macular edema. Over 5 years of follow-up includes optical coherence tomography (OCT), fundus photographs, and fluorescein angiography at baseline and at follow-up. Systemic and neurologic workup was completed and negative for intracranial AVM. Vision has correlated with macular edema, ranging from 20/20 to 20/80. The patient has received nine injections of intravitreal bevacizumab and has not required an injection for the last couple of years. Follow-up is ongoing.

2.
Sci Rep ; 8(1): 16967, 2018 11 16.
Article in English | MEDLINE | ID: mdl-30446707

ABSTRACT

Photoreceptor cells are specialized neurons with a sensory cilium carrying an elaborate membrane structure, the outer segment (OS). Inherited mutations in genes involved in ciliogenesis frequently result in OS malformation and blindness. ADP-ribosylation factor-like 2 (ARL2) has recently been implicated in OS formation through its association with Binder of ARL2 (BART or ARL2BP), a protein linked to inherited blinding disease. To test the role of ARL2 in vision we created a transgenic mouse model expressing a tagged-dominant active form of human ARL2 (ARL2-Q70L) under a rod-specific promoter. Transgenic ARL2-Q70L animals exhibit reduced photoreceptor cell function as early as post-natal day 16 and progressive rod degeneration. We attribute loss of photoreceptor function to the defective OS morphogenesis in the ARL2-Q70L transgenic model. ARL2-Q70L expression results in shortened inner and outer segments, shortened and mislocalized axonemes and cytoplasmic accumulation of rhodopsin. In conclusion, we show that ARL2-Q70L is crucial for photoreceptor neuron sensory cilium development. Future research will expand upon our hypothesis that ARL2-Q70L mutant interferes with microtubule maintenance and tubulin regulation resulting in impaired growth of the axoneme and elaboration of the photoreceptor outer segment.


Subject(s)
Cilia/physiology , GTP-Binding Proteins/metabolism , Retinal Neurons/metabolism , Retinal Rod Photoreceptor Cells/metabolism , Rod Cell Outer Segment/metabolism , Animals , Axoneme/metabolism , Cell Line , Cilia/genetics , Female , GTP-Binding Proteins/genetics , Humans , Mice , Mice, Transgenic , Mutation, Missense , Rhodopsin/metabolism
3.
Hum Mol Genet ; 25(10): 2031-2044, 2016 05 15.
Article in English | MEDLINE | ID: mdl-26936825

ABSTRACT

The small GTPase, ADP-ribosylation factor-like 3 (ARL3), has been proposed to participate in the transport of proteins in photoreceptor cells. Moreover, it has been implicated in the pathogenesis associated with X-linked retinitis pigmentosa (XLRP) resulting from mutations in the ARL3 GTPase activating protein, retinitis pigmentosa 2 (RP2). To determine the importance of ARL3 in rod photoreceptor cells, we generated transgenic mice expressing a dominant active form of ARL3 (ARL3-Q71L) under a rod-specific promoter. ARL3-Q71L animals exhibited extensive rod cell death after post-natal day 30 (PN30) and degeneration was complete by PN70. Prior to the onset of cell death, rod photoresponse was significantly reduced along with a robust decrease in rod phosphodiesterase 6 (PDE6) and G-protein receptor kinase-1 (GRK1) levels. Furthermore, assembled phosphodiesterase-6 (PDE6) subunits, rod transducin and G-protein receptor kinase-1 (GRK1) accumulated on large punctate structures within the inner segment in ARL3-Q71L retina. Defective trafficking of prenylated proteins is likely due to sequestration of prenyl binding protein δ (PrBPδ) by ARL3-Q71L as we demonstrate a specific interaction between these proteins in the retina. Unexpectedly, our studies also revealed a novel role for ARL3 in the migration of photoreceptor nuclei. In conclusion, this study identifies ARL3 as a key player in prenylated protein trafficking in rod photoreceptor cells and establishes the potential role for ARL3 dysregulation in the pathogenesis of RP2-related forms of XLRP.


Subject(s)
ADP-Ribosylation Factors/genetics , Genetic Diseases, X-Linked/genetics , Pyrophosphatases/genetics , Retinitis Pigmentosa/genetics , ADP-Ribosylation Factors/biosynthesis , Animals , Cyclic Nucleotide Phosphodiesterases, Type 6/biosynthesis , Cyclic Nucleotide Phosphodiesterases, Type 6/genetics , Eye Proteins/biosynthesis , Eye Proteins/genetics , G-Protein-Coupled Receptor Kinase 1/biosynthesis , G-Protein-Coupled Receptor Kinase 1/genetics , GTP-Binding Proteins , Gene Expression Regulation , Genetic Diseases, X-Linked/pathology , Humans , Membrane Proteins , Mice , Mice, Transgenic , Protein Prenylation/genetics , Retina/metabolism , Retina/pathology , Retinal Rod Photoreceptor Cells/metabolism , Retinal Rod Photoreceptor Cells/pathology , Retinitis Pigmentosa/pathology , Rod Cell Outer Segment/metabolism , Rod Cell Outer Segment/pathology
4.
Annu Rev Chem Biomol Eng ; 4: 143-70, 2013.
Article in English | MEDLINE | ID: mdl-23540287

ABSTRACT

Environmental concerns have led to the development of biorenewable polymers with the ambition to utilize them at an industrial scale. Poly(lactic acid) and poly(hydroxyalkanoates) are semicrystalline, biorenewable polymers that have been identified as the most promising alternatives to conventional plastics. However, both are inherently susceptible to brittleness and degradation during thermal processing; we discuss several approaches to overcome these problems to create a balance between durability and biodegradability. For example, copolymers and blends can increase ductility and the thermal-processing window. Furthermore, chain modifications (e.g., branching/crosslinking), processing techniques (fiber drawing/annealing), or additives (plasticizers/nucleating agents) can improve mechanical properties and prevent thermal degradation during processing. Finally, we examine the impacts of morphology on end-of-life degradation to complete the picture for the most common renewable polymers.


Subject(s)
Lactic Acid/chemistry , Models, Chemical , Plastics/chemistry , Polymers/chemistry , Polyesters
5.
Bioinformatics ; 25(7): 974-6, 2009 Apr 01.
Article in English | MEDLINE | ID: mdl-18326507

ABSTRACT

UNLABELLED: MiSearch is an adaptive biomedical literature search tool that ranks citations based on a statistical model for the likelihood that a user will choose to view them. Citation selections are automatically acquired during browsing and used to dynamically update a likelihood model that includes authorship, journal and PubMed indexing information. The user can optionally elect to include or exclude specific features and vary the importance of timeliness in the ranking. AVAILABILITY: http://misearch.ncibi.org. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.


Subject(s)
PubMed , Software , Algorithms , Computational Biology/methods , Databases, Factual , Information Storage and Retrieval/methods , Internet , User-Computer Interface
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