Persistent hyperplastic primary vitreous in transgenic mice expressing IE180 of the pseudorabies virus

Investigative Ophthalmology and Visual Science

Volumn 46, Issue 5, 2005, Pages 1551-1556

  Taharaguchi, Satoshi ^a,c   Yoshida, Kazuhiko ^b   Tomioka, Yukiko ^a   Yoshino, Saori ^a,d   Uede, Toshimitsu ^a   Ono, Etsuro ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

^c KAGOSHIMA UNIVERSITY   (Japan)

^d Gene Techno Science   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BROXURIDINE; CD31 ANTIGEN; ENDOGLIN ANTIBODY; EOSIN; HEMATOXYLIN; PROTEIN ANTIBODY; PROTEIN IE180; UNCLASSIFIED DRUG; VASCULOTROPIN ANTIBODY; VIRUS PROTEIN; BIOLOGICAL MARKER; IMMEDIATE EARLY PROTEIN; PSEUDORABIES VIRUS IMMEDIATE EARLY PROTEINS;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL PROLIFERATION; CONTROLLED STUDY; ENDOTHELIUM CELL; EYE DEVELOPMENT; HISTOPATHOLOGY; IMMUNOCYTOCHEMISTRY; LEUKOKORIA; MELANOCYTE; MOUSE; NERVE CELL; NONHUMAN; PERINATAL PERIOD; PERSISTENT HYPERPLASTIC PRIMARY VITREOUS; PHOTORECEPTOR; PRIORITY JOURNAL; PROTEIN EXPRESSION; PSEUDORABIES HERPETOVIRUS; PUPIL; RETINA; STAINING; TRANSGENIC MOUSE; ANIMAL; C3H MOUSE; C57BL MOUSE; CONGENITAL MALFORMATION; DISEASE MODEL; EYE MALFORMATION; FLUORESCENCE MICROSCOPY; GENE EXPRESSION; HYPERPLASIA; IMMUNOHISTOCHEMISTRY; METABOLISM; PATHOLOGY; PHYSIOLOGY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TRANSGENE; VASCULARIZATION; VITREOUS BODY;

ANIMALS; BIOLOGICAL MARKERS; CELL PROLIFERATION; DISEASE MODELS, ANIMAL; EYE ABNORMALITIES; GENE EXPRESSION; HERPESVIRUS 1, SUID; HYPERPLASIA; IMMEDIATE-EARLY PROTEINS; IMMUNOHISTOCHEMISTRY; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; MICE, TRANSGENIC; MICROSCOPY, FLUORESCENCE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TRANSGENES; VITREOUS BODY;

EID: 20444504697     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: 10.1167/iovs.04-0743     Document Type: Article

References (40)

1. Reese AB. Persistent hyperplastic primary vitreous. Am J Ophthalmol. 1955;40:317-331.
2. Kaste SC, Jenkins JJ III, Meyer D, Fontanesi J, Pratt CB. Persistent hyperplastic primary vitreous of the eye: imaging findings with pathologic correlation. AJR Am J Roentgenol. 1994;162:437-440.
3. Wells RG, Miro P, Brummond R. Color-flow Doppler sonography of persistent hyperplastic primary vitreous. J Ultrasound Med. 1991;10:405-407.
4. Pruett RC, Schepens CL. Posterior hyperplastic primary vitreous. Am J Ophthalmol. 1970;69:534-543.
5. Goldberg MF. Persistent fetal vasculature (PFV): an integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture. Am J Ophthalmol. 1997;124:587-626.
6. Kit S. Pseudorabies virus. Webster RG, Granoff A, eds. Encyclopedia of Virology. London: Academic Press; 1994.
7. Schneider WJ. Viral pathogenesis during experimental pseudorabies keratoconjunctivitis in the pig. J Infect Dis. 1973;128:598-604.
8. Schneider WJ, Howarth JA. Clinical course and histopathologic features of pseudorabies virus-induced keratoconjunctivitis in pigs. Am J Vet Res. 1973;34:393-401.
9. Howarth JA, De Paoli A. An enzootic of pseuodorabies in swain in California. J Am Vet Med Assoc. 1968;152:1114-1118.
10. Kritas SK, Pensaert MB. Role of gp63 and gIII of Aujeszky's disease virus in the invasion of the olfactory nervous pathway in neonatal pigs. Acta Vet Hung. 1994;42:309-316.
11. Kritas SK, Pensaert MB, Mettenleiter TC. Invasion and spread of single glycoprotein deleted mutants of Aujeszky's disease virus (ADV) in the trigeminal nervous pathway of pigs after intranasal inoculation. Vet Microbiol. 1994;40:323-334.
12. Green MR, Treisman R, Maniatis T. Transcriptional activation of cloned human beta-globin genes by viral immediate-early gene products. Cell. 1983;35:137-l48.
13. Ihara S, Feldman L, Watanabe S, Ben-Porat T. Characterization of the immediate-early functions of pseudorabies virus. Virology. 1983;131:437-454.
14. Wu L, Berk AJ. Transcriptional activation by the pseudorabies virus immediate early protein requires the TATA box element in the adenovirus 2 E1B promoter. Virology. 1988;167:318-322.
15. Wong ML, Ho TY, Huang JH, Hsiang CY, Chang TJ. Stimulation of type I DNA topoisomerase gene expression by pseudorabies virus. Arch Virol. 1997;142:2099-2105.
16. Yuan R, Bohan C, Shiao FC, et al. Activation of HIV LTR-directed expression: analysis with pseudorabies virus immediate early gene. Virology. 1989;172:92-99.
17. Cromlish WA, Abmayr SM, Workman JL, Horikoshi M, Roeder RG. Transcriptionally active immediate-early protein of pseudorabies virus binds to specific sites on class II gene promoters. J Virol. 1989;63:1869-1876.
18. Chlan CA, Coulter C, Feldman LT. Binding of the pseudorabies virus immediate-early protein to single-stranded DNA. J Virol. 1987;61:1855-1860.
19. Taharaguchi S, Kon Y, Yoshino S, Ono E. Impaired development of the cerebellum in transgenic mice expressing the immediate-early protein IE180 of pseudorabies virus. Virology. 2003;307:243-254.
20. Sakai M, Serria MS, Ikeda H, et al. Regulation of c-maf gene expression by Pax6 in cultured cells. Nucleic Acids Res. 2001;29:1228-1237.
21. Sakai MIJ, Yoshida K, Ogata A, et al. Rat maf related genes: specific expression in chondrocytes, lens and spinal cord. Oncogene. 1997;14:745-750.
22. Yoshida K, Hu Y, Karin M. IκB kinase alpha is essential for development of the mammalian cornea and conjunctiva. Invest Ophthalmol Vis Sci. 2000;41:3665-3669.
23. Yoshida K, Imaki J, Koyama Y, et al. Differential expression of maf-1 and maf-2 genes in the developing rat lens. Invest Ophthalmol Vis Sci. 1997;38:2679-2683.
24. Yoshida K, Kini JI, Imaki J, et al. Proliferation in the posterior region of the lens of c-maf-/- mice. Curr Eye Res. 2001;23:116-119.
25. Hogan BF, Constantin F, Kacy E. Manipulating the Mouse Embryo. A Laboratory Manual. New York: Cold Spring Harbor Laboratory Press; 1986:153-163.
26. Ono E, Tasaki T, Kobayashi T, et al. Resistance to pseudorabies virus infection in transgenic mice expressing the chimeric transgene that represses the immediate-early gene transcription. Virology. 1999;262:72-78.
27. Jones BJ, Roberts DJ. A rotarod suitable for quantitative measurements of motor incoordination in naive mice. Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1968;259:211.
28. Dean PN, Dolbeare F, Gratzner H, Rice GC, Gray JW. Cell-cycle analysis using a monoclonal antibody to BrdUrd. Cell Tissue Kinet. 1984;17:427-436.
29. Dolbeare F, Gratzner H, Pallavicini MG, Gray JW. Flow cytometric measurement of total DNA content and incorporated bromodeoxyuridine. Proc Natl Acad Sci USA. 1983;80:5573-5577.
30. Nowakowski RS, Lewin SB, Miller MW. Bromodeoxyuridine immunohistochemical determination of the lengths of the cell cycle and the DNA-synthetic phase for an anatomically defined population. J Neurocytol. 1989;18:311-318.
31. Yoshiki A, Hanazono M, Oda S, et al. Developmental analysis of the eye lens obsolescence (Elo) gene in the mouse: cell proliferation and Elo gene expression in the aggregation chimera. Development. 1991;113:1293-1304.
32. Chang YS, di Tomaso E, McDonald DM, et al. Mosaic blood vessels in tumors: frequency of cancer cells in contact with flowing blood. Proc Natl Acad Sci USA. 2000;97:14608-14613.
33. Ozerdem U, Stallcup WB. Early contribution of pericytes to angiogenic sprouting and tube formation. Angiogenesis. 2003;6:241-249.
34. Ito M, Yoshioka M. Regression of the hyaloid vessels and pupillary membrane of the mouse. Anat Embryol (Berl). 1999;200:403-411.
35. Haddad R, Font RL, Reeser F. Persistent hyperplastic primary vitreous: a clinicopathologic study of 62 cases and review of the literature. Surv Ophthalmol. 1978;23:123-134.
36. Matsuo T. The genes involved in the morphogenesis of the eye. Jpn J Ophthalmol. 1993;37:215-251.
37. Beauchamp GR, Knepper PA. Role of the neural crest in anterior segment development and disease. J Pediatr Ophthalmol Strabismus. 1984;21:209-214.
38. Noden DM. Periocular mesenchyme: neural crest and mesodermal interactions. In: Tasman W, Jaeger EA, eds. Foundations of Clinical Ophthalmology. Philadelphia: JB Lippincott; 1991:1-23.
39. Etchevers HC, Vincent C, Le Douarin NM, Couly GF. The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain. Development. 2001;128:1059-1068.
40. Korn J, Christ B, Kurz H. Neuroectodermal origin of brain pericytes and vascular smooth muscle cells. J Comp Neurol. 2002;442:78-88.