Involvement of claudins in zebrafish brain ventricle morphogenesis

Annals of the New York Academy of Sciences

Volumn 1257, Issue 1, 2012, Pages 193-198

  Zhang, Jingjing ^a,b   Liss, Martin ^a   Wolburg, Hartwig ^c   Blasig, Ingolf E ^d   Abdelilah Seyfried, Salim ^a  

^a MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^b GUANGDONG MEDICAL UNIVERSITY   (China)

^c UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

^d LEIBNIZ INSTITUT FÜR MOLEKULARE PHARMAKOLOGIE   (Germany)

Author keywords

Brain ventricle morphogenesis; Claudin 3; Claudin 5a; Tight junction

Indexed keywords

CLAUDIN 3; CLAUDIN 5;

BLOOD BRAIN BARRIER; BRAIN DEVELOPMENT; BRAIN VENTRICLE; CONTROLLED STUDY; EMBRYO DEVELOPMENT; ENDOTHELIUM CELL; HYDROSTATIC PRESSURE; MICROVASCULATURE; MORPHOGENESIS; NONHUMAN; PROTEIN EXPRESSION; PROTEIN FUNCTION; REVIEW; ZEBRA FISH;

DANIO RERIO; MAMMALIA;

EID: 84861992025     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2012.06507.x     Document Type: Review

References (30)

1. Cushing, H. 1914. Studies on the cerebrospinal fluid. I. Introduction. J. Med. Res. 26: 1-19.
2. Milhorat, T.H., M.K. Hammock, J.D. Fenstermacher & V.A. Levin. 1971. Cerebrospinal fluid production by the choroid plexus and brain. Science 173: 330-332.
3. Pollay, M. & F. Curl. 1967. Secretion of cerebrospinal fluid by the ventricular ependyma of the rabbit. Am. J. Physiol. 213: 1031-1038.
4. Davson, H. & M.B. Segal. 1996. Physiology of the CSF and Blood-Brain Barriers. CRC Press. Boca Raton.
5. Lowery, L.A. & H. Sive. 2004. Strategies of vertebrate neurulation and a re-evaluation of teleost neural tube formation. Mech. Dev. 121: 1189-1197.
6. Lowery, L.A. & H. Sive. 2005. Initial formation of zebrafish brain ventricles occurs independently of circulation and requires the nagie oko and snakehead/Atp1α1a.1 gene products. Development 132: 2057-2067.
7. Götz, M. & W.B. Huttner. 2005. The cell biology of neurogenesis. Nat. Rev. Mol. Cell Biol. 6: 777-788.
8. Lowery, L.A. & H. Sive. 2009. Totally tubular: the mystery behind function and origin of the brain ventricular system. Bioessays. 31: 446-458.
9. Ek, C.J., K.M. Dziegielewska, M.D. Habgood & N.R. Saunders. 2011. Barriers in the developing brain and Neurotoxicology. Neurotoxicology. [Epub ahead of print].
10. Zhang, J., J. Piontek, H. Wolburg, et al. 2010. Establishment of a neuroepithelial barrier by Claudin-5a is essential for zebrafish brain ventricular lumen expansion. Proc. Natl. Acad. Sci. USA 107: 1425-1430.
11. Abdelilah-Seyfried, S. 2010. Claudin-5a in developing zebrafish brain barriers: another brick in the wall. Bioessays 32: 768-776.
12. Furuse, M., M. Hata, K. Furuse, et al. 2002. Claudin-based tight junctions are crucial for the mammalian epidermal barrier: a lesson from claudin-1-deficient mice. J. Cell Biol. 156: 1099-1111.
13. Nitta, T., M. Hata, S. Gotoh, et al. 2003. Size-selective loosening of the blood-brain barrier in Claudin-5-deficient mice. J. Cell Biol. 161: 653-660.
14. Furuse, M. 2009. Knockout animals and natural mutations as experimental and diagnostic tool for studying tight junction functions in vivo. Biochim. Biophys. Acta. 1788: 813-819.
15. Gupta, I.R. & A.K. Ryan. 2010. Claudins: unlocking the code to tight junction function during embryogenesis and in disease. Clin. Genet. 77: 314-325.
16. Morita, K., H. Sasaki, M. Furuse & S. Tsukita. 1999. Endothelial claudin: claudin-5/TMVCF constitutes tight junction strands in endothelial cells. J. Cell Biol. 147: 185-194.
17. Wolburg, H., K. Wolburg-Buchholz, J. Kraus, et al. 2003. Localization of Claudin-3 in tight junctions of the blood-brain barrier is selectively lost during experimental autoimmune encephalomyelitis and human glioblastoma multiforme. Acta Neuropathol. (Berl.) 105: 586-592.
18. Ohtsuki, S., H. Yamaguchi, Y. Katsukura, et al. 2008. mRNA expression levels of tight junction protein genes in mouse brain capillary endothelial cells highly purified by magnetic cell sorting. J. Neurochem. 104: 147-154.
19. Jeong, J.Y., H.B. Kwon, J.C. Ahn, et al. 2008. Functional and developmental analysis of the blood-brain barrier in zebrafish. Brain Res. Bull. 75: 619-628.
20. Xie, J., E. Farage, M. Sugimoto & B. Anand-Apte. 2010. A novel transgenic zebrafish model for blood-brain and blood-retinal barrier development. BMC Dev. Biol. 10: 76.
21. Hyoung Kim, J., Y. Suk Yu, K.W. Kim & J. Hun Kim. 2011. Investigation of barrier characteristics in the hyaloid-retinal vessel of zebrafish. J. Neurosci. Res. 89: 921-928.
22. Loh, Y.H., A. Christoffels, S. Brenner, et al. 2004. Extensive expansion of the claudin gene family in the teleost fish, Fugu rubripes. Genome Res. 7: 1248-1257.
23. Tine, M., H. Kuhl, A. Beck, L. Bargelloni & R. Reinhardt. 2011. Comparative analysis of intronless genes in teleost fish genomes: Insights into their evolution and molecular function. Mar. Genomics. 4: 109-119.
24. Enerson, B.E. & L.R. Drewes. 2006. The rat blood-brain barrier transcriptome. J. Cereb. Blood Flow Metab. 26: 959-973.
25. Wessells, H., C.J. Sullivan, Y. Tsubota, et al. 2009. Transcriptional profiling of human cavernosal endothelial cells reveals distinctive cell adhesion phenotype and role for claudin 11 in vascular barrier function. Physiol. Genomics. 39: 100-108.
26. Piontek, J., L. Winkler, H. Wolburg, et al. 2008. Formation of tight junction: determinants of homophilic interaction between classic claudins. FASEB J. 22: 146-158.
27. Fujita, K., J. Katahira, Y. Horiguchi, et al. 2000. Clostridium perfringens enterotoxin binds to the second extracellular loop of Claudin-3, a tight junction integral membrane protein. FEBS Lett. 476: 258-261.
28. Clelland, E.S. & S.P. Kelly. 2010. Tight junction proteins in zebrafish ovarian follicles: stage specific mRNA abundance and response to 17beta-estradiol, human chorionic gonadotropin, and maturation inducing hormone. Gen. Comp. Endocrinol. 168: 388-400.
29. Schier, A.F., S.C. Neuhauss, M. Harvey, et al. 1996. Mutations affecting the development of the embryonic zebrafish brain. Development 123: 165-178.
30. Sehnert, A.J., A. Huq, B.M. Weinstein, et al. 2002. Cardiac troponin T is essential in sarcomere assembly and cardiac contractility. Nat. Genet. 31: 106-110.