Placenta
Volume 30, Issue 10 , Pages 848-854 , October 2009

The Presence of Kinesin Superfamily Motor Proteins KIFC1 and KIF17 in Normal and Pathological Human Placenta

,Accepted 16 July 2009.

References 

  1. Benirschke K, Kaufmann P. Pathology of the human placenta. New York, Berlin: Springer-Verlag; 2000;
  2. King BF. Comparative anatomy of the placental barrier. Bibl Anat. 1982;22:13–28
  3. Baumann MU, Deborde S, Illsley NP. Placental glucose transfer and fetal growth. Endocrine. 2002;19:13–22
  4. Young AM, Allen CE, Audus KL. Efflux transporters of the human placenta. Adv Drug Deliv Rev. 2003;55:125–132
  5. Vallee RB, Williams JC, Varma D, Barnhart LE. Dynein: an ancient motor protein involved in multiple modes of transport. J Neurobiol. 2004;58:189–200
  6. Hirokawa N. Kinesin and dynein superfamily proteins and the mechanism of organelle transport. Science. 1998;279:519–526
  7. Hirokawa N, Takemura R. Kinesin superfamily proteins. In:  Schliwa M editors. Molecular motors. Weinheim: Wiley-VCH; 2003;p. 79–109
  8. Sharp DJ, Rogers GC, Scholey JM. Microtubule motors in mitosis. Nature. 2000;407:41–47
  9. Miki H, Setou M, Kaneshiro K, Hirokawa N. All kinesin superfamily protein, KIF, genes in mouse and human. Proc Natl Acad Sci USA. 2001;98:7004–7011
  10. Vale RD. The molecular motor toolbox for intracellular transport. Cell. 2003;112:467–480
  11. Kayadjanian N, Lee HS, Pina-Crespo J, Heinemann SF. Localization of glutamate receptors to distal dendrites depends on subunit composition and the kinesin motor protein KIF17. Mol Cell Neurosci. 2007;34:219–230
  12. Kamal A, Goldstein LS. Principles of cargo attachment to cytoplasmic motor proteins. Curr Opin Cell Biol. 2002;14:63–68
  13. Nakagawa T, Setou M, Seog D, Ogasawara K, Dohmae N, Takio K, et al. A novel motor, KIF13A, transports mannose-6-phosphate receptor to plasma membrane through direct interaction with AP-1 complex. Cell. 2000;103:569–581
  14. Setou M, Nakagawa T, Seog DH, Hirokawa N. Kinesin superfamily motor protein KIF17 and mLin-10 in NMDA receptor-containing vesicle transport. Science. 2000;288:1796–1802
  15. Novak D, Lehman M, Bernstein H, Beveridge M, Cramer S. SNAT expression in rat placenta. Placenta. 2006;27:510–516
  16. Yamaguchi M, Sakata M, Ogura K, Miyake A. Gestational changes of glucose transporter gene expression in the mouse placenta and decidua. J Endocrinol Invest. 1996;19:567–569
  17. Mathias AA, Hitti J, Unadkat JD. P-glycoprotein and breast cancer resistance protein expression in human placentae of various gestational ages. Am J Physiol Regul Integr Comp Physiol. 2005;289:R963–R969
  18. Navolanic PM, Sperry AO. Identification of isoforms of a mitotic motor in mammalian spermatogenesis. Biol Reprod. 2000;62:1360–1369
  19. Noda Y, Sato-Yoshitake R, Kondo S, Nangaku M, Hirokawa N. KIF2 is a new microtubule-based anterograde motor that transports membranous organelles distinct from those carried by kinesin heavy chain or KIF3A/B. J Cell Biol. 1995;129:157–167
  20. Lawrence CJ, Dawe RK, Christie KR, Cleveland DW, Dawson SC, Endow SA, et al. A standardized kinesin nomenclature. J Cell Biol. 2004;167:19–22
  21. Yang WX, Sperry AO. C-terminal kinesin motor KIFC1 participates in acrosome biogenesis and vesicle transport. Biol Reprod. 2003;69:1719–1729
  22. Nath S, Bananis E, Sarkar S, Stockert RJ, Sperry AO, Murray JW, et al. Kif5B and Kifc1 interact and are required for motility and fission of early endocytic vesicles in mouse liver. Mol Biol Cell. 2007;18:1839–1849
  23. Yang WX, Jefferson H, Sperry AO. The molecular motor KIFC1 associates with a complex containing nucleoporin NUP62 that is regulated during development and by the small GTPase RAN. Biol Reprod. 2006;74:684–690
  24. Zhang Y, Sperry AO. Comparative analysis of two C-terminal kinesin motor proteins: KIFC1 and KIFC5A. Cell Motil Cytoskeleton. 2004;58:213–230
  25. Leach L, Firth JA. Fine structure of the paracellular junctions of terminal villous capillaries in the perfused human placenta. Cell Tissue Res. 1992;268:447–452
  26. Miki H, Okada Y, Hirokawa N. Analysis of the kinesin superfamily: insights into structure and function. Trends Cell Biol. 2005;15:467–476
  27. Seval Y, Korgun ET, Demir R. Hofbauer cells in early human placenta: possible implications in vasculogenesis and angiogenesis. Placenta. 2007;28:841–845
  28. Demir R, Seval Y, Huppertz B. Vasculogenesis and angiogenesis in the early human placenta. Acta Histochem. 2007;109:257–265
  29. Macho B, Brancorsini S, Fimia GM, Setou M, Hirokawa N, Sassone-Corsi P. CREM-dependent transcription in male germ cells controlled by a kinesin. Science. 2002;298:2388–2390
  30. Hogeveen KN, Sassone-Corsi P. Regulation of gene expression in post-meiotic male germ cells: CREM-signalling pathways and male fertility. Hum Fertil. 2006;9:73–79
  31. Kotaja N, Lin H, Parvinen M, Sassone-Corsi P. Interplay of PIWI/argonaute protein MIWI and kinesin KIF17b in chromatoid bodies of male germ cells. J Cell Sci. 2006;119:2819–2825
  32. Kimmins S, Kotaja N, Fienga G, Kolthur US, Brancorsini S, Hogeveen K, et al. A specific programme of gene transcription in male germ cells. Reprod Biomed Online. 2004;8:496–500
  33. Saade M, Irla M, Govin J, Victorero G, Samson M, Nguyen C. Dynamic distribution of Spatial during mouse spermatogenesis and its interaction with the kinesin KIF17b. Exp Cell Res. 2007;313:614–626
  34. Kotaja N, De Cesare D, Macho B, Monaco L, Brancorsini S, Goossens E, et al. Abnormal sperm in mice with targeted deletion of the act (activator of cAMP-responsive element modulator in testis) gene. Proc Natl Acad Sci USA. 2004;101:10620–10625
  35. Hoeffler JP, Meyer TE, Yun Y, Jameson JL, Habener JF. Cyclic AMP-responsive DNA-binding protein: structure based on a cloned placental cDNA. Science. 1988;242:1430–1433
  36. Foulkes NS, Borrelli E, Sassone-Corsi P. CREM gene: use of alternative DNA-binding domains generates multiple antagonists of cAMP-induced transcription. Cell. 1991;64:739–749
  37. Heckert LL, Schultz K, Nilson JH. The cAMP response elements of the alpha subunit gene bind similar proteins in trophoblasts and gonadotropes but have distinct functional sequence requirements. J Biol Chem. 1996;271:31650–31656
  38. Bell GI, Kayano T, Buse JB, Burant CF, Takeda J, Lin D, et al. Molecular biology of mammalian glucose transporters. Diabetes Care. 1990;13:198–208
  39. Hahn T, Desoye G. Ontogeny of glucose transport systems in the placenta and its progenitor tissues. Early Pregnancy. 1996;2:168–182
  40. Bunn RC, Jensen MA, Reed BC. Protein interactions with the glucose transporter binding protein GLUT1CBP that provides a link between GLUT1 and the cytoskeleton. Mol Biol Cell. 1999;10:819–832

PII: S0143-4004(09)00236-7

doi: 10.1016/j.placenta.2009.07.005

Placenta
Volume 30, Issue 10 , Pages 848-854 , October 2009

Article Tools

* Image Usage & Resolution