Therapeutic efficacy of sonic hedgehog protein in experimental diabetic neuropathy

被引:80
作者
Calcutt, NA [1 ]
Allendoerfer, KL
Mizisin, AP
Middlemas, A
Freshwater, JD
Burgers, M
Ranciato, R
Delcroix, JD
Taylor, FR
Shapiro, R
Strauch, K
Dudek, H
Engber, TM
Galdes, A
Rubin, LL
Tomlinson, DR
机构
[1] Univ Calif San Diego, Dept Pathol, La Jolla, CA 92093 USA
[2] Curis Inc, Cambridge, MA USA
[3] Univ Manchester, Sch Biol Sci, Div Neurosci, Manchester, Lancs, England
[4] Biogen Inc, Cambridge, MA 02142 USA
关键词
D O I
10.1172/JCI200315792
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hedgehog proteins modulate development and patterning of the embryonic nervous system. As expression of desert hedgehog and the hedgehog receptor, patched-1, persist in the postnatal and adult peripheral nerves, the hedgehog pathway may have a role in maturation and maintenance of the peripheral nervous system in normal and disease states. We measured desert hedgehog expression in the peripheral nerve of maturing diabetic rats and found that diabetes caused a significant reduction in desert hedgehog mRNA. Treating diabetic rats with a sonic hedgehog-IgG fusion protein fully restored motor- and sensory-nerve conduction velocities and maintained the axonal caliber of large myelinated fibers. Diabetes-induced deficits in retrograde transport of nerve growth factor and sciatic-nerve levels of calcitonin gene-related product and neuropeptide Y were also ameliorated by treatment with the sonic hedgehog-IgG fusion protein, as was thermal hypoalgesia in the paw. These studies implicate disruption of normal hedgehog function in the etiology of diabetes-induced peripheral-nerve dysfunction and indicate that delivery of exogenous hedgehog proteins may have therapeutic potential for the treatment of diabetic neuropathy.
引用
收藏
页码:507 / 514
页数:8
相关论文
共 48 条
  • [1] ALLENDOERFER KL, 2001, SOC NEUROSCI
  • [2] [Anonymous], 1979, STEREOLOGICAL METHOD
  • [3] BERG A, 2000, SOC NEUROSCI
  • [4] HEDGEHOG AND BMP GENES ARE COEXPRESSED AT MANY DIVERSE SITES OF CELL-CELL INTERACTION IN THE MOUSE EMBRYO
    BITGOOD, MJ
    MCMAHON, AP
    [J]. DEVELOPMENTAL BIOLOGY, 1995, 172 (01) : 126 - 138
  • [5] ALDOSE REDUCTASE INHIBITION, DOPPLER FLUX AND CONDUCTION IN DIABETIC RAT NERVE
    CALCUTT, NA
    MIZISIN, AP
    KALICHMAN, MW
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1994, 251 (01) : 27 - 33
  • [6] Prosaposin gene expression and the efficacy of a prosaposin-derived peptide in preventing structural and functional disorders of peripheral nerve in diabetic rats
    Calcutt, NA
    Campana, WM
    Eskeland, NL
    Mohiuddin, L
    Dines, KC
    Mizisin, AP
    O'Brien, JS
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1999, 58 (06) : 628 - 636
  • [7] DIFFERENT EFFECTS OF 2 ALDOSE REDUCTASE INHIBITORS ON NOCICEPTION AND PROSTAGLANDIN-E
    CALCUTT, NA
    LI, L
    YAKSH, TL
    MALMBERG, AB
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1995, 285 (02) : 189 - 197
  • [8] REDUCED CILIARY NEURONOTROPHIC FACTOR-LIKE ACTIVITY IN NERVES FROM DIABETIC OR GALACTOSE-FED RATS
    CALCUTT, NA
    MUIR, D
    POWELL, HC
    MIZISIN, AP
    [J]. BRAIN RESEARCH, 1992, 575 (02) : 320 - 324
  • [9] Vascular factors and metabolic interactions in the pathogenesis of diabetic neuropathy
    Cameron, NE
    Eaton, SEM
    Cotter, MA
    Tesfaye, S
    [J]. DIABETOLOGIA, 2001, 44 (11) : 1973 - 1988
  • [10] Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
    Chiang, C
    Ying, LTT
    Lee, E
    Young, KE
    Corden, JL
    Westphal, H
    Beachy, PA
    [J]. NATURE, 1996, 383 (6599) : 407 - 413