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Nogo receptor-mediated blockade of axonal growth

a nogo receptor and axonal growth technology, applied in the field of neuronal and molecular biology, can solve the problems of damage to the axon, the degradation of the myelin surrounding the axon, and the inability of the damaged neurons to regenerate in the central, and achieve the effect of high stringency conditions

Inactive Publication Date: 2008-09-11
YALE UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

When an elongation comes in contact with a surface that is unfavorable, it withdraws.
Damaged neurons do not regenerate in the central nervous system (CNS) following injury due to trauma and disease.
Both developing and mature forms of myelin are susceptible to injury from disease or physical trauma resulting in degradation of the myelin surrounding axons.

Method used

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  • Nogo receptor-mediated blockade of axonal growth
  • Nogo receptor-mediated blockade of axonal growth
  • Nogo receptor-mediated blockade of axonal growth

Examples

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Effect test

example 1

Identification of Nogo as a Member of the Reticulon Family of Proteins

[0220]Adult mammalian axon regeneration is generally successful in the periphery but dismally poor in the CNS. However, many classes of CNS axons can extend for long distances in peripheral nerve grafts (Benfy & Aguayo (1982) Nature 296, 150-152). Comparison of CNS and peripheral nervous system (PNS) myelin has revealed that CNS white matter is selectively inhibitory for axonal outgrowth (Schwab & Thoenen (1985) J. Neurosci. 5, 2415-2423). Several components of CNS white matter, NI35, NI250 (Nogo) and MAG, with inhibitory activity for axon extension have been described (Wang et al., (1999) Transduction of inhibitory signals by the axonal growth cone, in Neurobiology of Spinal Cord Injury, Kalb & Strittmatter (editors) Humana Press; Caroni & Schwab, (1988) J. Cell Biol. 106, 1281-1288; Spillmann et al., (1998) J. Biol. Chem. 73, 19283-19293; McKerracher et al., (1994) Neuron 13, 805-811; Mukhopadhyay et al., (1994)...

example 2

Polyclonal Antibodies against Nogo

[0227]The predicted intra-membrane topology of the two hydrophobic domains of Nogo indicates that the 66 amino acid residues between these segments is localized to the lumenal / extracellular face of the membrane. To explore this further, an antiserum directed against the 66 amino acid domain was generated.

[0228]For antibody production and immunohistology, anti-Myc immunoblots and immunohistology with the 9E10 antibody were obtained as described in Takahashi et al., (1998) Nature Neurosci., 1, 487-493 & Takahashi et al., (1999) Cell, 99, 59-69. The GST-Nogo fusion protein was employed as an immunogen to generate an anti-Nogo rabbit antiserum. Antibody was affinity-purified and utilized at 3 μg / ml for immunohistology and 1 μg / ml for immunoblots. To assess the specificity of the antiserum, staining was conducted in the presence of GST-Nogo protein at 0.1 mg / ml. For live cell staining, cells were incubated in primary antibody dilutions at 4° C. for one h...

example 3

Nogo Expression in the Central Nervous System

[0230]If Nogo is a major contributor to the axon outgrowth inhibitory characteristics of CNS myelin as compared to PNS myelin (Caroni & Schwab, (1988) J. Cell Biol. 106, 1281-1288; Spillmann et al., (1998) J. Biol. Chem. 73, 19283-19293; Bregman et al., (1995) Nature 378, 498-501), then Nogo should be expressed in adult CNS myelin but not PNS myelin. Northern blot analysis of Nogo expression was performed using probes derived from the 5′ Nogo-A / B-specific region and from the 3′ Nogo common region of the cDNA. A single band of about 4.1 kilobase was detected with the 5′ probe in adult rat optic nerve total RNA samples, but not sciatic nerve samples. The results indicate that the Nogo-A clone is a full length cDNA, and are consistent with a role for Nogo as a CNS-myelin-specific axon outgrowth inhibitor. Northern blot analysis with a 3′ probe reveals that optic nerve expresses high levels of the Nogo-A mRNA and much lower levels of Nogo-B a...

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Abstract

Disclosed are NgR proteins and biologically active Nogo (ligand) protein fragments. Also disclosed are compositions and methods for modulating the expression or activity of the Nogo and NgR protein. Also disclosed are peptides which block Nogo-mediated inhibition of axonal extension. The compositions and methods of the invention are useful in the treatment of cranial or cerebral trauma, spinal cord injury, stroke or a demyelinating disease.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a divisional of U.S. application Ser. No. 09 / 972,599, filed Oct. 6, 2001, which is a continuation-in-part of U.S. application Ser. No. 09 / 758,140, filed Jan. 12, 2001, which claims benefit under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 60 / 175,707 filed Jan. 12, 2000; U.S. Provisional Application No. 60 / 207,366 filed May 26, 2000; and U.S. Provisional Application No. 60 / 236,378 filed Sep. 29, 2000 which are herein incorporated by reference in their entireties. U.S. application Ser. No. 09 / 972,599 is also a continuation-in-part of international application PCT / US01 / 01041, filed Jan. 12, 2001.U.S. GOVERNMENT SUPPORT[0002]This invention was partially made with government support under National Institute of Health Grant RO1-NS 33020, RO1-NS39962 and RO1-NS42304.FIELD OF THE INVENTION[0003]The invention relates to neurology and molecular biology. More particularly, the invention relates to CNS neurons and axona...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K39/395C07H21/04C12N15/64C12N5/08G01N33/53C12P21/00C07K16/18A61K38/16G01N33/50A61K38/00A61K38/17A61K45/06A61P25/00A61P25/02A61P25/04A61P25/06A61P25/14A61P25/28A61P43/00C07K14/705C07K16/28C12N1/15C12N1/19C12N1/21C12N5/10C12N15/09C12P21/02C12Q1/02G01N33/15
CPCA01K2217/05A61K38/00A61K2039/505C07K14/705C07K16/18C07K16/28C07K2319/00G01N33/50C07K14/47C07K14/70571A61P25/00A61P25/02A61P25/04A61P25/06A61P25/14A61P25/28A61P29/00A61P37/00A61P43/00A61P9/00C07K16/286C07K2317/76
Inventor STRITTMATTER, STEPHEN M.
Owner YALE UNIV
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