Insulin-like growth factor binding protein-2 as a regulator of IGF actions in CNS: Implications in multiple sclerosis

Daniel Chesik*, Jacques De Keyser, Nadine Wilczak

*Corresponding author for this work

    Research output: Contribution to journalReview articlepeer-review

    44 Citations (Scopus)

    Abstract

    Insulin-like growth factors (IGFs) are indispensable peptide hormones for proper development of the central nervous system (CNS). Because IGF-1 exhibits neuroprotective and myelinogenetic effects, it possesses therapeutic potential in treating neurodegenerative demyelinating diseases such as multiple sclerosis (MS). However, IGF actions are largely dependant on high-affinity regulatory IGF binding proteins (IGFBPs), which are likely to interfere with therapeutic attempts at elevating IGF-1 levels in the CNS. In particular, IGFBP-2 plays a dominant role in IGF regulation in the CNS and is upregulated in several pathological conditions, including MS. The question remains as to whether IGFBPs should be considered "interfering" components of IGF treatment strategies or might possibly be utilized to clinical advantage. This review discusses our current understanding of biological functions of IGFBP-2 in the CNS and its implications in the demyelinating disease MS. (c) 2007 Elsevier Ltd. All rights reserved.

    Original languageEnglish
    Pages (from-to)267-278
    Number of pages12
    JournalCytokine & growth factor reviews
    Volume18
    Issue number3-4
    DOIs
    Publication statusPublished - 2007

    Keywords

    • insulin-like growth factor
    • insulin-like growth factor binding protein-2
    • multiple sclerosis
    • central nervous system
    • demyelination
    • CENTRAL-NERVOUS-SYSTEM
    • EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS
    • FACTOR-I
    • RAT-BRAIN
    • GENE-EXPRESSION
    • CEREBROSPINAL-FLUID
    • EXTRACELLULAR-MATRIX
    • TRANSGENIC MICE
    • CELL-GROWTH
    • TARGETED DISRUPTION

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