Open Access

High-mobility group box 1 released from astrocytes promotes the proliferation of cultured neural stem/progenitor cells

  • Authors:
    • Man Li
    • Lin Sun
    • Yong Luo
    • Chenchen Xie
    • Yueshan Pang
    • Yuan Li
  • View Affiliations

  • Published online on: June 24, 2014     https://doi.org/10.3892/ijmm.2014.1820
  • Pages: 705-714
  • Copyright: © Li et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY_NC 3.0].

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Abstract

Astrocytes are major components of the adult neurogenic niche and play a crucial role in regulating neural stem cell proliferation and differentiation. Following brain injury, astrocytes become reactive and release high-mobility group box 1 (HMGB1), which plays a crucial role in the inflammatory process. However, although it has been reported that HMGB1 promotes neural stem/progenitor cell (NS/PC) proliferation in the developing brain, whether HMGB1 released by reactive astrocytes regulates NS/PC proliferation remains unknown. In this study, we aimed to investigate whether HMGB1 released from reactive astrocytes enhances NS/PC proliferation and to elucidate the possible mechanisms involved in this process. To evaluate the effects of HMGB1 on NS/PC proliferation, NS/PCs were cultured in HMGB1 culture medium and astrocyte-conditioned medium with or without reactive astrocyte-derived HMGB1 by RNA interference (RNAi). To explore the possible mechanisms, the HMGB1 receptor for advanced glycation endproducts (RAGE) in the NS/PCs was blocked with anti-RAGE antibody, and c-Jun N-terminal protein kinase (JNK) in the NS/PCs was inhibited using the potent JNK inhibitor, SP600125. Our results suggested that HMGB1 released from reactive astrocytes promoted NS/PC proliferation in vitro, and the blockade of RAGE or the inhibition of the JNK signaling pathway in the NS/PCs prevented the HMGB1-induced NS/PC proliferation. Our findings demonstrated that HMGB1 released by reactive astrocytes promoted NS/PC proliferation by binding RAGE and enhancing the phosphorylation of the JNK signaling pathway. These findings support a previously described mechanism of a crosstalk between astrocytes and NS/PCs, and suggest that reactive astrocyte-derived HMGB1 plays an important role in the repair of the central nervous system following brain injury.
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September-2014
Volume 34 Issue 3

Print ISSN: 1107-3756
Online ISSN:1791-244X

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Copy and paste a formatted citation
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Spandidos Publications style
Li M, Sun L, Luo Y, Xie C, Pang Y and Li Y: High-mobility group box 1 released from astrocytes promotes the proliferation of cultured neural stem/progenitor cells. Int J Mol Med 34: 705-714, 2014
APA
Li, M., Sun, L., Luo, Y., Xie, C., Pang, Y., & Li, Y. (2014). High-mobility group box 1 released from astrocytes promotes the proliferation of cultured neural stem/progenitor cells. International Journal of Molecular Medicine, 34, 705-714. https://doi.org/10.3892/ijmm.2014.1820
MLA
Li, M., Sun, L., Luo, Y., Xie, C., Pang, Y., Li, Y."High-mobility group box 1 released from astrocytes promotes the proliferation of cultured neural stem/progenitor cells". International Journal of Molecular Medicine 34.3 (2014): 705-714.
Chicago
Li, M., Sun, L., Luo, Y., Xie, C., Pang, Y., Li, Y."High-mobility group box 1 released from astrocytes promotes the proliferation of cultured neural stem/progenitor cells". International Journal of Molecular Medicine 34, no. 3 (2014): 705-714. https://doi.org/10.3892/ijmm.2014.1820