4.7 Article

Luteolin stimulates the NGF-induced neurite outgrowth in cultured PC12 cells through binding with NGF and potentiating its receptor signaling

期刊

FOOD & FUNCTION
卷 12, 期 22, 页码 11515-11525

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1fo01096d

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资金

  1. Key-Area Research and Development Program of Guangdong Province [2020B1111110006]
  2. Special Project of Foshan University of Science and Technology in 2019 [FSUST19-SRI10]
  3. GBA Institute of Collaborate Innovation [GICI-022]
  4. Shenzhen Science and Technology Innovation Committee [ZDSYS201707281432317, JCYJ20170413173747440, JCYJ20180306174903174]
  5. Zhongshan Municipal Bureau of Science and Technology [ZSST20SC03]
  6. Guangzhou Science and Technology Committee Research Grant [GZSTI16SC02, GZSTI17SC02]
  7. Hong Kong RGC Theme-based Research Scheme [T13-605/18-W]
  8. Hong Kong Innovation Technology Fund [UIM/340, UIM/385, ITS/500/18FP, TCPD/17-9]
  9. [TUYF19SC02]
  10. [PD18SC01]
  11. [HMRF18SC06]
  12. [HMRF20SC07]

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The study demonstrated that luteolin can directly interact with nerve growth factor (NGF), enhancing NGF-induced neuronal differentiation and neurofilament expression in cultured PC12 cells. The co-treatment also activated key signaling pathways involved in neuronal growth, mimicking the effects of a high dose of NGF. These findings support the potential development of luteolin as a therapeutic agent for NGF insufficiency-related neurodegenerative diseases.
Luteolin, a flavonoid in fruits and vegetables, has neurotrophic functions without a well-characterized mechanism. Here, we hypothesize a direct interaction of luteolin with nerve growth factor (NGF); as such, the functionality of the NGF could be potentiated. The direct binding of luteolin with NGF was validated by ultra-filtration, Biacore, and docking analyses. In cultured PC12 cells, application of luteolin in combination with a low dose of NGF potentiated the NGF-induced differentiation of neurons by an increase of the differentiated cell number to 25.4 +/- 4.8% (p < 0.01), as well as the increased expression of neurofilaments by 119 +/- 32.1% (p < 0.05), 191 +/- 12.6% (p < 0.01), and 110 +/- 23.4% (p < 0.05) for NF68, NF160 and NF200, respectively. The co-treatment induced the phosphorylations of tropomyosin receptor kinase A (TrkA), extracellular signal-regulated kinase 1/2 (ERK1/2), protein kinase B (Akt), phospholipase C-gamma 1 (PLC gamma 1), and cAMP response element-binding protein (CREB) by 2 to 3 fold: these induced phosphorylations were mimicking that of a high dose of NGF. Moreover, the application of the TrkA inhibitor, K252a, blocked the luteolin-mediated induction of neurofilament expression and neurite outgrowth in cultured PC12 cells, suggesting the target specificity. The result supports the development of luteolin as a therapeutic, or preventive, agent for NGF insufficiency-associated neurodegenerative diseases.

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