An activated protein C analog stimulates neuronal production by human neural progenitor cells via a PAR1-PAR3-S1PR1-Akt pathway

Huang Guo, Zhen Zhao, Qi Yang, Min Wang, Robert D. Bell, Su Wang, Nienwen Chow, Thomas P Davis, John H. Griffin, Steven A. Goldman, Berislav V. Zlokovic

Research output: Contribution to journalArticle

37 Citations (Scopus)

Abstract

Activated protein C (APC) is a protease with anticoagulant and cell-signaling activities. In the CNS, APC and its analogs with reduced anticoagulant activity but preserved cell signaling activities, such as 3K3A-APC, exert neuroprotective, vasculoprotective, and anti-inflammatory effects. Murine APC promotes subependymal neurogenesis in rodents in vivo after ischemic and traumatic brain injury. Whether human APC can influence neuronal production from resident progenitor cells in humans is unknown. Here we show that 3K3A-APC, but not S360A-APC (an enzymatically inactive analog of APC), stimulates neuronal mitogenesis and differentiation from fetal human neural stem and progenitor cells (NPCs). The effects of 3K3A-APC on proliferation and differentiation were comparable to those obtained with fibroblast growth factor and brain-derived growth factor, respectively. Its promoting effect on neuronal differentiation was accompanied by inhibition of astroglial differentiation. In addition, 3K3A-APC exerted modest anti-apoptotic effects during neuronal production. These effects appeared to be mediated through specific protease activated receptors (PARs) and sphingosine-1-phosphate receptors (S1PRs), in that siRNA-mediated inhibition of PARs 1-4 and S1PRs 1-5 revealed that PAR1, PAR3, and S1PR1 are required for the neurogenic effects of 3K3A-APC. 3K3A-APC activated Akt, a downstream target of S1PR1, which was inhibited by S1PR1, PAR1, and PAR3 silencing. Adenoviral transduction of NPCs with a kinase-defective Akt mutant abolished the effects of 3K3A-APC on NPCs, confirming a key role of Akt activation in 3K3A-APC-mediated neurogenesis. Therefore, APC and its pharmacological analogs, by influencing PAR and S1PR signals in resident neural progenitor cells, may be potent modulators of both development and repair in the human CNS.

Original languageEnglish (US)
Pages (from-to)6181-6190
Number of pages10
JournalJournal of Neuroscience
Volume33
Issue number14
DOIs
StatePublished - Apr 3 2013

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Protein C
Stem Cells
PAR-1 Receptor
Lysosphingolipid Receptors
Neural Stem Cells
Neurogenesis
Anticoagulants
Fibroblast Growth Factors
Small Interfering RNA
Rodentia
Peptide Hydrolases
Anti-Inflammatory Agents
Phosphotransferases

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

An activated protein C analog stimulates neuronal production by human neural progenitor cells via a PAR1-PAR3-S1PR1-Akt pathway. / Guo, Huang; Zhao, Zhen; Yang, Qi; Wang, Min; Bell, Robert D.; Wang, Su; Chow, Nienwen; Davis, Thomas P; Griffin, John H.; Goldman, Steven A.; Zlokovic, Berislav V.

In: Journal of Neuroscience, Vol. 33, No. 14, 03.04.2013, p. 6181-6190.

Research output: Contribution to journalArticle

Guo, H, Zhao, Z, Yang, Q, Wang, M, Bell, RD, Wang, S, Chow, N, Davis, TP, Griffin, JH, Goldman, SA & Zlokovic, BV 2013, 'An activated protein C analog stimulates neuronal production by human neural progenitor cells via a PAR1-PAR3-S1PR1-Akt pathway', Journal of Neuroscience, vol. 33, no. 14, pp. 6181-6190. https://doi.org/10.1523/JNEUROSCI.4491-12.2013
Guo, Huang ; Zhao, Zhen ; Yang, Qi ; Wang, Min ; Bell, Robert D. ; Wang, Su ; Chow, Nienwen ; Davis, Thomas P ; Griffin, John H. ; Goldman, Steven A. ; Zlokovic, Berislav V. / An activated protein C analog stimulates neuronal production by human neural progenitor cells via a PAR1-PAR3-S1PR1-Akt pathway. In: Journal of Neuroscience. 2013 ; Vol. 33, No. 14. pp. 6181-6190.
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AU - Bell, Robert D.

AU - Wang, Su

AU - Chow, Nienwen

AU - Davis, Thomas P

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