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. 2007 Jan 6;3(1-2):39–51. doi: 10.1007/s11302-006-9035-x

Table 2.

Summary of extracellular nucleotide regulation of iNOS expression and NO production by immune cells

LPS-stimulated event and system studied Nucleotide and effect* References
Nitric oxide (NO) production
LPS+ IFNγ-treated murine (CD-1) peritoneal macrophages 2-MeS-ATP: ↑ [83]
LPS-treated RAW 264.7 murine macrophages oATP: ↑ [65, 87]
LPS-treated RAW 264.7 murine macrophages ADP: ↑ [85]
LPS-treated RAW 264.7 murine macrophages ATP: ↑ [86]
LPS-treated RAW 264.7 murine macrophages ATP or BzATP: ↑ [66]
LPS-treated rat astrocytes ATP, ADP, AMP, UTP, BzATP, or 2-MeS-ATP: ↑ [88]
oATP: ↑
IFNγ-treated BV-2 murine microglia cells ATP, ADP, BzATP, or 2-MeS-ATP: ↑ [89]
IL-1β/IFNγ-treated human astrocytes BzATP: ↑ [90]
iNOS expression
LPS-treated RAW 264.7 murine macrophages ATP: ↑ [84]
LPS+ IFNγ-treated murine (CD-1) peritoneal macrophages 2-MeS-ATP: ↑ [83]
LPS-treated RAW 264.7 murine macrophages PPADS: ↑oATP: ↑ [87]
LPS-treated RAW 264.7 murine macrophages BzATP: ↑ [65, 66]
LPS-treated RAW 264.7 murine macrophages ATP: ↑ [88]
IFNγ-treated murine BV-2 microglia cells BzATP or ATP: ↑ [89]

* The upward arrow (↑ indicates that the specified nucleotide enhanced the indicated parameter (NO production or iNOS expression), whereas the downward arrow (↑ designates that the specified nucleotide or inhibitor attenuated the indicated parameter.