CNTFR alpha alone or in combination with CNTF promotes macrophage chemotaxis in vitro.

Abstract:

:Microchemotaxis chambers were used to investigate whether one aspect of ciliary neurotrophic factor CNTF's role as a lesion factor might be to promote the initial early recruitment of macrophages, which express the signal transducing receptor components, gp130 and LIFRbeta. CNTFRalpha alone, or in combination with CNTF, elicited concentration-dependent macrophage chemotaxis that was inhibited by a neutralizing gp 130 antibody. IL-6, but not LIF, similarly promoted gp 130-dependent macrophage chemotaxis. Stimulation of macrophages with either CNTFRalpha in combination with CNTF or IL-6 alone resulted in tyrosine phosphorylation of an approximately 130 kD protein, presumed to be gp130. Macrophage chemotaxis induced by the combination of CNTFRalpha and CNTF was inhibited in a dose-dependent fashion by wortmannin, LY294002 or PD98059, suggesting the involvement of the phosphoinositide-3 kinase and mitogen-activated protein kinase signaling proteins. As CNTFRalpha and CNTF are present, or have immediate access to nerves after injury, these data point to the possibility that this soluble receptor alone or in combination with its ligand may promote the initial early recruitment of macrophages in vivo.

journal_name

Neuropeptides

journal_title

Neuropeptides

authors

Kobayashi H,Mizisin AP

doi

10.1054/npep.2000.0829

keywords:

subject

Has Abstract

pub_date

2000-12-01 00:00:00

pages

338-47

issue

6

eissn

0143-4179

issn

1532-2785

pii

S0143-4179(00)90829-1

journal_volume

34

pub_type

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