Loss of SHP-1 phosphatase alters cytokine expression in the mouse hindbrain following cochlear ablation.

Loss of SHP-1 phosphatase alters cytokine expression in the mouse hindbrain following cochlear ablation.
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耳蜗消融后,SHP-1 磷酸酶的丧失会改变小鼠后脑中细胞因子的表达。

DOI:
10.1016/j.cyto.2004.05.004
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发表时间:
2004
期刊:
Cytokine.
影响因子:
--
通讯作者:
Lurie,DianaI
Lurie,DianaI
中科院分区:
--
文献类型:
--
作者:
Zhao,Jie;Lurie,DianaI

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Inflammatory cytokines in the central nervous system are largely modulated by glial cells and influence neuronal responses to CNS injury. The protein tyrosine phosphatase SHP-1, an intracellular regulator of many cytokine signaling pathways, has been implicated in mediating the activation of glia. There is a direct correlation between abnormally activated microglia and neuron loss within the SHP-1 deficient motheaten (me/me) mouse auditory brainstem after afferent injury. In order to determine whether loss of SHP-1 creates an aberrant cytokine environment driving the abnormal activation of me/me microglia, the expression of interleukin-4 (IL-4), interleukin-10 (IL-10), interleukin-1beta (IL-1β), tumor necrosis factor-alpha (TNF-α), and interferon-gamma (IFN-γ) was examined by enzyme-linked immunosorbent assay (ELISA). Normal uninjured me/me mice showed lower IL-10 but higher IL-1β levels compared to wild-type. Following unilateral cochlear ablation, there is decreased expression of IL-4 and IL-10 in me/me brains compared to wild-type, but IL-1β is significantly increased. These findings indicate that decreases in anti-inflammatory cytokines, in combination with increased expression of the pro-inflammatory cytokine IL-1β, may initiate a robust inflammatory reaction within the me/me brain contributing to the neuronal degeneration in the deafferented me/me auditory brainstem. SHP-1 may therefore play a role in limiting CNS inflammation following injury and disease.
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