Previous investigations suggest that the expression of K+ channels in cultured rat microglia is related to the activation status of these cells. Both, lipopolysaccharide (LPS) and agents that raise intracellular cyclic AMP have been shown to inhibit microglial proliferation. LPS also regulates the m
Expression of Kv1.5 K+ channels in activated microglia in vivo
β Scribed by Ilo Jou; Hankyoung Pyo; Sungkwon Chung; So Young Jung; Byoung Joo Gwag; Eun-Hye Joe
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 204 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
β¦ Synopsis
We examined the expression of outward rectifier K Ο© channels in activated microglia in vivo. For this purpose, lipopolysaccharide (LPS, 2 Β΅g) was injected into the cortex near the hippocampal region of rat brains, and K Ο© channel expression was examined using antibodies against shaker-type K Ο© channels, Kv1.5 and Kv1.3. OX-42positive microglia were found around the injection sites from 8 h after the LPS injection and remained there for 3 days. The OX-42-positive microglia expressed Kv1.5 immunoreactivity, and the time course of Kv1.5 expression was closely correlated with that of OX-42. In saline-injected brains, OX-42-positive cells also expressed Kv1.5 immunoreactivity even though far fewer OX-42-positive cells were found. Increase of Kv1.5 expression after LPS injection was also demonstrated by immunoblot analysis. On the other hand, Kv1.3 immunoreactivity was barely detected in OX-42-positive cells over the entire experimental period. The expression of Kv1.5 preceded that of inducible nitric oxide synthase (iNOS), which is a prominent indication of microglial activation. iNOS was not detectable until 12 h, and thereafter it was maintained for 3 days together with Kv1.5 and OX-42. These results suggest that in vivo as well as in vitro activated microglia expressed outward K Ο© channels and that some of the channels at least are Kv1.5.
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