Detection of the Activities of Multiple Protein Kinases in Lipopolysaccharide-Stimulated Macrophages by Renaturation.
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- Shinomiya Hiroto
- Department of Immunology and Host Defenses, Ehime University School of Medicine
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- Murakami Osamu
- Department of Immunology and Host Defenses, Ehime University School of Medicine Department of Surgery, Shiga Medical College
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- Nakano Masayasu
- Department of Microbiology, Jichi Medical School
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- Utsumi Sayaka
- Department of Immunology and Host Defenses, Ehime University School of Medicine
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Past studies of individual kinases have demonstrated that protein phosphorylation plays a crucial role in the intracellular signaling pathway of bacterial lipopolysaccharide (LPS). However, no one has determined how many kinases may be activated collectively by LPS stimulation. We examined the spectrum of protein kinases activated in macrophages in response to LPS. Activity was assessed by a renatuiation method that exploited the eability of proteins denatured with sodium dodcyl sulfate and then blotted onto a membrane to regain enzymatic activity after guanidine treatment. Seven electrophoretically-distinct protein kinases with apparent molecular masses of 78, 74, 62, 59, 58, 52, and 48-kDa were detected in lysates from unstimulated murine peritoneal macrophages. An additional three kinases, with apparent molecular masses of 82, 55, and 46-kDa, were detected when the macrophages were stimulated with LPS. The activation of these protein kinases may be dictated by complex signals that are delivered by receptor complexes, including Toll-like receptor 4. These results should provide a clue to clarifying the pleiotropic action of LPS on macrophages.
収録刊行物
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- Journal of Clinical and Experimental Hematopathology
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Journal of Clinical and Experimental Hematopathology 41 (2), 115-118, 2001
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詳細情報 詳細情報について
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- CRID
- 1390001204702595712
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- NII論文ID
- 10010311547
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- NII書誌ID
- AA11556796
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- ISSN
- 18809952
- 13464280
- http://id.crossref.org/issn/13464280
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可