4.2 Article

In vivo validation of signaling pathways regulating human monocyte chemotaxis

Journal

JOURNAL OF IMMUNOLOGICAL METHODS
Volume 330, Issue 1-2, Pages 86-95

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jim.2007.11.011

Keywords

monocytes; transfection; adoptive transfer; chemotaxis; PKC beta

Funding

  1. NCRR NIH HHS [M01 RR 018390, M01 RR018390] Funding Source: Medline
  2. NHLBI NIH HHS [HL 61971, HL 74451, R01 HL051068-08, P01 HL087018-01A10003, R01 HL061971, P01 HL087018, R01 HL074451-04, R01 HL074451] Funding Source: Medline

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Identification of novel signal transduction pathways regulating monocyte chemotaxis can indicate unique targets for preventive therapies for treatment of chronic inflammatory diseases. To aid in this endeavor we report conditions for optimal transfection of primary human monocytes coupled with a new model system for assessing their chemotactic activity in vivo. This method can be used as a tool to identify the relevant signal transduction pathways regulating human monocyte chemotaxis to MCP-1 in the complex in vivo environment that were previously identified to regulate chemotaxis in vitro. MCP-1-dependent chemotaxis of monocytes is studied in an adoptive transfer model where human monocytes transfected with mutant cDNAs are transferred to mice followed by initiation of peritonitis. Harvesting peritoneal cells at 24 h diminishes the contribution of immunologic responses to the cross-species transfer. Validation of relevant regulatory molecules in vivo is critical for understanding the most relevant therapeutic targets for drug development. (C) 2007 Elsevier B.V. All rights reserved.

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