|Guchhait, Prasenjit - BAYLOR COLLEGE MED|
|Tosi, Michael - BAYLOR COLLEGE MED|
|Smith, C Wayne|
|Chakraborty, Arup - BAYLOR COLLEGE MED|
Submitted to: Journal of Immunological Methods
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: September 8, 2003
Publication Date: December 1, 2003
Citation: GUCHHAIT, P., TOSI, M.F., SMITH, C.W., CHAKRABORTY, A. 2003. THE MURINE MYELOID CELL LINE 32DC13 AS A MODEL SYSTEM FOR STUDYING NEUTROPHIL FUNCTIONS. JOURNAL OF IMMUNOLOGICAL METHODS. 283:195-204. Interpretive Summary: Studies of innate immunity will benefit from tissue culture models that allow the investigation of critical cell functions. In this paper we present our work in developing a cell line that can be stimulated to become very much like normal neutophils (the most common form of white blood cells). It is our hope that these studies will provide a model for important studies that will enhance our understanding of inflammatory diseases. In fact, we have received numerous requests for these cells and have provided them to other laboratories for study.
Technical Abstract: The murine myeloid cell line 32Dcl3 is one of the few cell lines that can terminally differentiate into neutrophils. Granulocyte colony-stimulating factor (G-CSF) drives the differentiation of these cells; therefore, G-CSF receptor signaling for neutrophil proliferation and differentiation has been studied extensively using this cell line as a model. Differentiated 32Dcl3 cells exhibit a striking morphologic similarity to normal neutrophils; however, the degree to which differentiated 32Dcl3 cells are functionally similar to normal neutrophils remains unknown. In this study, we compared the function of differentiated 32Dcl3 cells with mouse neutrophils. Our results demonstrate that a subclone of differentiated 32Dcl3 cells (32Dcl3C) exhibits normal neutrophil functions of phagocytosis, degranulation, adhesion and shape change in response to appropriate stimuli. These observations suggest that this cell line can serve as an effective model system to study similar mature neutrophil functions. However, 32Dcl3C cells fail to produce superoxide in response proper stimuli.