Chemistry: molecular biology and microbiology – Animal cell – per se ; composition thereof; process of...
Patent
1998-06-10
2000-10-03
Mertz, Prema
Chemistry: molecular biology and microbiology
Animal cell, per se ; composition thereof; process of...
435366, 435369, 4352523, C12N 510, C12N 516, C12N 522
Patent
active
061271764
ABSTRACT:
Mutant cell lines which have lost their ability to respond to IL-1 are provided. In one embodiment, the mutant cell line lacks or is essentially free of IL-1 receptor associate kinase (IRAK), an IL-1 signaling pathway component. The present invention also provides a method for making mutant cell lines that are unresponsive to IL-1, TNF, or to both cytokines. The method comprises the steps of: transfecting cells with a Herpes Simplex Virus thymidine kinase (HSV-TK) gene and a second gene for positive selection, each of said genes being operatively linked to an IL-1 inducible promoter or a TNF inducible promoter; selecting for transfected cells that express HSV thymidine kinase and the product of the positive selection gene in response to IL-1 or TNF; determining a gancyclovir concentration which kills the selected cells in the presence of IL-1 or TNF and which does not kill the selected cells in the absence of IL-1 or TNF; mutagenizing the selected cells using a chemical mutagenizing agent; and treating the mutagenized cells with the determined concentration of gancyclovir and IL-1 or TNF. The present invention also relates to a method of identifying domains or amino acids in IRAK that are essential for IRAK to function in the IL-1 signaling pathway.
REFERENCES:
Altmeyer et al. Cellular Immunology, vol. 138(1), pp. 94-107, Oct. 1991.
"Jak-STAT Pathways and Transcriptional Activation in Response to IFNs and Other Extracellular Signaling Proteins" by Darnell, et al., Scientce, vol. 264, Jun. 3, 1994, pp. 1415-1421.
"Use of a Selectable Marker Regulated by Alpha Interferon To Obtain Mutations in the Signaling Pathway" by Pelligrini, et al., Molecular and Cellular Biology, vol. 9, No. 11, Nov. 1989, pp. 4605-4612.
"RIP mediates tumor necrosis factor receptor 1 activation of NF-.kappa.B but not Fas/APO-1 initiated apoptosis" by Ting, et al., The EMBO Journal, vol. 15, No. 22, 1996, pp. 6189-6196.
"Early Lethality, Functional NF-.kappa.B Activation, and Increased Sensitivity to TNF-Inducesd Cell Death in TRAF2-Deficient Mice" by Yeh, et al., Immunity, vol. 7, Nov. 1997, pp. 715-725.
MyD88: An Adapter That Recruits IRAK to the IL-1 Receptor Complex by Wesche, et al., Immunity, vol. 7, Dec. 1997, pp. 837-847.
"A cytokine-responsive I.kappa.B kinase that activates the transcription factor NF-.kappa.B" by DiDonato, et al., Nature, vol. 388/7, Aug. 1997, pp. 548-554.
"Identification and Characterization of an I.kappa.B Kinase" by Regnier, et al., Cell, vol. 90, Jul. 25, 1997, pp. 373-383.
"Complementation Cloning of NEMO, a Component of the I.kappa.B Kinase Complex Essential for NF-.kappa.B Activation" by Yamaoka, et al., Cell, vol. 93, Jun. 26, 1998, pp. 1231-1240.
"IRAK: A Kinase Associated with the Interleukin-1 Receptor" by Cao, et al., Science, vol. 271, Feb. 23, 1996, pp. 1128-1131.
Li Xiaoxia
Stark George R.
Cleveland Clinic Foundation
Hamud Fozia
Mertz Prema
LandOfFree
Mutant cell lines unresponsive to interleukin 1 does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Mutant cell lines unresponsive to interleukin 1, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Mutant cell lines unresponsive to interleukin 1 will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-194306