Ccr1 Knockout

Constitutive Knock Out

Ccr1 Constitutive Knock Out Mouse Model
The NIAID Exchange Program has closed and live production of this model has ceased. This webpage is retained for historical reference, but this model is not available from Taconic.

  • Model #
  • Genotype
  • Nomenclature
  • 4087-F
    ko/ko
    B6.129S4-Ccr1tm1Gao N10+N5
  • 4087-M
    ko/ko
    B6.129S4-Ccr1tm1Gao N10+N5
Chemokine (C-C motif) receptor 1 (Ccr1) is expressed in neutrophils, monocytes, lymphocytes, eosinophils, and dendritic cells, and binds the leukocyte chemoattractant and hematopoiesis regulator MIP-1alpha, as well as several related CC chemokines. The initial analysis indicated that the Ccr1 Knockout mouse has impaired hematopoiesis, host defense, and inflammatory responses. The knockout mouse also has alterations in the type 1-type 2 cytokine balance.

Genetic Background:

C57BL/6 Background

Origin:

Drs. Ji-Liang Gao and Philip Murphy in the Laboratory of Host Defenses, NIAID, NIH generated the Ccr1 Knockout mouse in 1997. The Ccr1 gene was disrupted by replacing 352 base pair fragment in the middle of the intronless open reading frame with a neomycin resistance gene. The Ccr1 gene was disrupted in 129S4/SvJae-derived J1 ES cells. Resultant chimeras were backcrossed to C57BL/6NAi mice for 10 generations in the NIAID barrier facility at Taconic. At this point, it was discovered that the C57NL/6NAi line had become contaminated with IFNg knockout gene. Line 4087 was then backrossed an additional 5 times to C57BL/6NTac in order to eliminate the contaminating gene and put the strain on the Taconic C57BL/6 subline.


Availability:

This model is no longer available.

Color:

Black

Species:

Mouse

Initial Publication:

Gao J-L, Wynn TA, Chang Y, Lee E, Broxmeyer HE, Cooper S, Tiffany HL, Westphal H, Kwon-Chung J, and Murphy PM. Impaired host defense, hematopoiesis, granulomatous inflammation and type 1-type 2 cytokine balance in mice lacking CCR1. J. Exp. Med., 185, 1959-1968, 1997.