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[MMP-9 expression profile in inflammatory cells of Mip-1alpha knockout mice and Mip-1alpha receptor knockout mice].

AbstractOBJECTIVE:
To explore the MMP-9 expression profile in peritoneal inflammatory macrophages and granulocytes in Mip-1alpha-, CCR1- and CCR5-deficient mice.
METHODS:
In sodium thioglycolate-induced murine peritonitis models, peritoneal macrophages and granulocytes were harvested, identified and purified from WT mice and Mip-1alpha-, CCR1-, CCR5-deficient mice. The RT-PCR was applied to evaluate the expression of MMP-9 in macrophages and granulocytes of different group of mice.
RESULTS:
The expressions of MMP-9 of macrophages in Mip-1alpha-, CCR1-, CCR5-deficient mice were significantly lower than that of WT mice (P<0.05); MMP-9 expression of granulocytes in Mip-1alpha-, CCR5-deficient mice were also significantly lower than that of WT mice (P<0.05), while the MMP-9 expression of granulocytes in CCR1-deficient mice was significant higher than that of WT mice.
CONCLUSION:
Deletion of Mip-1alpha and CCR5 could reduce the MMP-9 expression in both macrophages and granulocytes, while deletion of CCR1 could reduce MMP-9 expression in macrophages but increase MMP-9 expression in granulocytes.
AuthorsYu Wu, Naofumi Mukaida, Ting Liu, Yong-qian Jia, Huan-ling Zhu, Yi-ming Yang, Cai-gang Xu, Zhang-xue Hu
JournalSichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition (Sichuan Da Xue Xue Bao Yi Xue Ban) Vol. 40 Issue 3 Pg. 374-7 (May 2009) ISSN: 1672-173X [Print] China
PMID19626984 (Publication Type: Journal Article)
Chemical References
  • Chemokine CCL3
  • RNA, Messenger
  • Receptors, CCR1
  • Receptors, CCR5
  • Matrix Metalloproteinase 9
  • Mmp9 protein, mouse
Topics
  • Animals
  • Chemokine CCL3 (genetics)
  • Female
  • Granulocytes (metabolism)
  • Macrophages, Peritoneal (metabolism)
  • Matrix Metalloproteinase 9 (genetics, metabolism)
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • RNA, Messenger (genetics, metabolism)
  • Receptors, CCR1 (genetics)
  • Receptors, CCR5 (genetics)

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