ApoE deficiency promotes colon inflammation and enhances the inflammatory potential of oxidized-LDL and TNF-α in primary colon epithelial cells

نویسندگان

  • Ali H. El-Bahrawy
  • Abdelmetalab Tarhuni
  • Hogyoung Kim
  • Venkat Subramaniam
  • Ilyes Benslimane
  • Zakaria Y. Abd Elmajeed
  • Samuel C. Okpechi
  • Mohamed A. Ghonim
  • Ramadan A.M. Hemeida
  • Amira M. Abo-yousef
  • Gamal A. El-Sherbiny
  • Ihab T. Abdel-Raheem
  • Jong Kim
  • Amarjit S. Naura
  • A. Hamid Boulares
چکیده

Although deficiency in Apolipoprotein E (ApoE) is linked to many diseases, its effect on colon homeostasis remains unknown.  ApoE appears to control inflammation by regulating NF-kB.  This study was designed to examine whether ApoE deficiency affects factors of colon integrity in vivo and given the likelihood that ApoE deficiency increases oxidized lipids and TNF-α, this study also examined whether such deficiency enhances the inflammatory potential of oxidized-LDL (oxLDL) and TNF-α, in colon epithelial cells in vitro   Here we show that ApoE deficiency is associated with chronic inflammation systemically and in colonic tissues as assessed by TNF-α levels.  Increased colon TNF-α mRNA coincided with a substantial increase in cyclooxygenase (COX)-2.  ApoE deficiency enhanced the potential of oxLDL and TNF-a to induce COX-2 expression as well as several other inflammatory factors in primary colon epithelial cells.   Interestingly, oxLDL enhanced TGF-β expression only in ApoE-/-, but not in wild-type, epithelial cells.  ApoE deficiency appears to promote COX-2 expression enhancement through a mechanism that involves persistent NF-κB nuclear localization, PI3 and p38 MAP kinases but independently of Src.  In mice, ApoE deficiency promoted a moderate increase in crypt length, which was associated with opposing effects of an increase in cell proliferation and apoptosis at the bottom and top of the crypt, respectively.   : Our results support the notion that ApoE plays a central role in colon homeostasis and that ApoE deficiency may constitute a risk factor for colon pathologies.

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عنوان ژورنال:

دوره 36  شماره 

صفحات  -

تاریخ انتشار 2016