IL-6 protects enterocytes from hypoxia-induced apoptosis by induction of bcl-2 mRNA and reduction of fas mRNA

被引:45
|
作者
Rollwagen, F. M.
Madhavan, S.
Singh, A.
Li, Y. -Y.
Wolcott, K.
Maheshwari, R.
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Pathol, Bethesda, MD 20814 USA
[2] Birla Inst Technol & Sci, Pilani, Rajasthan, India
[3] Henry M Jackson Fdn, Rockville, MD USA
[4] Uniformed Serv Univ Hlth Sci, Biomed Instrumentat Ctr, Bethesda, MD 20814 USA
关键词
IL-6; tissue culture; intestinal epithelial cells;
D O I
10.1016/j.bbrc.2006.07.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-6 (IL-6) has been shown to rescue enterocytes from hypoxia-induced apoptosis when given orally following hemorrhagic shock. In vitro models using an intestinal epithelial cell line (IEC-6) cultured with lipopolysaccharide (LPS) under low O-2 conditions, to mimic intestinal conditions, show that these cells also undergo apoptosis, which can be reduced by subsequent culture with IL-6. To examine further the mechanisms of rescue, we cultured normal rat intestinal epithelial cells (IEC-6) under both normoxic and hypoxic conditions and analyzed their responses to LPS and IL-6. We showed that IEC-6 expressed IL-6 receptor on its surface. Further, IEC-6 cells could be rescued from hypoxia-induced apoptosis by co-culture with IL-6. RNase protection assay (RPA) examination revealed that under hypoxic conditions, IEC-6 cells that were resistant to apoptosis showed reduced fas expression and increased bcl-2 expression after co-culture with LPS + IL-6. Published by Elsevier Inc.
引用
收藏
页码:1094 / 1098
页数:5
相关论文
共 50 条
  • [1] IL-6 rescues enterocytes from hemorrhage induced apoptosis in vivo and in vitro by a bcl-2 mediated mechanism
    Rollwagen, FM
    Yu, ZY
    Li, YY
    Pacheco, ND
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 89 (03): : 205 - 213
  • [2] Allopurinol protects enterocytes from hypoxia-induced apoptosis in vivo - Discussion
    Choo, D
    Albuquerque, RG
    [J]. JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 2002, 53 (03): : 420 - 421
  • [3] Nicorandil regulates Bcl-2 family proteins and protects cardiac myocytes against hypoxia-induced apoptosis
    Nishikawa, S
    Tatsumi, T
    Shiraishi, J
    Matsunaga, S
    Takeda, M
    Mano, A
    Kobara, M
    Keira, N
    Okigaki, M
    Takahashi, T
    Matsubara, H
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2006, 40 (04) : 510 - 519
  • [4] bcl-2 Prolongs neuronal survival during hypoxia-induced apoptosis
    Banasiak, KJ
    Cronin, T
    Haddad, GG
    [J]. MOLECULAR BRAIN RESEARCH, 1999, 72 (02): : 214 - 225
  • [5] Bcl-2 protects from lethal hepatic apoptosis induced by an anti-Fas antibody in mice
    Lacronique, V
    Mignon, A
    Fabre, M
    Viollet, B
    Rouquet, N
    Molina, T
    Porteu, A
    Henrion, A
    Bouscary, D
    Varlet, P
    Joulin, V
    Kahn, A
    [J]. NATURE MEDICINE, 1996, 2 (01) : 80 - 86
  • [6] BCL-2 PROTECTS FROM LETHAL HEPATIC APOPTOSIS INDUCED BY THE ANTI-FAS ANTIBODY IN MICE
    LACRONIQUE, V
    MIGNON, A
    FABRE, M
    BOUSCARY, D
    ROUQUET, N
    JOULIN, V
    VARLET, P
    KAHN, A
    [J]. HEPATOLOGY, 1995, 22 (04) : 483 - 483
  • [7] Selenium protects the hypoxia induced apoptosis in neuroblastoma cells through upregulation of Bcl-2
    Sarada, S. K. S.
    Himadri, P.
    Ruma, D.
    Sharma, S. K.
    Pauline, T.
    Mrinalini
    [J]. BRAIN RESEARCH, 2008, 1209 : 29 - 39
  • [8] Bcl-2 silencing attenuates hypoxia-induced apoptosis resistance in pulmonary microvascular endothelial cells
    Yongmei Cao
    Zhen Jiang
    Zhen Zeng
    Yujing Liu
    Yuchun Gu
    Yingying Ji
    Yupeng Zhao
    Yingchuan Li
    [J]. Apoptosis, 2016, 21 : 69 - 84
  • [9] Hypoxia-Induced Modulation of Apoptosis and BCL-2 Family Proteins in Different Cancer Cell Types
    Sermeus, Audrey
    Genin, Marie
    Maincent, Amelie
    Fransolet, Maude
    Notte, Annick
    Leclere, Lionel
    Riquier, Helene
    Arnould, Thierry
    Michiels, Carine
    [J]. PLOS ONE, 2012, 7 (11):
  • [10] Hypoxia-induced apoptosis is blocked by adrenomedullin via upregulation of Bcl-2 in human osteosarcoma cells
    Wu, Xue-Yuan
    Hao, Cui-Pei
    Ling, Ming
    Guo, Chi-Hua
    Ma, Wei
    [J]. ONCOLOGY REPORTS, 2015, 34 (02) : 787 - 794