Apoptosis and the pattern of DNase I expression following massive small bowel resection

被引:26
作者
Falcone, RA [1 ]
Stern, LE [1 ]
Kemp, CJ [1 ]
Shin, CE [1 ]
Erwin, CR [1 ]
Warner, BW [1 ]
机构
[1] Univ Cincinnati, Childrens Hosp, Coll Med,Dept Surg, Div Pediat Surg, Cincinnati, OH 45229 USA
关键词
deoxyribonuclease I; apoptosis; intestinal adaptation; mouse;
D O I
10.1006/jsre.1999.5649
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introduction. Following massive small bowel resection (SBR), histologic evidence of increased enterocyte apoptosis has been demonstrated in several animal models. Deoxyribonuclease I (DNase I) is requisite for intranuclear cleavage of DNA during apoptosis; we therefore hypothesized that the expression of this gene would be increased following SBR. Methods. Male ICR mice underwent either 50% proximal SBR or sham surgery (bowel transection/reanastomosis). After 12 h and 1, 3, and 7 days, rates of enterocyte proliferation and apoptosis were recorded as well as DNase I mRNA expression and activity. Results. Adaptation after SBR was confirmed at each time point by increased proliferation. Enterocyte proliferation was increased by 12 h and apoptosis was increased by 24 h and remained elevated through Day 7, When compared with sham-operated mice, SBR resulted in a twofold increase in both DNase I expression and activity at 24 h postoperatively, which returned to baseline by Postoperative Day 3. Conclusions. DNase I expression and activity are increased early following massive SBR but return to baseline despite persistent increased rates of enterocyte apoptosis and proliferation. This enzyme may be important in the early induction of apoptosis following massive SBR, but not once anew set point has been established in the balance between the rate of enterocyte production and enterocyte loss. (C) 1999 Academic Press.
引用
收藏
页码:218 / 222
页数:5
相关论文
共 25 条
[1]   IDENTIFICATION OF DEOXYRIBONUCLEASE-II AS AN ENDONUCLEASE INVOLVED IN APOPTOSIS [J].
BARRY, MA ;
EASTMAN, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 300 (01) :440-450
[2]  
COHEN JJ, 1984, J IMMUNOL, V132, P38
[3]   A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD [J].
Enari, M ;
Sakahira, H ;
Yokoyama, H ;
Okawa, K ;
Iwamatsu, A ;
Nagata, S .
NATURE, 1998, 391 (6662) :43-50
[4]  
HALL PA, 1994, J CELL SCI, V107, P3569
[5]   Enterocyte Apoptosis Is Increased Following Small Bowel Resection [J].
Helmrath M.A. ;
Erwin C.R. ;
Shin C.E. ;
Warner B.W. .
Journal of Gastrointestinal Surgery, 1998, 2 (1) :44-49
[6]   The EGF\EGF-receptor axis modulates enterocyte apoptosis during intestinal adaptation [J].
Helmrath, MA ;
Shin, CE ;
Erwin, CR ;
Warner, BW .
JOURNAL OF SURGICAL RESEARCH, 1998, 77 (01) :17-22
[7]   Intestinal adaptation is enhanced by epidermal growth factor independent of increased ileal epidermal growth factor receptor expression [J].
Helmrath, MA ;
Shin, CE ;
Erwin, CR ;
Warner, BW .
JOURNAL OF PEDIATRIC SURGERY, 1998, 33 (07) :980-984
[8]   A defective EGF-receptor in waved-2 mice attenuates intestinal adaptation [J].
Helmrath, MA ;
Erwin, CR ;
Warner, BW .
JOURNAL OF SURGICAL RESEARCH, 1997, 69 (01) :76-80
[9]  
Helmrath MA, 1996, J AM COLL SURGEONS, V183, P441
[10]  
LACKS SA, 1981, J BIOL CHEM, V256, P2644