TY - JOUR
T1 - Effect of Massive Small Bowel Resection on the Bax/Bcl-w Ratio and Enterocyte Apoptosis
AU - Stern, Lawrence E.
AU - Falcone, Richard A.
AU - Kemp, Christopher J.
AU - Stuart, Lorie A.
AU - Erwin, Christopher R.
AU - Warner, Brad W.
N1 - Funding Information:
The Bcl-2 family of proteins plays a significant role in the regulation of several apoptotic pathways including those involved with the mitochondria. The Bcl-2 family consists of both pro-survival and pro-apoptotic gene members that share at least one of the highly conserved Bcl-2 homology domains (BH1, BH2, BH3, and BH4). Immunostaining of the en-terocyte crypts has revealed moderate to intense quantities of the pro-apoptotic Bax protein, whereas From the Division of Pediatric Surgery,C hildren's Hospital Medical Center, and the Department of Surgery, Universityo f Cincinnati College of Medicine, Cincinnati, Ohio. Supported by grants F32 DK09882 (Dr. Stern) and RO-1 DK53234 (Dr. Warner) from the National Institutes of Health and by a grant from the Children's Hospital Campaign for Children Fund, Children's Hospital Medical Center, Cincinnati, Ohio. Presented at the FortiethAnnu~lM eeting of The SoCietyf or Surgeryo f the AlimentaryT ract, Orlando, Fla., May 16-19, 1999. Reprint requests: Brad W. Warner, M.D., Division of Pediatric Surgery,C hildren's Hospital Medical Center, 3333 Burnet Ave., Cincinnati, OH 45229-3039. e-mail: Brad.Warner@uc.edu
PY - 2000
Y1 - 2000
N2 - Following small bowel resection (SBR), the remnant intestine undergoes adaptation. Enterocyte proliferation is increased and counterbalanced by increased rates of apoptosis. To elucidate a mechanism for increased enterocyte apoptosis, this study tested the hypothesis that the ratio between pro-apoptotic Bax and pro-survival Bcl-w correlates with the apoptosis that occurs following SBR. Mice (C57B1/6; n = 76) underwent a 50% proximal SBR or sham operation. After 12 hours and 1, 2, 3, and 7 days, the ileum was removed, the apoptotic index (apoptotic bodies/crypt) was recorded, and the messenger RNA and protein for Bax and Bcl-w were quantified. The apoptotic index was equivalent in the sham and SBR mice at 12 hours; however, it was significantly elevated following SBR at every other day measured. The ratio of Bax to Bcl-w messenger RNA relative to sham operation increased after SBR at 24 hours, decreased by day 3, and returned to baseline levels by 1 week. The protein ratio showed an increase by day 1, which remained elevated through day 7. An augmented ratio of Bax to Bcl-w messenger RNA and protein corresponded with the increase in enterocyte apoptosis. Alterations in the expression ratio of these genes may play a role in establishing a new homeostatic set point between proliferation and apoptosis during adaptation.
AB - Following small bowel resection (SBR), the remnant intestine undergoes adaptation. Enterocyte proliferation is increased and counterbalanced by increased rates of apoptosis. To elucidate a mechanism for increased enterocyte apoptosis, this study tested the hypothesis that the ratio between pro-apoptotic Bax and pro-survival Bcl-w correlates with the apoptosis that occurs following SBR. Mice (C57B1/6; n = 76) underwent a 50% proximal SBR or sham operation. After 12 hours and 1, 2, 3, and 7 days, the ileum was removed, the apoptotic index (apoptotic bodies/crypt) was recorded, and the messenger RNA and protein for Bax and Bcl-w were quantified. The apoptotic index was equivalent in the sham and SBR mice at 12 hours; however, it was significantly elevated following SBR at every other day measured. The ratio of Bax to Bcl-w messenger RNA relative to sham operation increased after SBR at 24 hours, decreased by day 3, and returned to baseline levels by 1 week. The protein ratio showed an increase by day 1, which remained elevated through day 7. An augmented ratio of Bax to Bcl-w messenger RNA and protein corresponded with the increase in enterocyte apoptosis. Alterations in the expression ratio of these genes may play a role in establishing a new homeostatic set point between proliferation and apoptosis during adaptation.
KW - Apoptosis
KW - Bax
KW - Bcl-w
KW - Intestine
KW - Short bowel syndrome
UR - http://www.scopus.com/inward/record.url?scp=0033627580&partnerID=8YFLogxK
U2 - 10.1016/S1091-255X(00)80038-4
DO - 10.1016/S1091-255X(00)80038-4
M3 - Article
C2 - 10631368
AN - SCOPUS:0033627580
SN - 1091-255X
VL - 4
SP - 93
EP - 100
JO - Journal of Gastrointestinal Surgery
JF - Journal of Gastrointestinal Surgery
IS - 1
ER -