Total parenteral nutrition-induced apoptosis in mouse intestinal epithelium: Modulation by keratinocyte growth factor

被引:24
作者
Wildhaber, BE [1 ]
Yang, H [1 ]
Teitelbaum, DH [1 ]
机构
[1] Univ Michigan, Pediat Surg Sect, CS Mott Childrens Hosp, Dept Surg, Ann Arbor, MI 48109 USA
关键词
keratinocyte growth factor; intestinal epithelial cells; TPN; apoptosis; Bcl-2; proteins;
D O I
10.1016/S0022-4804(03)00160-4
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Total parenteral nutrition (TPN) induces epithelial cell (EC) apoptosis. Keratinocyte growth factor (KGF) increases EC growth; however, little is known of its effect on apoptosis. This study aimed to determine the effect of recombinant human KGF (rHuKGF) on small bowel EC apoptosis. We further determined mRNA expression of Bcl-2 family members (major mediators of epithelial cell apoptosis) with TPN and whether KGF administration influences Bcl-2 family expression in EC. Methods. C57BL/6J mice (n = 6/group) received oral feeding (Control); TPN; or TPN plus daily intravenous rHuKGF (TPN+KGF). After 7 days, intestines were harvested and EC isolated. Villus height was determined by microscopy and EC proliferation by immunohistochemistry using incorporation of 5-bromodeoxyuridine (BrdU). Apoptosis was identified by Annexin V as well as by TUNEL staining. EC mRNA expression of Bcl-2 family members was measured by reverse-transcriptase polymerase chain reaction and Bcl-2 protein level by immunoblot analysis. Results. Villus height in Controls was 310 +/- 42 mum. This decreased with TPN to 210 +/- 45 mum; however, villus height was preserved in TPN + KGF mice (273 +/- 39 mum). EC proliferation rates decreased significantly in TPN mice, and this decline was prevented by administration of rHuKGF. EC apoptotic rate in Controls was 14.4 +/- 5.1%; TPN administration resulted in doubling of largely prevented TPN-induced EC apoptosis (29.4 +/- 11.3%) rHuKGF administration largely pre vented TPN-induced EC apoptosis (17.2 +/- 5.6%). Pro. apoptotic Bcl-2 members changed minimally with TPN or rHuKGF; however, the anti-apoptotic Bcl-2 changed significantly: Control 0.78 +/- 0.24; TPN 0.10 +/- 0.13; rHuKGF administration prevented the decline in Bcl-2 expression observed with TPN (0.76 +/- 0.36). EC Bcl-2 protein levels were: Control 0.16 +/- 0.13; TPN 0.18 +/- 0.16; and TPN+KGF 0.47 +/- 0.19. Conclusion. TPN-induced apoptosis was associated with decreased Bcl-2 mRNA expression. rHuKGF decreased TPN-induced EC apoptosis and increased Bcl-2 expression. rHuKGF administration may have benefit inpatients on TPN. (C) 2003 Elsevier Inc. All rights reserved.
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页码:144 / 151
页数:8
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