The adaptive intestinal response to massive enterectomy is preserved in c-SRC-deficient mice

Richard A. Falcone, Cathy E. Shin, Christopher R. Erwin, Brad W. Warner

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

Background/Purpose: The Src family of protein tyrosine kinases has been implicated in the downstream mitogenic signaling of several ligands including epidermal growth factor (EGF). Because EGF likely plays a role in adaptation after massive small bowel resection (SBR), we tested the hypothesis that c- src is required for this important response. Methods: A 50% proximal SBR or sham operation (bowel transection or reanastomosis alone) was performed on c- src-deficient (n = 14) or wild-type (C57bl/6) mice (n = 20). The ileum was harvested on postoperative day 3 and adaptive parameters determined as changes in ileal wet weight, protein and DNA content, proliferation index, villus height, and crypt depth. Comparisons were done using analysis of variance (ANOVA), and a P value less than .05 was considered significant. Values are presented as mean ± SEM. Results: The activity of c-src was increased in the ileum of wild-type mice after SBR but remained unchanged in c-src-deficient mice. Despite this lack of increase, adaptation occurred after SBR in the c-src-deficient mice as demonstrated by increased ileal wet weight, protein and DNA content, proliferation index, villus height, and crypt depth similar to wild-type mice. Conclusions: The adaptive response of the intestine to massive SBR is preserved despite reduced activity of the c- src protein. The mitogenic signaling that characterizes intestinal adaptation and is associated with receptor activation by EGF or other growth factors probably occurs by mechanisms independent of c-src protein tyrosine kinase.

Original languageEnglish
Pages (from-to)800-804
Number of pages5
JournalJournal of Pediatric Surgery
Volume34
Issue number5
DOIs
StatePublished - May 1999
Externally publishedYes

Keywords

  • Enterectomy
  • Epidermal growth factor receptor
  • Intestinal adaptation
  • Mice
  • Short bowel syndrome
  • src kinase

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