Systemic and local evidence of increased Fas-mediated apoptosis in ulcerative colitis.

Abstract

BACKGROUND AND AIMS:

Recent studies suggest that Fas-mediated apoptosis is involved in the pathogenesis of inflammatory bowel disease (IBD). This study was conducted to clarify whether soluble forms of Fas (sFas) and Fas ligand (sFasL) are concerned with inflammation in IBD.

METHODS AND PATIENTS:

Concentration of serum sFas and sFasL was measured by enzyme-linked immunosorbent assay in 10 patients with ulcerative colitis (UC), 10 with Crohn's disease (CD) in both active and remission stages, and 20 controls. Expression of Fas and sFas in colonic mucosa was examined by western blot. Distribution of Fas and FasL in colonic mucosa was examined by immunohistochemistry in 20 UC, 20 CD, and 10 non-IBD colitis patients and in 10 controls. Apoptotic cells were examined by TUNEL.

RESULTS:

Concentration of systemic sFas was significantly lower in active UC than controls. The number of FasL-containing cells was significantly higher in active UC than in remission UC, non-IBD colitis, and controls. Apoptotic cells were increased in active UC.

CONCLUSIONS:

Our results demonstrate that systemic and local Fas-mediated apoptosis is promoted in UC, which might be involved in the pathogenesis in UC.

• Authors: Michihiro Yukawa, Masahiro Iizuka, Yasuo Horie, Kazuo Yoneyama, Tomoyuki Shirasaka, Hiroaki Itou, Masafumi Komatsu, Tsuneo Fukushima, Sumio Watanabe
• Journal: International journal of colorectal disease (Int J Colorectal Dis) Vol. 17 Issue 2 Pg. 70-6 (Mar 2002) ISSN: 0179-1958 [Print] Germany
• PMID: 12014424 (Publication Type: Journal Article)

Chemical References

• FASLG protein, human
• Fas Ligand Protein
• Membrane Glycoproteins
• fas Receptor

Topics

• Apoptosis
• Colitis, Ulcerative (metabolism, pathology, physiopathology)
• Colon (chemistry, pathology)
• Crohn Disease (metabolism, physiopathology)
• Enzyme-Linked Immunosorbent Assay
• Fas Ligand Protein
• Humans
• Immunohistochemistry
• In Situ Nick-End Labeling
• Intestinal Mucosa (chemistry, pathology)
• Lymphocytes (metabolism)
• Membrane Glycoproteins (analysis, physiology)
• fas Receptor (analysis, physiology)