Immunolocalization of a new intestinal antiproliferative factor in human intestinal epithelial cells

• Published in: Digestive diseases and sciences Vol. 47; no. 11; pp. 2446 - 2453
• Main Authors: Lavagna, Christian, Strup, Carine, Rampal, Agnes, Hofman, Paul, Bardon, Sylvie, Rampal, Patrick, Poirée, Jean-Claude
• Format: Journal Article
• Language: English
• Published: United States Springer Nature B.V 01.11.2002
• Subjects: Adenocarcinoma - metabolism; Adenocarcinoma - pathology; Animals; Animals, Newborn; Cell Division - physiology; Colonic Diseases - metabolism; Colonic Diseases - pathology; Colonic Neoplasms - metabolism; Colonic Neoplasms - pathology; G1 Phase - physiology; Goblet Cells - metabolism; Growth Inhibitors - analysis; Growth Inhibitors - metabolism; Growth Inhibitors - physiology; HT29 Cells; Humans; Immunohistochemistry; Intestinal Mucosa - metabolism; Intestinal Mucosa - pathology; Intestine, Small - metabolism; Intestine, Small - pathology; Membrane Proteins - analysis; Membrane Proteins - metabolism; Membrane Proteins - physiology; Mice; Microscopy, Confocal; Molecular Weight; Mucins - metabolism
• ISSN: 0163-2116; 1573-2568
• DOI: 10.1023/A:1020591405578

A new intestinal antiproliferative factor (IAF) with an approximate molecular weight of 120 kDa has been purified from the human small intestine. This factor blocks the progression of human colon adenocarcinoma cells HT-29 from the G1 to the S phase. IAF, specific of the lower part of the digestive tract, was detected rather late in mouse embryonic development. For determination of the specific intestinal cell producing IAF, long-term differentiated mucus-secreting HT-29 Cl 16E and enterocytic HT-29 Cl 19A cell lines were used. IAF is synthesized exclusively in the intestinal goblet cells; it is processed in the RER and Golgi complex before being excreted in secretory vesicles independently of mucin secretion. IAF can be considered a growth inhibitor of intestinal proliferation for the same reason as TGF-beta. However, two features differentiate it from TGF-beta: (1) the intestinal cell type synthesizing it, and (2) the delay in its expression in embryonic development. Particular interest was paid to IAF expression in pathological conditions using human colon biopsies. IAF was consistently recovered in biopsies from patients with inflammatory bowel diseases and benign tumors, but it was never detected in malignant tumors. IAF could represent a marker of colon cancer owing to its absence from malignant tumors.