Published October 30, 2009 | Version v1
Journal article

Schlafen-3: A novel regulator of intestinal differentiation

  • 1. Department of Internal Medicine, Wayne State University, Detroit, MI 48201 (United States)
  • 2. Veterans Affairs Medical Center, Wayne State University, Detroit, MI 48201 (United States)
  • 3. Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201 (United States)

Description

Schlafen-3 (Slfn-3), a novel gene, has been shown to be a negative regulator of proliferation. The current investigation was undertaken to determine whether Slfn-3 might play a role in regulating cellular differentiation. Butyric acid, a short chain fatty acid, which induced differentiation of intestinal cells as evidenced by increased alkaline phosphatase (ALP) activity in the rat small intestinal IEC-6 cells, also produced a marked increase in Slfn-3 expression. Furthermore, overexpression of Slfn-3 caused stimulation of ALP activity in IEC-6 cells, which was exacerbated by butyrate. On the other hand, downregulation of Slfn-3 by slfn-3-si-RNA greatly attenuated the butyrate-mediated induction of differentiation of IEC-6 cells. Additionally, we observed that increased expression of Slfn-3 in colon cancer HCT-116 cells stimulated TGF-β expression and modulated expression of its downstream effectors as evidenced by increased expression of p27kip1 and downregulation of CDK-2. In addition, Slfn-3 increases E-cadherin expression but downregulates β-catenin. In conclusion, our data show that Slfn-3 plays a critical role in regulating intestinal mucosal differentiation. Furthermore our data also show that TGF-β signaling pathway plays an important role in mediating slfn-3 induced differentiation.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2009.08.094

Additional details

Identifiers

DOI
10.1016/j.bbrc.2009.08.094;
PII
S0006-291X(09)01672-6;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
388
Journal Issue
4
Journal Page Range
p. 752-756
ISSN
0006-291X
CODEN
BBRCA9

INIS

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.