New Insights into the Development of Epithelial Cells

Dr. Max Werth, Katharina Walentin and Professor Kai Schmidt-Ott have identified a transcription factor (grainyhead-like 2, Grhl2), which regulates the composition of the molecular “bridges” that link adjacent epithelial cells. The authors were able to demonstrate that Grhl2, via DNA-binding, directly regulates the expression of two such cell junctional molecules, E-cadherin and claudin 4 (Development, doi:10.1242/dev.055483)*.

This could be important for understanding the mechanisms of various diseases. For example, Grhl2-deficient mice die early in embryonic development and display defects of neural tube closure, including spina bifida.

Spina bifida is a common human congenital disease that is often associated with severe disabilities. Little is known about how the disease develops, and Grhl2 may be an important player in its pathogenesis.

Furthermore, the authors hypothesize that Grhl2 may also have important functions in internal organs, such as the kidney. Epithelial cells line the renal tubular system, which in humans is several kilometers long.

This system of renal tubules, together with the renal corpuscles, forms the basic structural and functional unit of the kidney – the nephron. The human kidney filters waste products from 1700 liters of blood per day, of which 180 liters are collected as primary urine and of which finally one to two liters are excreted as urine.

The studies of the authors show that Grhl2 is produced in nephron segments that are relatively impermeable to water and solutes and that fine-tune the composition of urine.

A dysfunction of Grhl2 in these cells may affect epithelial barrier formation and other cell characteristics and, thereby, contribute to various diseases, including congenital abnormalities of the kidney or the development of hypertension.

*The transcription factor grainyhead-like 2 (Grhl2) regulates molecular composition of the epithelial apical junctional complex
Max Werth1,2,*, Katharina Walentin1,2*, Annekatrin Aue1,2, Jörg Schönheit1, Anne Wuebken1, Naomi Pode-Shakked3, Larissa Vilianovitch1, Bettina Erdmann1, Benjamin Dekel3, Michael Bader1, Jonathan Barasch4, Frank Rosenbauer1, Friedrich C. Luft1,2, Kai M. Schmidt-Ott1,2,#
* these authors contributed equally
1Max-Delbrück Center for Molecular Medicine, Berlin, Germany; 2Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin, Campus Buch, Berlin, Germany, 3Department of Pediatrics and Pediatric Stem Cell Research Institute, Sheba Medical Center, Tel Hashomer, Israel, 4Department of Medicine, Columbia University College of Physicians and Surgeons, New York, USA

# Corresponding author: Prof. Dr. Kai M. Schmidt-Ott, e-mail: kai.schmidt-ott@mdc-berlin.de

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