RTG 2408 - Maladaptive processes across physiological barriers in chronic diseases

Project 9

Unfolded protein response (UPR) in diabetic kideny disease and H. pylori infected gastric mucosa

 

SK

Shruthi Krishnan

PhD Student

               YY

Yanfei Yu

PhD Student

 

BI_n

Prof. Dr. Berend Isermann

Project Leader

 

MN_n

Prof. Dr. Michael Naumann

Project Leader

Diabetic nephropathy (dNP), now the most common cause of chronic renal disease, is characterized by dysfunctional barriers in the glomerular and tubular compartments. A common cell type found in both renal compartments are pericytes, which interact with epithelial (EpiC) and endothelial (EndoC) cells. Maladaptive pericyte activation impairs barrier function and promotes kidney fibrosis, a common final pathway in kidney damage. Targeting pericyte function may allow protection of both renal compartments. However, specific strategies to target pericytes are currently lacking. TEM1 (tumor endothelial marker 1, CD248, or endosialin) is a protein expressed by pericytes in various organs, including the kidney and the stomach. Expression of TEM1 is high during development in tumors and during inflammatory diseases. In a clinical study low TEM1 expression by cancer associated fibroblast correlates with increased survival of gastric cancer patients. However, the mechanisms underlying TEM1-dependent effects remain poorly defined. In cooperative work (Project P7) we analyzed TEM1 regulation and the unfolded protein response (UPR) and established a role of TEM1 in renal pericytes in the context of dNP. We hypothesize that pericyte derived TEM1 co-ordinately regulates barrier function in chronic diseases. Specifically, we define the molecular mechanism and functional consequences of intracellular signaling via TEM1 between pericytes and barrier-defining epithelial cells, and conduct a structure function analyses of TEM1 to identify the molecular structures required for barrier regulation to determine whether modulating TEM1 function allows to rescue epithelial cells and thus barrier function. Two PhD students jointly address questions about the regulation of the UPR in the context of renal cells (Shruthi Krishnan) and H. pylori-infected gastric mucosal cells (Yanfei Yu).

 

TP9_neu

 

UPR regulation in DKD and H. pylori infection

(A) TEM-1 expressing cells in the kidney (blue; mesangial cells, top, and peritubular pericytes, bottom) interact with endothelial cells (red), podocytes (yellow, top), and tubular cells (yellow, bottom). (B) Schematic diagram of UPR signalling.

Photos: M. Schubert/University Hospital Magdeburg

Last Modification: 30.05.2022 - Contact Person:

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