New Mechanism to Explain Role of Gene Mutations in Kidney Disease Uncovered

In nephrotic syndrome, a rare genetic kidney disorder, mutations in genes that code for certain proteins lead to a disruption of the recycling of the cell membrane have been discovered.

Novel mechanism that helps explain how certain genetic mutations give rise to a rare genetic kidney disorder called nephrotic syndrome has been mapped by researchers from the Center for Precision Disease Modeling at the University of Maryland School //of Medicine (UMSOM).

Using a drosophila (fruit fly) model, they found mutations in genes that code for certain proteins lead to a disruption of the recycling of the cell membrane. This disruption leads to an abnormal kidney cell structure and function, according to the study published this week in the Journal of the American Society of Nephrology.

Childhood Nephrotic Syndrome - Causes, Risk Factors, Symptoms, Diagnosis, Treatment & Prevention
Childhood nephrotic syndrome is a kidney disease marked by the increased levels of protein in urine. It can occur in children of any age, but it most commonly affects those aged 1 to 6 years.

‘Mutations in all eight exocyst genes could lead to nephrotic syndrome and thus should be included in the sequencing panel for genetic kidney diseases.’

Disruption of kidney cell function leads to nephrotic syndrome, a kidney disease that causes an abnormal amount of protein leaking into the urine due to a problem with the kidney's filters. It occurs in about 7 in 100,000 Americans, and though rare, it is considered one of the most common kidney diseases in children.

Nephrotic syndrome caused by genetic mutations often does not respond to the standard steroid treatment, so treatment depends on the identification of the genetic mutation that causes the disease, followed by targeted therapeutic development based on the disease mechanism. There are, however, no known treatments for the condition when it is caused by mutations in the genes examined in this study.

"Researchers have recently identified a mutation in one of the genes that codes for these proteins, called the exocyst complex, that has been linked to kidney disease," says Zhe Han, Ph.D., Associate Professor at the Department of Medicine and Director of the Center for Precision Disease Modeling at UMSOM. "However, the underlying mechanism by which the exocyst complex contributes to kidney disease had long been a mystery."

Quiz on Kidney
The kidneys are two bean-shaped organs, each about the size of a fist, and are located just below the rib cage, one on each side of your spine.

Healthy kidneys filter about half a cup of blood every minute, removing wastes and extra water to make urine. The urine flows from the kidneys to the bladder through two thin tubes of muscle called ureters, one on each side of your bladder. The bladder stores urine. The kidneys, ureters, and bladder are partof the urinary tract.

Genetic Mutations Linked to Nephrotic Syndrome Identified
The most common genetic variants were analyzed. Scientists aim to improve diagnosis and treatment for nephrotic syndrome and different types of genetic mutations linked to nephrotic syndrome have been identified.

kidneys remove wastes and extra fluid from your body. Kidneys also remove acid that is produced by the cells of your body and maintain a healthy balance of water, salts, and minerals-such as sodium, calcium, phosphorus and potassium-in your blood ().

Without this balance, nerves, muscles, and other tissues in the body may not work normally.

Susceptible Genes for Childhood Chronic Kidney Disease Discovered
New research identified the genes that make Japanese infants susceptible to steroid-sensitive nephrotic syndrome.

Kidneys also make hormones that help

Control your blood pressure
Make red blood cells
Keep your bones strong and healthy

Dr. Han's team used Drosophila as a model to better understand the mechanism by which these gene mutations potentially give rise to kidney disease. Drosophila have specialized filtration cells (nephrocytes) that closely resemble human podocytes, a type of kidney cell associated with nephrotic syndrome, both in structure and function. Using the power of fly genetics, the research team carried out a genetic screen with Drosophila and identified each of the eight exocyst genes that are required for nephrocytes to function properly.

Silencing the Drosophila exocyst genes in nephrocytes led to a disruption of a structure essential for filtering called the nephrocyte slit diaphragm. The researchers then used a transmission electron microscope to take a closer look at the ultrastructural changes, which revealed the appearance of unique electron-dense tubular structures which they named "exocyst rods".

"Therefore, the formation of the exocyst rods can be used as a new biomarker for diseases caused by genetic mutations in exocyst genes," Dr. Han said. The finding, if replicated, also has important clinical implications for patients who are screened for genetic kidney diseases.

Dr. Han and his team are currently using their Drosophila model to gain additional insight into the mechanisms regulating slit diaphragm proteins and how their disruption might contribute to the podocyte pathogenesis seen in kidney disease patients.

"This is an important finding that demonstrates the important mission of the Center for Precision Disease Modeling at the University of Maryland School of Medicine," said UMSOM Dean E. Albert Reece, MD, PhD, MBA, who is also the Executive Vice President for Medical Affairs, University of Maryland, and the John Z. and Akiko K. Bowers Distinguished Professor. "Further studies to understand this molecular mechanism could lead to a new targeted therapeutic approach that could eventually benefit patients with this devastating kidney disease."

Source-Eurekalert