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New Discovery Reveals Connection Between Chromosomal Centromeres and the Immune System

New Discovery Reveals Connection Between Chromosomal Centromeres and the Immune System

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Scientists have discovered a novel connection between chromosomal centromeres and the immune system, opening new possibilities for immunotherapy research and cancer treatment.

2 min read

Recent groundbreaking research has uncovered a direct link between centromeres—the critical regions of chromosomes responsible for proper cell division—and the immune response. Traditionally, centromeres are known for their role in ensuring accurate chromosome segregation during cell division. However, scientists from Hannover Medical School (MHH), the Institut Curie in Paris, and other collaborating institutions have discovered that these chromosome regions also play a vital role in immune activation.

This discovery stems from studies involving herpes simplex virus type 1 (HSV-1), which is known for causing cold sores and its ability to penetrate the cell nucleus. Researchers found that HSV-1 can disrupt centromere stability, leading to a unique process where the DNA in these regions undergoes amplified replication. This unusual activity is recognized by the cell’s immune mechanisms, triggering a systemic antiviral response.

The team led by Prof. Dr. Lars Dölken utilized innovative viral mutants to explore this process. They observed that when viruses hijack the cell nucleus, they destabilize the centromeres, prompting the cell to activate its immune defenses. This process not only highlights a novel aspect of cellular biology but also offers promising avenues for developing new immunotherapies for viral infections and cancers.

The insights gained from this research could potentially pave the way for novel treatments that leverage the immune system's ability to detect and respond to chromosomal abnormalities caused by viruses or tumor cells. The work has been published in the journal lle9 and represents a significant step forward in understanding the intersection of chromosomal stability and immune activation.

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