Key Form of Tau Protein Identified for Understanding and Treating Alzheimer’s Disease

Health & Medicine


Key Protein Identified for Understanding and Treating Alzheimer's Disease

Knockout of Tau Causes Mill Deficits in Neurite Growth and Ais Formation But Does Not Alter Neuronal Activity. CREDIT: Alzheimer’s & Dementia (2025). DOI: 10.1002/ALZ.14403,

The Research Team at the University of Cologne has made a Significant Breakthrough in Understanding the Role of the Tau Protein in Alzheimer’s Disease. Using Human Induced Pluripotent Stem Cells (IPSCS), The International Team has Been Able To Show That a Specific Form of the Tau Protein, Known As The 1N4R Isoform, is Responsible for Mediating The Toxic Effects of Protein Clumps in Human Brain Cells.

The Study is published In the Alzheimer’s & Dementia Journal Under the Title “The Tau Isoform 1N4R Conferences Vulnerability of Mapt Knockout Human IPSC-Deriveed Neurons to Amyloid Beta and Phosphoryladed Tau-Handiced Neuronal Dysfunction.” It was LED by Dr. Hans Zempel from the Institute of Human Genetics, which is also the group Leader in the Career Advancement Program (Cap) at the Center for Molecular Medicine Cologne (CMMC) of the University of Cologne and University Hospital Cologne.

If Person Suffers from Alzheimer’s Disease, Certain Proteins Accumulate in Brain Cells, Forming Clumps That Restict Normal Cell Function or Even Call to Die. Dr. Sarah Buchholz and Dr. Zempel’s Team have used state-of-the-art techniques such as crispr/cas9 gene editing and live-cell imaging in human Induced pluripotent cells (iPSCS) to demonstrate that the 1n4r tau isiform is responsive for the patholic effects on the Cell.

IPSCS are human stem cells that are generated from other cells. Example, Skin Cells can be reprogrammed into ipscs and from there transformed into brain cells (neurons). The Researchers Testd Different Forms of the Tau Protein by Expressing Them Specifically in Nerve Cells. In This Way, The Researchers Were Aple To Analyze How Each Protein Isoform Affects The Cell.

According to Dr. Buchholz, First Author of the Study, “This Study Representations A Significant Advance in Helping Us to Underser The Mechanisms of Alzheimer’s Disease. By Identifying 1n4r as Key Protein, We Have Discoved A Potential New Target for Future Treatments.”

The Study’s Interdisciplinary Approach Not Only Helps to Better Understand Alzheimer’s Disease But Also Demonstrates The Importance of Human Cell Models In Neurodegenerative Research. Further Studies Are Needed to Translate The Results of This Study Into Clinical Application, in Private to Validate The Results In Adequate Animal Models and To Develop Specific Therapeutics That Will Intervene In This Process.

More information:
Sarah Buchholz et al. The Tau Isoform 1N4R Conferences Vulnerability of Mapt Knockout Human IPSC-Deriveed Neurons to Amyloid beta and phosphoryed Tau-dendiced Neuronal Dysfunction, Alzheimer’s & Dementia (2025). DOI: 10.1002/ALZ.14403, alz-journals.onlinelibrary.wil… ll/10.1002/alz.14403

PROVIDED BY UNIVERSITY OF COLOGNE


Citation: Key Form of Tau Protein Identified for Understanding and Treating Alzheimer’s Disease (2025, February 28) Retrieved 28 February 2025 from

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