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Beta Cells

Exploring Beta Cell Regeneration in Treating Type 1 Diabetes

In individuals with type 1 diabetes (T1D), the body’s immune system mistakenly destroys insulin-producing beta cells necessary for managing blood sugar. Instead, patients must constantly monitor their own blood glucose levels and administer the proper dosage of insulin as necessary. In individuals without T1D, the pancreas does this automatically.

Some of the challenges that researchers have faced in trying to treat or cure T1D through cellular means is that the body may still reject these cells, there may be a shortage of donor cells, or the process of creating necessary beta cells can be complex. However, researchers at the Diabetes Research Institute at the University of Miami Miller School of Medicine may have found an effective way of using the body’s existing cell supply to generate insulin-producing beta cells.

The researchers identified the exact location in the body of progenitor cells with the ability to develop into beta cells. When stimulated by bone morphogenetic protein 7 (BMP-7), a naturally occurring growth factor, the pancreatic cells differentiated into the necessary beta cells. This discovery could lead to a significant supply of new beta cells within patients’ own bodies, eliminating the need for donor cells and curbing other immune-related challenges of treatment.

This process still requires more in-depth study, but it could lead the way to new regenerative medicine strategies that stimulate insulin production more naturally. The researchers are currently exploring options to reduce the need for lifelong anti-rejection drugs by enhancing immune tolerance of the newly created cells.

This study is another step toward advancing the treatment of T1D and providing patients with more options for care. The more scientists learn about the causes and effects of T1D, the more they can target approaches to treatment.

The Diabetes Research Connection (DRC) stays abreast of the latest developments in the field and encourages novel research projects by early-career scientists focused on T1D. The DRC raises funds through contributions by individuals, organizations, and foundations to support the advancement of these studies. Find out how you can get involved by visiting http://diabetesresearchconnection.org.

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OUR PROJECTS

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Role of the integrated stress response in type 1 diabetes pathogenesis
In individuals with type 1 diabetes (T1D), the insulin-producing beta cells are spontaneously destroyed by their own immune system. The trigger that provokes the immune system to destroy the beta cells is unknown. However, accumulating evidence suggest that signals are perhaps first sent out by the stressed beta cells that eventually attracts the immune cells. Stressed cells adapt different stress mitigation systems as an adaptive response. However, when these adaptive responses go awry, it results in cell death. One of the stress response mechanisms, namely the integrated stress response (ISR) is activated under a variety of stressful stimuli to promote cell survival. However, when ISR is chronically activated, it can be damaging to the cells and can lead to cell death. The role of the ISR in the context of T1D is unknown. Therefore, in this DRC funded study, we propose to study the ISR in the beta cells to determine its role in propagating T1D.
Wearable Skin Fluorescence Imaging Patch for the Detection of Blood Glucose Level on an Engineered Skin Platform
zhang
A Potential Second Cure for T1D by Re-Educating the Patient’s Immune System
L Ferreira
Validating the Hypothesis to Cure T1D by Eliminating the Rejection of Cells From Another Person by Farming Beta Cells From a Patient’s Own Stem Cells
Han Zhu
Taming a Particularly Lethal Category of Cells May Reduce/Eliminate the Onset of T1D
JRDwyer 2022 Lab 1
Can the Inhibition of One Specific Body Gene Prevent Type 1 Diabetes?
Melanie
Is Cholesterol Exacerbating T1D by Reducing the Functionality and Regeneration Ability of Residual Beta Cells?
Regeneration Ability of Residual Beta Cells
A Call to Question… Is T1D Caused by Dysfunctionality of Two Pancreatic Cells (β and α)?
Xin Tong
Novel therapy initiative with potential path to preventing T1D by targeting TWO components of T1D development (autoimmune response and beta-cell survival)
flavia pecanha