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Gene & Protein in Disease                                             β-cell regeneration and stem cell niche











































            Figure 1. Mechanisms of signaling pathways controlling β-cell proliferation induced by phytochemicals. Upregulation/activation is represented by black
            arrows, while inhibition is indicated by red arrows. Reprinted from Kimani et al. 9

            although this is less certain in humans. Under specific   cellular function. Current research aims to enhance cell
            conditions, pancreatic progenitor cells may become active.   efficiency to delay or reverse diabetes onset. Therapeutic
            Although there are disagreements, artemisinins and GABA   techniques include direct islet transplantation, implantation
            can stimulate cell-to-cell conversion (Figure 2). Ongoing   of progenitors/stem cells into  β-cells, replication of pre-
            research on FOXO1 inhibition shows promise, as deletion   existing  β-cells, and stimulation of endogenous  β-cell
            of this gene allows intestinal endocrine progenitors to   progenitors. Attention has been drawn to the discovery
            transform into insulin-producing cells in the gut. Small-  of cellular signaling networks linked to genes or proteins
            molecule inhibitors of non-canonical IB kinases, such as   playing integral roles in diabetes (Figure  3). However,
            TKB1 and IKK, have been found to induce cell regeneration   unresolved pathways and molecules associated with
            in various species. Mammalian islets primarily include   β-cells, particularly in humans, contribute to a lack of
            β-cells that express TBK1, with expression levels elevated   understanding of their specialized functions, underscoring
            during exposure to diabetogenic insults, such as T2D. In   the need for further research. The majority of cell pathways
            streptozotocin-induced diabetic mice, PIAA expedited the   and chemicals, as well as their specialized roles, are still
            restoration of functioning β-cells and increased expression   elusive, especially in humans. Therefore, additional studies
            of cell cycle regulatory molecules and cell differentiation   are warranted to further understand the cellular processes
            markers in response to diabetogenic stimuli.       governing human  β-cell proliferation and its underlying
                                                               mechanisms and roles.
              Pancreatic cells play a crucial role in glucose homeostasis
            through the timely release of the insulin hormone.   3. Pancreatic β cell regeneration and stem
            In vitro proliferation of human PSC-derived islets remains   cell
            an effective therapy, and a deeper comprehension of
            regeneration mechanics holds the potential for significant   Diabetes mellitus, a prominent pancreatic disorder, arises
            advancements in diabetes care. Both T1D and T2D are   from metabolic dysfunction due to a lack of β-cells that
            characterized by decreased cell numbers and declined   produce insulin. Replenishing β-cell populations through


            Volume 3 Issue 2 (2024)                         3                               doi: 10.36922/gpd.2996
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