468076 NANOG Rejuvenates the Impaired Extracellular Matrix Expression in Senescent Cells and Thus Restores the Decreased Mechanical Properties of Engineered Tissues

Monday, November 14, 2016
Grand Ballroom B (Hilton San Francisco Union Square)
Na Rong1, Panagiotis Mistriotis2, Xiaoyan Wang3, Georgios Tseropoulos3 and Stelios T. Andreadis4, (1)Chemical & Biological Engineering, University at Buffalo, Buffalo, NY, (2)Chemical and Biological Engineering, University at Buffalo, The State University of New York, Buffalo, NY, (3)Chemical and Biological Engineering, University at Buffalo, Buffalo, NY, (4)Department of Chemical and Biological Engineering, University at Buffalo, Buffalo, NY

Extracellular matrix molecules (ECM) such as elastin and collagen are critical in regulating the arterial mechanical properties. Elastin, imparts the elastic properties to the vascular wall whereas collagen regulates the strength of tissues in general and the arterial wall in particular. Notably, aging is accompanied by significant reduction in the elastic properties of the vascular wall mostly due to loss of elastin fibers. Similarly, although crosslinking of old collagen increases, new collagen production decreases with aging. As a result, aging is characterized by stiffer vessels, which are prone to aneurysms. Hence, there is a need to develop strategies to restore the impaired deposition of ECM. Here we report that ectopic expression of the pluripotent factor, NANOG, in aged myogenic progenitors could restore the impaired ECM production and increase the mechanical properties of aged engineered tissues.

To study the effect of NANOG on aged cells, we applied two widely established models of aging i.e. replicative senescence of human Mesenchymal Stem Cells (MSC), and myofibroblasts derived from Hutchinson’s Guilford Progeria Syndrome (HGPS) patients. Human Mesenchymal Stem Cells (MSC) were induced to senescence by serially passaging. To express NANOG, cells were transduced with a tetracycline-inducible virus, which allowed expression of NANOG only in the presence of Doxycycline (Dox). Upon senescence, cells were treated with DOX (LPN) and the production of ECM was evaluated and compared to Early passage (EP) and senescent cells (Late Passage or LP). Similar experiments were also performed with HGPS derived cells.

Our results show that senescence reduced the production of both Collagen 3 and Elastin. In agreement, tissues engineered using senescent cells showed inferior mechanical properties. Interestingly, NANOG restored the capacity of senescent cells to express ECM molecules and increased the mechanical properties of engineered tissues. Next we performed RNA-seq to identify the mechanism mediating the effects of NANOG on ECM production. We found that NANOG altered the expression of genes that are part of the TGFbeta pathway, which is known to be necessary in ECM production. In agreement, we discovered that NANOG restored the activity of the TGFbeta pathway that was impaired in senescent cells, whereas inhibition of the TGFbeta pathway with either shRNA (SMAD2, SMAD3, SMAD4) or chemical inhibitor (SB431542) abolished the effects of NANOG. Conversely, overexpression of SMAD2 and SMAD3 increased ECM production.

In conclusion, our study provides a novel strategy to restore the impaired production of ECM, which may have broad applications in tissue regeneration and anti-aging treatments.

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