Literature DB >> 16399914

Use of telomerase to create bioengineered tissues.

Jerry W Shay1, Woodring E Wright.   

Abstract

Telomeres are repetitive DNA (TTAGGG) elements at the ends of chromosomes. Telomerase is a ribonucleoprotein complex that catalyzes the addition of telomeric sequences to the ends of chromosomes. The catalytic protein component of telomerase (hTERT) is expressed only in specific germ line cells, proliferative stem cells of renewal tissues, and cancer cells. The expression of hTERT in normal cells reconstitutes telomerase activity and circumvents the induction of senescence. Telomeres shorten with each cell division, eventually leading to senescence (aging), due to incomplete lagging DNA strand synthesis and end-processing events, and because telomerase activity is not detected in most somatic tissues. There are specific tissues and locations in which replicative senescence likely contributes to the decline in human physiological function with increased age and with chronic illnesses. While expressing hTERT in cells results in the maintenance of telomere length and greatly extended life span, blocking replicative aging systemically would be predicted to increase the potential for tumor formation. However, there are many situations in which the transient rejuvenation of cells could be beneficial. Ectopic expression of hTERT has been shown to immortalize human skin keratinocytes, dermal fibroblasts, muscle satellite (stem), and vascular endothelial, myometrial, retinal-pigmented, and breast epithelial cells. In addition, human bronchial, corneal and skin cells expressing hTERT can be used to form organotypic (3D) cultures (bioengineered tissues) that express differentiation-specific proteins, demonstrating that hTERT by itself does not alter normal physiology. The production of hTERT-engineered tissues offers the possibility of producing tissues to treat a variety of chronic diseases and age-related medical conditions that are due to telomere-based replicative senescence.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16399914     DOI: 10.1196/annals.1356.037

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  17 in total

1.  Separation of telomerase functions by reverse genetics.

Authors:  Shibani Mukherjee; Eduardo J Firpo; Yang Wang; James M Roberts
Journal:  Proc Natl Acad Sci U S A       Date:  2011-09-26       Impact factor: 11.205

2.  Enhanced migration and CXCR4 over-expression in fibroblasts with telomerase reconstitution.

Authors:  Yi Qu; Meng Mao; Xihong Li; Lin Zhang; Xiang Huang; Chunlei Yang; Fengyang Zhao; Ying Xiong; Dezhi Mu
Journal:  Mol Cell Biochem       Date:  2008-03-25       Impact factor: 3.396

3.  Comparative analysis of myometrial and vascular smooth muscle cells to determine optimal cells for use in drug discovery.

Authors:  Shajila Siricilla; Kelsi M Knapp; Jackson H Rogers; Courtney Berger; Elaine L Shelton; Dehui Mi; Paige Vinson; Jennifer Condon; Bibhash C Paria; Jeff Reese; Quanhu Sheng; Jennifer L Herington
Journal:  Pharmacol Res       Date:  2019-05-09       Impact factor: 7.658

4.  Differentiation rather than aging of muscle stem cells abolishes their telomerase activity.

Authors:  Matthew S O'Connor; Morgan E Carlson; Irina M Conboy
Journal:  Biotechnol Prog       Date:  2009 Jul-Aug

Review 5.  Recent insights into the molecular mechanisms involved in aging and the malignant transformation of adult stem/progenitor cells and their therapeutic implications.

Authors:  Murielle Mimeault; Surinder K Batra
Journal:  Ageing Res Rev       Date:  2008-12-09       Impact factor: 10.895

Review 6.  Paracrine mechanisms in adult stem cell signaling and therapy.

Authors:  Massimiliano Gnecchi; Zhiping Zhang; Aiguo Ni; Victor J Dzau
Journal:  Circ Res       Date:  2008-11-21       Impact factor: 17.367

7.  Characterization of cellular senescence mechanisms in human corneal endothelial cells.

Authors:  Angela N Sheerin; S Kaye Smith; Katrin Jennert-Burston; Amy J Brook; Marcus C Allen; Badr Ibrahim; Dawn Jones; Corrin Wallis; Katrin Engelmann; William Rhys-Williams; Richard G A Faragher; David Kipling
Journal:  Aging Cell       Date:  2011-12-29       Impact factor: 9.304

8.  Accelerated cellular senescence in degenerate intervertebral discs: a possible role in the pathogenesis of intervertebral disc degeneration.

Authors:  Christine Lyn Le Maitre; Anthony John Freemont; Judith Alison Hoyland
Journal:  Arthritis Res Ther       Date:  2007       Impact factor: 5.156

9.  H-ras expression in immortalized keratinocytes produces an invasive epithelium in cultured skin equivalents.

Authors:  Melville B Vaughan; Ruben D Ramirez; Capri M Andrews; Woodring E Wright; Jerry W Shay
Journal:  PLoS One       Date:  2009-11-19       Impact factor: 3.240

Review 10.  Recent advances on skin-resident stem/progenitor cell functions in skin regeneration, aging and cancers and novel anti-aging and cancer therapies.

Authors:  Murielle Mimeault; Surinder K Batra
Journal:  J Cell Mol Med       Date:  2009-09-01       Impact factor: 5.310

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.