Research Progress in Clearance of Senescent Cells in Aging and Age-related Diseases

被引:0
作者
Chen Xiang-Ning [1 ]
Liu Yang [2 ,3 ]
Ji Jun-Feng [1 ,4 ]
机构
[1] Zhejiang Univ, Sch Med, Stem Cell & Regenerat Med Res Ctr, Hangzhou 310058, Zhejiang, Peoples R China
[2] Henan Univ, Sch Pharm, Henan Macquarie Univ Joint Ctr Biomed Innovat, Kaifeng 475001, Peoples R China
[3] Macquarie Univ, Fac Med & Hlth Sci, Dept Biomed Sci, Sydney, NSW, Australia
[4] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Bone Marrow Transplantat Ctr, Hangzhou 310003, Zhejiang, Peoples R China
关键词
cellular senescence; anti-aging; age-related disease; drug target; CELLULAR SENESCENCE; CHONDROCYTE SENESCENCE; PIGMENT ACCUMULATION; STEM-CELLS; IN-VIVO; OSTEOARTHRITIS; APOPTOSIS; GROWTH; LIFE; TRANSPLANTATION;
D O I
10.16476/j.pibb.2019.0194
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aging is an emerging and important research area. With the accumulation of knowledge in related fields and the advancement of technology, people gradually realized that aging itself can be intervened and it is of great scientific and practical significance to delay aging, especially delaying the occurrence and development of age-related diseases. Among the many factors that cause individual aging, the accumulation of senescent cells is considered to be an important reason that leads to organ aging and degeneration, and finally causes the age-related diseases. In recent years, a number of studies have shown that removing senescent cells in vivo can delay the occurrence of multiple age-related diseases, which directly proves that senescent cells are one of the important causes of age-related diseases, providing a new target for the treatment of age-related diseases. Cellular senescence is generally considered due to the activation of cell cycle inhibition pathway induced by accumulation of damages, and the cells permanently exit the proliferation cycle. Senescent cells undergo changes in cell morphology, transcriptional profiles, protein homeostasis, epigenome and metabolism. Moreover, senescent cells resist apoptosis and therefore accumulate in multiple organs and tissues in the body. Senescent cells secrete a number of inflammatory factors, leading to a local non-infectious inflammatory tissue microenvironment, which will cause organ function deterioration and a variety of age-related diseases. Therefore, several research groups have screened the library of small molecular compounds and found that certain compounds can selectively eliminate senescent cells by targeting pathways underpinning senescent cells' resistance to apoptosis. These small molecular compounds are called "senolytics ", denoting compounds for killing senescent cells. Senolytics have been shown to alleviate multiple age-related diseases and prolong the lifespan in animal models. Therefore, targeted killing of senescent cells has an important clinical application prospect for the treatment of a variety of age-related diseases so as to improve the healthy lifespan. In addition, strategies such as stem cell transplantation, gene editing and heterochronic parabiosis are also of great significance and inspiration in the development of anti aging research. By summarizing the recent important progress in the field of senescent cell clearance and a variety of anti-aging strategies, this paper briefly reviews the history of cellular senescence research, discusses the relationship between cellular senescence and age-related diseases, emphasizing on the potential therapeutic applications by targeting senescent cells and the limitations, as well as the further research directions in this field.
引用
收藏
页码:1150 / 1161
页数:12
相关论文
共 104 条
[81]   Systemic Regulation of the Age-Related Decline of Pancreatic β-Cell Replication [J].
Salpeter, Seth J. ;
Khalaileh, Abed ;
Weinberg-Corem, Noa ;
Ziv, Oren ;
Glaser, Benjamin ;
Dor, Yuval .
DIABETES, 2013, 62 (08) :2843-2848
[82]   Cellular Senescence in Postmitotic Cells: Beyond Growth Arrest [J].
Sapieha, Przemyslaw ;
Mallette, Frederick A. .
TRENDS IN CELL BIOLOGY, 2018, 28 (08) :595-607
[83]   Cellular senescence mediates fibrotic pulmonary disease [J].
Schafer, Marissa J. ;
White, Thomas A. ;
Iijima, Koji ;
Haak, Andrew J. ;
Ligresti, Giovanni ;
Atkinson, Elizabeth J. ;
Oberg, Ann L. ;
Birch, Jodie ;
Salmonowicz, Hanna ;
Zhu, Yi ;
Mazula, Daniel L. ;
Brooks, Robert W. ;
Fuhrmann-Stroissnigg, Heike ;
Pirtskhalava, Tamar ;
Prakash, Y. S. ;
Tchkonia, Tamara ;
Robbins, Paul D. ;
Aubry, Marie Christine ;
Passos, Joao F. ;
Kirkland, James L. ;
Tschumperlin, Daniel J. ;
Kita, Hirohito ;
LeBrasseur, Nathan K. .
NATURE COMMUNICATIONS, 2017, 8
[84]   Forging a signature of in vivo senescence [J].
Sharpless, Norman E. ;
Sherr, Charles J. .
NATURE REVIEWS CANCER, 2015, 15 (07) :397-408
[85]   Innate immunosenescence: Effect of aging on cells and receptors of the innate immune system in humans [J].
Solana, Rafael ;
Tarazona, Raquel ;
Gayoso, Inmaculada ;
Lesur, Olivier ;
Dupuis, Gilles ;
Fulop, Tamas .
SEMINARS IN IMMUNOLOGY, 2012, 24 (05) :331-341
[86]   Senescence Is a Developmental Mechanism that Contributes to Embryonic Growth and Patterning [J].
Storer, Mekayla ;
Mas, Alba ;
Robert-Moreno, Alexandre ;
Pecoraro, Matteo ;
Ortells, M. Carmen ;
Di Giacomo, Valeria ;
Yosef, Reut ;
Pilpel, Noam ;
Krizhanovsky, Valery ;
Sharpe, James ;
Keyes, William M. .
CELL, 2013, 155 (05) :1119-1130
[87]   RATE AND MAGNITUDE OF AGE PIGMENT ACCUMULATION IN THE HUMAN MYOCARDIUM [J].
STREHLER, BL ;
MARK, DD ;
MILDVAN, AS ;
GEE, MV .
JOURNALS OF GERONTOLOGY, 1959, 14 (04) :430-439
[88]   Advances in stem-cell-generated transplantation therapy for Parkinson's disease [J].
Sundberg, Maria ;
Isacson, Ole .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2014, 14 (04) :437-453
[89]   Cellular senescence and the senescent secretory phenotype: therapeutic opportunities [J].
Tchkonia, Tamara ;
Zhu, Yi ;
van Deursen, Jan ;
Campisi, Judith ;
Kirkland, James L. .
JOURNAL OF CLINICAL INVESTIGATION, 2013, 123 (03) :966-972
[90]   Targeted Elimination of Senescent Beta Cells Prevents Type 1 Diabetes [J].
Thompson, Peter J. ;
Shah, Ajit ;
Ntranos, Vasilis ;
Van Gool, Frederic ;
Atkinson, Mark ;
Bhushan, Anil .
CELL METABOLISM, 2019, 29 (05) :1045-+