Targeting defective proteostasis in the collagenopathies

被引:23
作者
Wong, Madeline Y. [1 ]
Shoulders, Matthew D. [1 ]
机构
[1] MIT, Dept Chem, 77 Massachusetts Ave, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
OSTEOGENESIS IMPERFECTA PATIENTS; ENDOPLASMIC-RETICULUM; SELECTIVE-INHIBITION; MOLECULAR CHAPERONE; MUTANT COLLAGEN; STRESS-RESPONSE; MOUSE MODEL; MUTATIONS; ACTIVATION; GROWTH;
D O I
10.1016/j.cbpa.2019.02.021
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
The collagenopathies are a diverse group of diseases caused primarily by mutations in collagen genes. The resulting disruptions in collagen biogenesis can impair development, cause cellular dysfunction, and severely impact connective tissues. Most existing treatment options only address patient symptoms. Yet, while the disease-causing genes and proteins themselves are difficult to target, increasing evidence suggests that resculpting the intracellular proteostasis network, meaning the machineries responsible for producing and ensuring the integrity of collagen, could provide substantial benefit. We present a proteostasis-focused perspective on the collagenopathies, emphasizing progress toward understanding how mechanisms of collagen proteostasis are disrupted in disease. In parallel, we highlight recent advances in small molecule approaches to tune endoplasmic reticulum proteostasis that may prove useful in these disorders.
引用
收藏
页码:80 / 88
页数:9
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