Cunningham Timothy J, Greenstein Jeffrey I, Loewenstern Joshua, Degermentzidis Elias, Yao Lihua
1 Department of Neurobiology and Anatomy, Drexel University College of Medicine , Philadelphia, Pennsylvania.
Rejuvenation Res. 2015 Apr;18(2):136-44. doi: 10.1089/rej.2014.1620.
Reducing the levels of toxic protein aggregates has become a focus of therapy for disorders like Alzheimer's and Parkinson's diseases, as well as for the general deterioration of cells and tissues during aging. One approach has been an attempt to influence the production or activity of a class of reparative chaperones called heat shock proteins (HSPs), of which HSP70 is a promising candidate. Manipulation of HSP70 expression results in disposal of misfolded protein aggregates that accumulate in aging and disease models. Recently, HSP70 has been shown to bind specifically to an amino-terminal sequence of a human diffusible survival evasion peptide (DSEP), dermcidin. This sequence includes CHEC-9, an orally available anti-inflammatory and cell survival peptide. In the present study, we found that the CHEC-9 peptide also binds HSP70 in the cytosol of the cerebral cortex after oral delivery in normal rats. Western analysis of non-heat-denatured, unreduced samples suggested that peptide treatment increased the level of active HSP70 monomers from the pool of chaperone oligomers, a process that may be stimulated by potentiation of the chaperone's adenosine triphosphatase (ATPase). In these samples, a small but consistent gel shift was observed for glyceraldehyde 3-phosphate dehydrogenase (GAPDH), a multifunctional protein whose aggregation is influenced by HSP70. CHEC-9 treatment of an in vitro model of α-synuclein aggregation also results in HSP70-dependent dissolution of these aggregates. HSP70 oligomer-monomer equilibrium and its potential to control protein aggregate disease warrant increased experimental attention, especially if a peptide fragment of an endogenous human protein can influence the process.
降低有毒蛋白质聚集体的水平已成为治疗阿尔茨海默病和帕金森病等疾病以及衰老过程中细胞和组织普遍退化的重点。一种方法是试图影响一类称为热休克蛋白(HSPs)的修复伴侣蛋白的产生或活性,其中HSP70是一个有前景的候选者。操纵HSP70的表达可导致在衰老和疾病模型中积累的错误折叠蛋白质聚集体的清除。最近,已证明HSP70能特异性结合人可扩散生存逃避肽(DSEP)——皮肤杀菌肽的氨基末端序列。该序列包括CHEC-9,一种口服可用的抗炎和细胞存活肽。在本研究中,我们发现正常大鼠口服给药后,CHEC-9肽也能在大脑皮质的细胞质中结合HSP70。对非热变性、未还原样品的蛋白质免疫印迹分析表明,肽处理可增加伴侣寡聚体池中活性HSP70单体的水平,这一过程可能受到伴侣蛋白的三磷酸腺苷酶(ATPase)增强的刺激。在这些样品中,观察到甘油醛-3-磷酸脱氢酶(GAPDH)有一个小但一致的凝胶迁移,GAPDH是一种多功能蛋白质,其聚集受HSP70影响。用CHEC-9处理α-突触核蛋白聚集的体外模型也会导致这些聚集体在HSP70依赖下溶解。HSP70寡聚体-单体平衡及其控制蛋白质聚集疾病的潜力值得更多的实验关注,特别是如果一种内源性人类蛋白质的肽片段能够影响这一过程的话。