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热休克蛋白70与衰老

Hsp70 and aging.

作者信息

Heydari A R, Takahashi R, Gutsmann A, You S, Richardson A

机构信息

Geriatric Research, Education and Clinical Center, Audie L., Murphy Memorial Veterans Hospital, San Antonio, Texas.

出版信息

Experientia. 1994 Nov 30;50(11-12):1092-8. doi: 10.1007/BF01923466.

DOI:10.1007/BF01923466
PMID:7988669
Abstract

An alteration in the ability of cells to express heat shock proteins could be physiologically important in aging because all living organisms show a reduced ability to respond to stress with increasing age. Using hepatocytes freshly isolated from young adult and old rats, we have shown that the induction of hsp70 expression by heat shock is reduced approximately 50% with age. The decrease in hsp70 expression occurs at the level of transcription and appears to arise from a defect in the heat shock transcription factor. Other investigators have also shown that the induction of hsp70 expression by heat shock as well as other stresses declines significantly with age in a variety of tissues from rats as well as mononuclear cells from human subjects. In addition, a decrease in the inducibility of hsp70 is observed with cell senescence in cultured cells. Therefore, it appears that a reduced ability to express hsp70 in response to stress may be a common phenomenon underlying the aging process.

摘要

细胞表达热休克蛋白能力的改变在衰老过程中可能具有重要的生理意义,因为所有生物随着年龄增长对压力的反应能力都会下降。我们使用从年轻成年大鼠和老年大鼠新鲜分离的肝细胞,发现热休克诱导的hsp70表达随年龄增长降低了约50%。hsp70表达的降低发生在转录水平,似乎是由热休克转录因子的缺陷引起的。其他研究人员也表明,热休克以及其他应激诱导的hsp70表达在大鼠的各种组织以及人类受试者的单核细胞中均随年龄显著下降。此外,在培养细胞中,随着细胞衰老,hsp70的诱导性也会降低。因此,似乎应激时表达hsp70的能力降低可能是衰老过程的一个普遍现象。

相似文献

1
Hsp70 and aging.热休克蛋白70与衰老
Experientia. 1994 Nov 30;50(11-12):1092-8. doi: 10.1007/BF01923466.
2
The expression of heat shock protein 70 decreases with age in lymphocytes from rats and rhesus monkeys.大鼠和恒河猴淋巴细胞中热休克蛋白70的表达随年龄增长而降低。
Exp Cell Res. 1995 May;218(1):310-8. doi: 10.1006/excr.1995.1160.
3
Effect of caloric restriction on the expression of heat shock protein 70 and the activation of heat shock transcription factor 1.热量限制对热休克蛋白70表达及热休克转录因子1激活的影响。
Dev Genet. 1996;18(2):114-24. doi: 10.1002/(SICI)1520-6408(1996)18:2<114::AID-DVG4>3.0.CO;2-C.
4
Expression of heat shock protein 70 is altered by age and diet at the level of transcription.热休克蛋白70的表达在转录水平上会因年龄和饮食而发生改变。
Mol Cell Biol. 1993 May;13(5):2909-18. doi: 10.1128/mcb.13.5.2909-2918.1993.
5
Expression of heat shock protein 70 decreases with age in hepatocytes and splenocytes from female rats.雌性大鼠肝细胞和脾细胞中热休克蛋白70的表达随年龄增长而降低。
Mech Ageing Dev. 1999 Mar 15;107(3):255-70. doi: 10.1016/s0047-6374(98)00132-8.
6
Age-related alterations in the activation of heat shock transcription factor 1 in rat hepatocytes.大鼠肝细胞中热休克转录因子1激活的年龄相关变化。
Exp Cell Res. 2000 Apr 10;256(1):83-93. doi: 10.1006/excr.2000.4808.
7
Effect of age and dietary restriction on expression of heat shock protein 70 in rat alveolar macrophages.年龄和饮食限制对大鼠肺泡巨噬细胞中热休克蛋白70表达的影响。
Mech Ageing Dev. 1998 Aug 1;104(1):59-73. doi: 10.1016/s0047-6374(98)00052-9.
8
The expression of heat shock protein 70 decreases with cellular senescence in vitro and in cells derived from young and old human subjects.在体外以及来自年轻和老年人类受试者的细胞中,热休克蛋白70的表达随细胞衰老而降低。
Exp Cell Res. 1998 Jun 15;241(2):404-13. doi: 10.1006/excr.1998.4069.
9
Heat induced expression of CD95 and its correlation with the activation of apoptosis upon heat shock in rat histiocytic tumor cells.热诱导大鼠组织细胞瘤细胞中CD95的表达及其与热休克时细胞凋亡激活的相关性。
FEBS Lett. 2000 Apr 28;472(2-3):271-5. doi: 10.1016/s0014-5793(00)01467-8.
10
Hsp70 accumulation in chondrocytic cells exposed to high continuous hydrostatic pressure coincides with mRNA stabilization rather than transcriptional activation.暴露于持续高静水压力下的软骨细胞中热休克蛋白70(Hsp70)的积累与信使核糖核酸(mRNA)的稳定有关,而非转录激活。
Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2319-24. doi: 10.1073/pnas.95.5.2319.

引用本文的文献

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Proteins with cognition-associated structural changes in a rat model of aging exhibit reduced refolding capacity.在衰老大鼠模型中具有认知相关结构变化的蛋白质表现出降低的重折叠能力。
Sci Adv. 2025 Jul 11;11(28):eadt3778. doi: 10.1126/sciadv.adt3778.
2
Hsp70: A Multifunctional Chaperone in Maintaining Proteostasis and Its Implications in Human Disease.热休克蛋白70:维持蛋白质稳态的多功能伴侣蛋白及其在人类疾病中的意义
Cells. 2025 Mar 29;14(7):509. doi: 10.3390/cells14070509.
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Cognition-Associated Protein Structural Changes in a Rat Model of Aging are Related to Reduced Refolding Capacity.

本文引用的文献

1
The effect of age on the synthesis of two heat shock proteins in the hsp70 family.年龄对热休克蛋白70家族中两种热休克蛋白合成的影响。
J Gerontol. 1993 Mar;48(2):B50-6. doi: 10.1093/geronj/48.2.b50.
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Activation of human heat shock genes is accompanied by oligomerization, modification, and rapid translocation of heat shock transcription factor HSF1.人类热休克基因的激活伴随着热休克转录因子HSF1的寡聚化、修饰及快速易位。
Mol Cell Biol. 1993 Apr;13(4):2486-96. doi: 10.1128/mcb.13.4.2486-2496.1993.
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Cells in stress: transcriptional activation of heat shock genes.
衰老大鼠模型中与认知相关的蛋白质结构变化与重折叠能力降低有关。
bioRxiv. 2024 Sep 24:2024.09.20.614172. doi: 10.1101/2024.09.20.614172.
4
Heat Shock Protein 70 Constitutes a Promising Novel Biomarker in Differential Diagnosis between Takotsubo Syndrome and Non-ST-Segment Elevation Myocardial Infarction.热休克蛋白70是鉴别应激性心肌病和非ST段抬高型心肌梗死的一种有前景的新型生物标志物。
J Clin Med. 2024 Jul 16;13(14):4152. doi: 10.3390/jcm13144152.
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The role of melatonin deficiency induced by pinealectomy on motor activity and anxiety responses in young adult, middle-aged and old rats.松果体切除导致褪黑素缺乏对年轻成年、中年和老年大鼠运动活动和焦虑反应的作用。
Behav Brain Funct. 2024 Feb 27;20(1):3. doi: 10.1186/s12993-024-00229-y.
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Molecular Chaperones as Therapeutic Target: Hallmark of Neurodegenerative Disorders.分子伴侣作为治疗靶点:神经退行性疾病的标志。
Mol Neurobiol. 2024 Jul;61(7):4750-4767. doi: 10.1007/s12035-023-03846-2. Epub 2023 Dec 21.
7
Interactions of amyloidogenic proteins with mitochondrial protein import machinery in aging-related neurodegenerative diseases.衰老相关神经退行性疾病中淀粉样蛋白与线粒体蛋白导入机制的相互作用。
Front Physiol. 2023 Nov 2;14:1263420. doi: 10.3389/fphys.2023.1263420. eCollection 2023.
8
Closest horizons of Hsp70 engagement to manage neurodegeneration.用于管理神经退行性变的Hsp70结合的最接近范围。
Front Mol Neurosci. 2023 Sep 19;16:1230436. doi: 10.3389/fnmol.2023.1230436. eCollection 2023.
9
Vegetable Oil-Peroxidation Product 'Hydroxynonenal' Causes Hepatocyte Injury and Steatosis via Hsp70.1 and BHMT Disorders in the Monkey Liver.植物油过氧化物产物“4-羟基壬烯醛”通过猴肝中热休克蛋白 70.1 和 BHMT 紊乱引起肝细胞损伤和脂肪变性。
Nutrients. 2023 Apr 14;15(8):1904. doi: 10.3390/nu15081904.
10
Mitochondrial HSP70 Chaperone System-The Influence of Post-Translational Modifications and Involvement in Human Diseases.线粒体 HSP70 伴侣系统-翻译后修饰的影响及其在人类疾病中的作用。
Int J Mol Sci. 2021 Jul 28;22(15):8077. doi: 10.3390/ijms22158077.
应激状态下的细胞:热休克基因的转录激活
Science. 1993 Mar 5;259(5100):1409-10. doi: 10.1126/science.8451637.
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Activation of heat shock gene transcription by heat shock factor 1 involves oligomerization, acquisition of DNA-binding activity, and nuclear localization and can occur in the absence of stress.热休克因子1对热休克基因转录的激活涉及寡聚化、获得DNA结合活性以及核定位,并且在无应激条件下也可发生。
Mol Cell Biol. 1993 Mar;13(3):1392-407. doi: 10.1128/mcb.13.3.1392-1407.1993.
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Protein traffic on the heat shock promoter: parking, stalling, and trucking along.热休克启动子上的蛋白质转运:驻留、停滞与持续前行。
Cell. 1993 Jul 16;74(1):1-4. doi: 10.1016/0092-8674(93)90286-y.
6
Stress response of senescent T lymphocytes: reduced hsp70 is independent of the proliferative block.衰老T淋巴细胞的应激反应:热休克蛋白70降低与增殖阻滞无关。
J Gerontol. 1994 Mar;49(2):B65-70. doi: 10.1093/geronj/49.2.b65.
7
Vascular heat shock protein expression in response to stress. Endocrine and autonomic regulation of this age-dependent response.血管热休克蛋白对应激的表达。这种年龄依赖性反应的内分泌和自主调节。
J Clin Invest. 1993 Feb;91(2):465-73. doi: 10.1172/JCI116224.
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Expression of heat shock protein 70 is altered by age and diet at the level of transcription.热休克蛋白70的表达在转录水平上会因年龄和饮食而发生改变。
Mol Cell Biol. 1993 May;13(5):2909-18. doi: 10.1128/mcb.13.5.2909-2918.1993.
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Risk factors for heatstroke. A case-control study.中暑的危险因素。一项病例对照研究。
JAMA. 1982 Jun 25;247(24):3332-6.
10
Morbidity and mortality associated with the July 1980 heat wave in St Louis and Kansas City, Mo.1980年7月密苏里州圣路易斯市和堪萨斯城热浪相关的发病率和死亡率
JAMA. 1982 Jun 25;247(24):3327-31.