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Localization of Heat Shock Proteins ...

Deane, Catherine.

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Localization of Heat Shock Proteins HSPA6 (Hsp70B'), HSPA1A (Hsp70-1) and HSPA8 (Hsc70) in Cultured Human Neuronal Cells.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Localization of Heat Shock Proteins HSPA6 (Hsp70B'), HSPA1A (Hsp70-1) and HSPA8 (Hsc70) in Cultured Human Neuronal Cells./
作者:	Deane, Catherine.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2019,
面頁冊數:	212 p.
附註:	Source: Dissertations Abstracts International, Volume: 81-04, Section: B.
Contained By:	Dissertations Abstracts International81-04B.
標題:	Cellular biology. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=13428544
ISBN:	9781088325353

Localization of Heat Shock Proteins HSPA6 (Hsp70B'), HSPA1A (Hsp70-1) and HSPA8 (Hsc70) in Cultured Human Neuronal Cells.
Deane, Catherine.

Localization of Heat Shock Proteins HSPA6 (Hsp70B'), HSPA1A (Hsp70-1) and HSPA8 (Hsc70) in Cultured Human Neuronal Cells. - Ann Arbor : ProQuest Dissertations & Theses, 2019 - 212 p.

Source: Dissertations Abstracts International, Volume: 81-04, Section: B.

Thesis (Ph.D.)--University of Toronto (Canada), 2019.

This item must not be sold to any third party vendors.

Heat shock proteins (Hsps) are protein repair agents that detect and refold misfolded proteins and prevent their aggregation. Accumulation of protein aggregates is a key feature of neurodegenerative diseases. Treatments that showed beneficial effects in current animal models of neurodegenerative diseases have repeatedly failed in human clinical trials. A better understanding of the proteostasis machinery in human cells is required to design more effective therapeutic compounds. HSPA6 (Hsp70B') is a stress-inducible member of the HSPA (Hsp70) multigene family that is absent in rat and mouse genomes and has been little studied compared to inducible HSPA1A (Hsp70-1), or constitutively expressed HSPA8 (Hsc70). HSPAs are involved in refolding proteins that misfold due to stress or disease. Binding to DNAJ (Hsp40) inhibits aggregation of misfolded proteins until they can be refolded by HSPA, but this machine cannot dissociate aggregated proteins. Recent studies have identified a disaggregase function performed by the mammalian HSPH (Hsp110) family in co-operation with HSPA/DNAJ in vitro. To advance knowledge of the mammalian disaggregation/refolding machine, this thesis investigates localization of HSPA6, HSPA1A, and HSPA8 with other components of the machine following stress in differentiated human neuronal SH-SY5Y cells. Unique targeting of HSPA6 to nuclear perispeckles and differential localization with disaggregation/refolding machine components at the nucleolus compared to HSPA1A or HSPA8 is observed following thermal stress. siRNA knockdown demonstrates that HSPA6 is protective in the neuronal stress response. MG132 proteotoxicity induces HSPA6 which targets the periphery of cytoplasmic protein aggregates with components of the disaggregation/refolding machine and thus may be involved in the response of differentiated neuronal cells to protein aggregation. Constitutively expressed HSPA8 exhibits similar intracellular targeting as inducible HSPA1A and may act as a rapid stress responder in neuronal cells, circumventing the time lag required to upregulate HSPA1A. In cancer cells, elevated levels of Hsps contribute to their ability to resist cell death. The chemotherapeutic agent cisplatin induces components of the disaggregation/refolding machine. Knockdown of HSPA family members enhances the killing effect of cisplatin on human neuroblastoma cells.

ISBN: 9781088325353Subjects--Topical Terms:

3172791
Cellular biology.
Subjects--Index Terms:

Differentiated SH-SY5Y human neuronal cells

Localization of Heat Shock Proteins HSPA6 (Hsp70B'), HSPA1A (Hsp70-1) and HSPA8 (Hsc70) in Cultured Human Neuronal Cells.
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520 $a Heat shock proteins (Hsps) are protein repair agents that detect and refold misfolded proteins and prevent their aggregation. Accumulation of protein aggregates is a key feature of neurodegenerative diseases. Treatments that showed beneficial effects in current animal models of neurodegenerative diseases have repeatedly failed in human clinical trials. A better understanding of the proteostasis machinery in human cells is required to design more effective therapeutic compounds. HSPA6 (Hsp70B') is a stress-inducible member of the HSPA (Hsp70) multigene family that is absent in rat and mouse genomes and has been little studied compared to inducible HSPA1A (Hsp70-1), or constitutively expressed HSPA8 (Hsc70). HSPAs are involved in refolding proteins that misfold due to stress or disease. Binding to DNAJ (Hsp40) inhibits aggregation of misfolded proteins until they can be refolded by HSPA, but this machine cannot dissociate aggregated proteins. Recent studies have identified a disaggregase function performed by the mammalian HSPH (Hsp110) family in co-operation with HSPA/DNAJ in vitro. To advance knowledge of the mammalian disaggregation/refolding machine, this thesis investigates localization of HSPA6, HSPA1A, and HSPA8 with other components of the machine following stress in differentiated human neuronal SH-SY5Y cells. Unique targeting of HSPA6 to nuclear perispeckles and differential localization with disaggregation/refolding machine components at the nucleolus compared to HSPA1A or HSPA8 is observed following thermal stress. siRNA knockdown demonstrates that HSPA6 is protective in the neuronal stress response. MG132 proteotoxicity induces HSPA6 which targets the periphery of cytoplasmic protein aggregates with components of the disaggregation/refolding machine and thus may be involved in the response of differentiated neuronal cells to protein aggregation. Constitutively expressed HSPA8 exhibits similar intracellular targeting as inducible HSPA1A and may act as a rapid stress responder in neuronal cells, circumventing the time lag required to upregulate HSPA1A. In cancer cells, elevated levels of Hsps contribute to their ability to resist cell death. The chemotherapeutic agent cisplatin induces components of the disaggregation/refolding machine. Knockdown of HSPA family members enhances the killing effect of cisplatin on human neuroblastoma cells.
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