The Protein Disulfide Isomerase Family: Key Players in Health and Disease

被引:156
作者
Benham, Adam M. [1 ]
机构
[1] Univ Durham, Sch Biol & Biomed Sci, Durham DH1 3LE, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
TRIGLYCERIDE TRANSFER PROTEIN; ENDOPLASMIC-RETICULUM; ADIPONECTIN SECRETION; ESTROGEN-RECEPTOR; CHAPERONE PROTEIN; CRYSTAL-STRUCTURE; COMPLEX; BINDING; IDENTIFICATION; FUSION;
D O I
10.1089/ars.2011.4439
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
Significance: Protein disulfide isomerase (PDI) and its homologs have essential roles in the oxidative folding and chaperone-mediated quality control of proteins in the secretory pathway. In this review, the importance of PDI in health and disease will be examined, using examples from the fields of lipid homeostasis, hemostasis, infectious disease, cancer, neurodegeneration, and infertility. Recent Advances: Recent structural studies, coupled with cell biological, biochemical, and clinical approaches, have demonstrated that PDI family proteins are involved in a wide range of physiological and disease processes. Critical Issues: Critical issues in the field include understanding how and why a PDI family member is involved in a given disease, and defining the physiological client specificity of the various PDI proteins when they are expressed in different tissues. Future Directions: Future directions are likely to include the development of new and more specific reagents to study and manipulate PDI family function. The development of conditional mouse models in concert with clinical data will help us to understand the in vivo function of the different PDIs at the organism level. Taken together with advances in structural biology and biochemical studies, this should help us to further understand and modify PDIs' functional interactions. Antioxid. Redox Signal. 16, 781-789.
引用
收藏
页码:781 / 789
页数:9
相关论文
共 80 条
  • [1] Anterior specification of embryonic ectoderm:: the role of the Xenopus cement gland-specific gene XAG-2
    Aberger, F
    Weidinger, G
    Grunz, H
    Richter, K
    [J]. MECHANISMS OF DEVELOPMENT, 1998, 72 (1-2) : 115 - 130
  • [2] Protein disulfide isomerase-P5, down-regulated in the final stage of boar epididymal sperm maturation, catalyzes disulfide formation to inhibit protein function in oxidative refolding of reduced denatured lysozyme
    Akama, Kuniko
    Horikoshi, Tomoe
    Sugiyama, Atsushi
    Nakahata, Satoko
    Akitsu, Aoi
    Niwa, Nobuyoshi
    Intoh, Atsushi
    Kakui, Yasutaka
    Sugaya, Michiko
    Takei, Kazuo
    Imaizumi, Noriaki
    Sato, Takaya
    Matsumoto, Rena
    Iwahashi, Hitoshi
    Kashiwabara, Shin-ichi
    Baba, Tadashi
    Nakamura, Megumi
    Toda, Tosifusa
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2010, 1804 (06): : 1272 - 1284
  • [3] Defining the domain boundaries of the human protein disulfide isomerases
    Alanen, HI
    Salo, KEH
    Pekkala, M
    Siekkinen, HM
    Pirneskoski, A
    Ruddock, LW
    [J]. ANTIOXIDANTS & REDOX SIGNALING, 2003, 5 (04) : 367 - 374
  • [4] ERp44, a novel endoplasmic reticulum folding assistant of the thioredoxin family
    Anelli, T
    Alessio, M
    Mezghrani, A
    Simmen, T
    Talamo, F
    Bachi, A
    Sitia, R
    [J]. EMBO JOURNAL, 2002, 21 (04) : 835 - 844
  • [5] Sequential steps and checkpoints in the early exocytic compartment during secretory IgM biogenesis
    Anelli, Tiziana
    Ceppi, Stefania
    Bergamelli, Leda
    Cortini, Margherita
    Masciarelli, Silvia
    Valetti, Caterina
    Sitia, Roberto
    [J]. EMBO JOURNAL, 2007, 26 (19) : 4177 - 4188
  • [6] RETRACTED: Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis (Retracted Article)
    Atkin, Julie D.
    Farg, Manal A.
    Walker, Adam K.
    McLean, Catriona
    Tomas, Doris
    Horne, Malcolm K.
    [J]. NEUROBIOLOGY OF DISEASE, 2008, 30 (03) : 400 - 407
  • [7] RETRACTED: Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1 (Retracted article. See vol. 292, pg. 12007, 2017)
    Atkin, Julie D.
    Farg, Manal A.
    Turner, Bradley J.
    Tomas, Doris
    Lysaght, Judith A.
    Nunan, Janelle
    Rembach, Alan
    Nagley, Phillip
    Beart, Philip M.
    Cheema, Surindar S.
    Horne, Malcolm K.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (40) : 30152 - 30165
  • [8] ADAMs and protein disulfide isomerase: The key to regulated cell-surface protein ectodomain shedding?
    Bass, Rosemary
    Edwards, Dylan R.
    [J]. Biochemical Journal, 2010, 428 (03)
  • [9] Galectin-9 binding to cell surface protein disulfide isomerase regulates the redox environment to enhance T-cell migration and HIV entry
    Bi, Shuguang
    Hong, Patrick W.
    Lee, Benhur
    Baum, Linda G.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (26) : 10650 - 10655
  • [10] Cutting Edge: The Metalloproteinase ADAM17/TNF-α-Converting Enzyme Regulates Proteolytic Shedding of the MHC Class I-Related Chain B Protein
    Boutet, Philippe
    Agura-Gonzalez, Sonia
    Atkinson, Susan
    Pennington, Caroline J.
    Edwards, Dylan R.
    Murphy, Gillian
    Reyburn, Hugh T.
    Vales-Gomez, Mar
    [J]. JOURNAL OF IMMUNOLOGY, 2009, 182 (01) : 49 - 53