Endoplasmic reticulum stress and muscle dysfunction in congenital lipodystrophies

被引:7
作者
Araujo de Melo Campos, Julliane Tamara [1 ]
Dantas de Medeiros, Jorge Luiz [2 ,3 ]
Cardoso de Melo, Maria Eduarda [1 ]
Alvares da Silva, Monique [1 ]
de Sena, Matheus Oliveira [1 ]
Craveiro Sarmento, Aquiles Sales [4 ]
Agnez Lima, Lucymara Fassarella [1 ]
de Freitas Fregonezi, Guilherme Augusto [2 ,3 ,5 ]
Lima, Josivan Gomes [6 ]
机构
[1] Univ Fed Rio Grande do Norte, Ctr Biociencias, Dept Biol Celular & Genet, Lab Biol Mol & Genom, Natal, RN, Brazil
[2] Univ Fed Rio Grande do Norte, PneumoCardioVasc Lab HUOL, Hosp Univ Onofre Lopes, Empresa Brasileira Serv Hosp, Natal, RN, Brazil
[3] Univ Fed Rio Grande do Norte, Dept Fisioterapia, Natal, RN, Brazil
[4] UFS, Unidade Lab Anal Clin & Anat Patol, Hosp Univ Lagarto HUL, Lagarto, SE, Brazil
[5] Univ Fed Rio Grande do Norte, Dept Fisioterapia, Lab Inovacao Tecnol Reabilitacao, Natal, RN, Brazil
[6] Univ Fed Rio Grande do Norte, Hosp Univ Onofre Lopes HUOL, Dept Med Clin, Natal, RN, Brazil
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2021年 / 1867卷 / 06期
关键词
Inherited lipodystrophies; ER stress; Muscle dysfunctions; UNFOLDED PROTEIN RESPONSE; FAMILIAL PARTIAL LIPODYSTROPHY; ER-STRESS; GENERALIZED LIPODYSTROPHY; OXIDATIVE STRESS; SKELETAL-MUSCLE; LAMIN A/C; NUCLEAR LAMINS; LIPID-METABOLISM; DOWN-REGULATION;
D O I
10.1016/j.bbadis.2021.166120
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
Lipodystrophy syndromes are a group of rare diseases related to the pathological impairment of adipose tissue and metabolic comorbidities, including dyslipidemia, diabetes, insulin resistance, hypoleptinemia, and hypoadiponectinemia. They can be categorized as partial or generalized according to the degree of fat loss, and inherited or acquired disorders, if they are associated with genetic mutations or are related to autoimmunity, respectively. Some types of lipodystrophies have been associated with changes in both redox and endoplasmic reticulum (ER) homeostasis as well as muscle dysfunction (MD). Although ER stress (ERS) has been related to muscle dysfunction (MD) in many diseases, there is no data concerning its role in lipodystrophies' muscle physiopathology. Here we focused on congenital lipodystrophies associated with ERS and MD. We also described recent advances in our understanding of the relationships among ERS, MD, and genetic lipodystrophies, highlighting the adiponectin-protective roles.
引用
收藏
页数:19
相关论文
共 195 条
[1]   Pathogenesis of Insulin Resistance in Skeletal Muscle [J].
Abdul-Ghani, Muhammad A. ;
DeFronzo, Ralph A. .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2010,
[2]   Structure and Molecular Mechanism of ER Stress Signaling by the Unfolded Protein Response Signal Activator IRE1 [J].
Adams, Christopher J. ;
Kopp, Megan C. ;
Larburu, Natacha ;
Nowak, Piotr R. ;
Ali, Maruf M. U. .
FRONTIERS IN MOLECULAR BIOSCIENCES, 2019, 6
[3]   ER stress in skeletal muscle remodeling and myopathies [J].
Afroze, Dil ;
Kumar, Ashok .
FEBS JOURNAL, 2019, 286 (02) :379-398
[4]   AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34 [J].
Agarwal, AK ;
Arioglu, E ;
de Almeida, S ;
Akkoc, N ;
Taylor, SI ;
Bowcock, AM ;
Barnes, RI ;
Garg, A .
NATURE GENETICS, 2002, 31 (01) :21-23
[5]   Clinical spectra of neuromuscular manifestations in patients with lipodystrophy: A multicenter study [J].
Akinci, Gulcin ;
Topaloglu, Haluk ;
Demir, Tevfik ;
Danyeli, Ayca Ersen ;
Talim, Beril ;
Keskin, Fatma Ela ;
Kadioglu, Pinar ;
Talip, Enez ;
Altay, Canan ;
Yaylali, Guzin Fidan ;
Bilen, Habib ;
Nur, Banu ;
Demir, Leyla ;
Onay, Huseyin ;
Akinci, Baris .
NEUROMUSCULAR DISORDERS, 2017, 27 (10) :923-930
[6]   Higher Adiponectin Levels in Patients with Berardinelli-Seip Congenital Lipodystrophy due to Seipin as compared with 1-Acylglycerol-3-Phosphate-O-Acyltransferase-2 Deficiency [J].
Antuna-Puente, Barbara ;
Boutet, Emilie ;
Vigouroux, Corinne ;
Lascols, Olivier ;
Slama, Laurence ;
Caron-Debarle, Martine ;
Khallouf, Eliane ;
Levy-Marchal, Claire ;
Capeau, Jacqueline ;
Bastard, Jean-Philippe ;
Magre, Jocelyne .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2010, 95 (03) :1463-1468
[7]   Evaluation of Oxidative Stress Markers and their Correlation with Respiratory Muscle Strength in Congenital Generalized Lipodystrophy [J].
Araujo de Melo Campos, Julliane Tamara ;
Craveiro Sarmento, Aquiles Sales ;
Dantas De Medeiros, Jorge Luiz ;
Bezerra, Bruno Carneiro ;
Xavier Nobre, Thaiza Teixeira ;
Gualdi, Lucien Peroni ;
Agnez Lima, Lucymara Fassarella ;
Lima, Josivan Gomes .
EUROPEAN RESPIRATORY JOURNAL, 2019, 54
[8]   Diagnosis and treatment of lipodystrophy: a step-by-step approach [J].
Araujo-Vilar, D. ;
Santini, F. .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2019, 42 (01) :61-73
[9]   Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy [J].
Ardissone, Anna ;
Bragato, Cinzia ;
Caffi, Lorella ;
Blasevich, Flavia ;
Maestrini, Sabrina ;
Bianchi, Maria Luisa ;
Morandi, Lucia ;
Moroni, Isabella ;
Mora, Marina .
BMC MEDICAL GENETICS, 2013, 14
[10]   Peroxisome Proliferator-Activated Receptor-γ Mutations Responsible for Lipodystrophy With Severe Hypertension Activate the Cellular Renin-Angiotensin System [J].
Auclair, Martine ;
Vigouroux, Corinne ;
Boccara, Franck ;
Capel, Emilie ;
Vigeral, Catherine ;
Guerci, Bruno ;
Lascols, Olivier ;
Capeau, Jacqueline ;
Caron-Debarle, Martine .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2013, 33 (04) :829-U449