The Influence of Sex Hormones in Liver Function and Disease

被引:39
作者
Kasarinaite, Alvile [1 ]
Sinton, Matthew [2 ,3 ]
Saunders, Philippa T. K. [4 ]
Hay, David C. [1 ]
机构
[1] Univ Edinburgh, Inst Regenerat & Repair, Ctr Regenerat Med, Edinburgh BioQuarter, Edinburgh EH16 4UU, Scotland
[2] Univ Glasgow, Sch Biodivers, One Hlth, Vet Med, Glasgow G61 1QH, Scotland
[3] Univ Glasgow, Wellcome Ctr Integrat Parasitol, Glasgow G12 9TA, Scotland
[4] Univ Edinburgh, Inst Regenerat & Repair, Ctr Inflammat Res, Edinburgh BioQuarter, Edinburgh EH16 4UU, Scotland
基金
英国惠康基金; 英国医学研究理事会; 英国科研创新办公室;
关键词
liver; NAFLD; sex hormones; estrogen; testosterone; HRT; immune response; in vitro models; human PSCs; tissue engineering; ESTROGEN-RECEPTORS ALPHA; HEPATIC PROGENITOR CELLS; FATTY LIVER; INSULIN-RESISTANCE; ANDROGEN RECEPTOR; KUPFFER CELLS; BINDING GLOBULIN; DEPENDENT REGULATION; REPLACEMENT THERAPY; GLUCOSE-HOMEOSTASIS;
D O I
10.3390/cells12121604
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The liver performs a multitude of bodily functions, whilst retaining the ability to regenerate damaged tissue. In this review, we discuss sex steroid biology, regulation of mammalian liver physiology and the development of new model systems to improve our understanding of liver biology in health and disease. A major risk factor for the development of liver disease is hepatic fibrosis. Key drivers of this process are metabolic dysfunction and pathologic activation of the immune system. Although non-alcoholic fatty liver disease (NAFLD) is largely regarded as benign, it does progress to non-alcoholic steatohepatitis in a subset of patients, increasing their risk of developing cirrhosis and hepatocellular carcinoma. NAFLD susceptibility varies across the population, with obesity and insulin resistance playing a strong role in the disease development. Additionally, sex and age have been identified as important risk factors. In addition to the regulation of liver biochemistry, sex hormones also regulate the immune system, with sexual dimorphism described for both innate and adaptive immune responses. Therefore, sex differences in liver metabolism, immunity and their interplay are important factors to consider when designing, studying and developing therapeutic strategies to treat human liver disease. The purpose of this review is to provide the reader with a general overview of sex steroid biology and their regulation of mammalian liver physiology.
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页数:26
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共 202 条
  • [131] Developmental Phenotype of a Membrane Only Estrogen Receptor α(MOER) Mouse
    Pedram, Ali
    Razandi, Mahnaz
    Kim, Jin K.
    O'Mahony, Fiona
    Lee, Eva Y. H. P.
    Luderer, Ulrike
    Levin, Ellis R.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (06) : 3488 - 3495
  • [132] Liver fibrosis and repair: immune regulation of wound healing in a solid organ
    Pellicoro, Antonella
    Ramachandran, Prakash
    Iredale, John P.
    Fallowfield, Jonathan A.
    [J]. NATURE REVIEWS IMMUNOLOGY, 2014, 14 (03) : 181 - 194
  • [133] Does insulin resistance, visceral adiposity, or a sex hormone alteration underlie the metabolic syndrome? Studies in women
    Phillips, Gerald B.
    Jing, Tianyi
    Heymsfield, Steven B.
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 2008, 57 (06): : 838 - 844
  • [134] Sex steroids and sex hormone-binding globulin in postmenopausal women with nonalcoholic fatty liver disease
    Polyzos, Stergios A.
    Kountouras, Jannis
    Tsatsoulis, Agathocles
    Zafeiriadou, Efthimia
    Katsiki, Evangelia
    Patsiaoura, Kalliopi
    Zavos, Christos
    Anastasiadou, Vasiliki V.
    Slavakis, Aristidis
    [J]. HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM, 2013, 12 (03): : 405 - 416
  • [135] Purnell JQ., 2000, Endotext
  • [136] Sex Hormone-Binding Globulin (SHBG) as an Early Biomarker and Therapeutic Target in Polycystic Ovary Syndrome
    Qu, Xianqin
    Donnelly, Richard
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (21) : 1 - 17
  • [137] Liver fibrosis: a bidirectional model of fibrogenesis and resolution
    Ramachandran, P.
    Iredale, J. P.
    [J]. QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2012, 105 (09) : 813 - 817
  • [138] In vitro models for non-alcoholic fatty liver disease: Emerging platforms and their applications
    Ramos, Maria Jimenez
    Bandiera, Lucia
    Menolascina, Filippo
    Fallowfield, Jonathan Andrew
    [J]. ISCIENCE, 2022, 25 (01)
  • [139] 3D human liver tissue from pluripotent stem cells displays stable phenotype in vitro and supports compromised liver function in vivo
    Rashidi, Hassan
    Nguyet-Thin Luu
    Alwahsh, Salamah M.
    Ginai, Maaria
    Alhaque, Sharmin
    Dong, Hua
    Tomaz, Rute A.
    Vernay, Bertrand
    Vigneswara, Vasanthy
    Hallett, John M.
    Chandrashekran, Anil
    Dhawan, Anil
    Vallier, Ludovic
    Bradley, Mark
    Callanan, Anthony
    Forbes, Stuart J.
    Newsome, Philip N.
    Hay, David C.
    [J]. ARCHIVES OF TOXICOLOGY, 2018, 92 (10) : 3117 - 3129
  • [140] Progression from Nonalcoholic Fatty Liver to Nonalcoholic Steatohepatitis Is Marked by a Higher Frequency of Th17 Cells in the Liver and an Increased Th17/Resting Regulatory T Cell Ratio in Peripheral Blood and in the Liver
    Rau, Monika
    Schilling, Anne-Kristin
    Meertens, Jan
    Hering, Ilona
    Weiss, Johannes
    Jurowich, Christian
    Kudlich, Theodor
    Hermanns, Heike M.
    Bantel, Heike
    Beyersdorf, Niklas
    Geier, Andreas
    [J]. JOURNAL OF IMMUNOLOGY, 2016, 196 (01) : 97 - 105