Human Body Composition and Immunity: Visceral Adipose Tissue Produces IL-15 and Muscle Strength Inversely Correlates with NK Cell Function in Elderly Humans

被引:20
作者
Al-Attar, Ahmad [1 ]
Presnell, Steven R. [1 ]
Clasey, Jody L. [2 ]
Long, Douglas E. [3 ]
Walton, R. Grace [3 ]
Sexton, Morgan [1 ]
Starr, Marlene E. [4 ]
Kern, Philip A. [5 ]
Peterson, Charlotte A. [3 ]
Lutz, Charles T. [1 ,6 ]
机构
[1] Univ Kentucky, Coll Med, Dept Pathol & Lab Med, Lexington, KY 40506 USA
[2] Univ Kentucky, Coll Med, Dept Kinesiol & Hlth Promot, Lexington, KY USA
[3] Univ Kentucky, Coll Hlth Sci, Dept Rehabil Sci, Lexington, KY USA
[4] Univ Kentucky, Coll Med, Dept Surg, Lexington, KY USA
[5] Univ Kentucky, Coll Med, Dept Med, Div Endocrinol, Lexington, KY USA
[6] Univ Kentucky, Coll Med, Dept Microbiol Immunol & Mol Genet, Lexington, KY 40506 USA
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
关键词
natural killer cell; adipose tissue; IL-15; skeletal muscle strength; aging; INNATE LYMPHOID-CELLS; NATURAL-KILLER; INSULIN-RESISTANCE; SKELETAL-MUSCLE; POTENTIAL ROLE; OBESITY; INTERLEUKIN-15; ASSOCIATION; SARCOPENIA; MICE;
D O I
10.3389/fimmu.2018.00440
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural killer (NK) lymphocyte-mediated cytotoxicity and cytokine secretion control infections and cancers, but these crucial activities decline with age. NK cell development, homeostasis, and function require IL-15 and its chaperone, IL-15 receptor alpha (IL-15R alpha). Macrophages and dendritic cells (DC) are major sources of these proteins. We had previously postulated that additional IL-15 and IL-15R alpha is made by skeletal muscle and adipose tissue. These sources may be important in aging, when IL-15-producing immune cells decline. NK cells circulate through adipose tissue, where they may be exposed to local IL-15. The objectives of this work were to determine (1) if human muscle, subcutaneous adipose tissue (SAT), and visceral adipose tissue (VAT) are sources of IL-15 and IL-15 R alpha, and (2) whether any of these tissues correlate with NK cell activity in elderly humans. We first investigated IL-15 and IL-15R alpha RNA expression in paired muscle and SAT biopsies from healthy human subjects. Both tissues expressed these transcripts, but IL-15R alpha RNA levels were higher in SAT than in skeletal muscle. We also investigated tissue obtained from surgeries and found that SAT and VAT expressed equivalent amounts of IL-15 and IL-15R alpha RNA, respectively. Furthermore, stromal vascular fraction cells expressed more IL-15 RNA than did adipocytes. To test if these findings related to circulating IL-15 protein and NK cell function, we tested 50 healthy adults aged >70 years old. Plasma IL-15 levels significantly correlated with abdominal VAT mass in the entire cohort and in non-obese subjects. However, plasma IL-15 levels did not correlate with skeletal muscle cross-sectional area and correlated inversely with muscle strength. Plasma IL-15 did correlate with NK cell cytotoxic granule exocytosis and with CCL4 (MIP-1 beta) production in response to NKp46-crosslinking. Additionally, NK cell responses to K562 leukemia cells correlated inversely with muscle strength. With aging, immune function declines while infections, cancers, and deaths increase. We propose that VAT-derived IL-15 and IL-15R alpha is a compensatory NK cell support mechanism in elderly humans.
引用
收藏
页数:11
相关论文
共 48 条
[1]   The effect of sex on immune cells in healthy aging: Elderly women have more robust natural killer lymphocytes than do elderly men [J].
Al-Attar, Ahmad ;
Presnell, Steven R. ;
Peterson, Charlotte A. ;
Thomas, D. Travis ;
Lutz, Charles T. .
MECHANISMS OF AGEING AND DEVELOPMENT, 2016, 156 :25-33
[2]   Effects of IL-15 on rat brown adipose tissue:: Uncoupling proteins and PPARs [J].
Almendro, Vanessa ;
Fuster, Gemma ;
Busquets, Silvia ;
Ametller, Elisabet ;
Figueras, Maite ;
Argiles, Josep M. ;
Lopez-Soriano, Francisco J. .
OBESITY, 2008, 16 (02) :285-289
[3]   Effects of interleukin-15 (IL-15) on adipose tissue mass in rodent obesity models:: evidence for direct IL-15 action on adipose tissue [J].
Alvarez, B ;
Carbó, N ;
López-Soriano, J ;
Drivdahl, RH ;
Busquets, S ;
López-Soriano, FJ ;
Argilés, JM ;
Quinn, LS .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2002, 1570 (01) :33-37
[4]   Interleukin-15 Treatment Induces Weight Loss Independent of Lymphocytes [J].
Barra, Nicole G. ;
Chew, Marianne V. ;
Reid, Sarah ;
Ashkar, Ali A. .
PLOS ONE, 2012, 7 (06)
[5]   Interleukin-15 Contributes to the Regulation of Murine Adipose Tissue and Human Adipocytes [J].
Barra, Nicole G. ;
Reid, Sarah ;
MacKenzie, Randy ;
Werstuck, Geoff ;
Trigatti, Bernardo L. ;
Richards, Carl ;
Holloway, Alison C. ;
Ashkar, Ali A. .
OBESITY, 2010, 18 (08) :1601-1607
[6]   Circulating IL-15 exists as heterodimeric complex with soluble IL-15Rα in human and mouse serum [J].
Bergamaschi, Cristina ;
Bear, Jenifer ;
Rosati, Margherita ;
Beach, Rachel Kelly ;
Alicea, Candido ;
Sowder, Raymond ;
Chertova, Elena ;
Rosenberg, Steven A. ;
Felber, Barbara K. ;
Pavlakis, George N. .
BLOOD, 2012, 120 (01) :E1-E8
[7]   Adipose Type One Innate Lymphoid Cells Regulate Macrophage Homeostasis through Targeted Cytotoxicity [J].
Boulenouar, Selma ;
Michelet, Xavier ;
Duquette, Danielle ;
Alvarez, David ;
Hogan, Andrew E. ;
Dold, Christina ;
O'Connor, Donal ;
Stutte, Suzanne ;
Tavakkoli, Ali ;
Winters, Desmond ;
Exley, Mark A. ;
O'Shea, Donal ;
Brenner, Michael B. ;
von Andrian, Ulrich ;
Lynch, Lydia .
IMMUNITY, 2017, 46 (02) :273-286
[8]   Interleukin-15 mediates reciprocal regulation of adipose and muscle mass:: A potential role in body weight control [J].
Carbó, N ;
López-Soriano, J ;
Costelli, P ;
Alvarez, B ;
Busquets, S ;
Baccino, FM ;
Quinn, LS ;
López-Soriano, FJ ;
Argilés, JM .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2001, 1526 (01) :17-24
[9]  
Cawthon PM, 2013, GERONTOLOGIST, V53, P594, DOI 10.1093/gerona/glu023
[10]   The Host Environment Is Responsible for Aging-Related Functional NK Cell Deficiency [J].
Chiu, Bo-Chin ;
Martin, Brian E. ;
Stolberg, Valerie R. ;
Chensue, Stephen W. .
JOURNAL OF IMMUNOLOGY, 2013, 191 (09) :4688-4698