Circulating Follistatin Is Liver-Derived and Regulated by the Glucagon-to-Insulin Ratio.

J Clin Endocrinol Metab

The Centre of Inflammation and Metabolism and the Centre for Physical Activity Research (J.S.H., B.K.P., P.P.), Rigshospitalet, University of Copenhagen, Denmark 2100; Department of Clinical Biochemistry (J.S.H., P.P.), Rigshospitalet, Copenhagen, Denmark 2100; Department of Genetic Medicine and Development (S.R., C.A., P.A.H., K.B.), University Medical Centre, University of Geneva, Geneva, Switzerland 1206; Department of Hepatology (J.O.C.), Rigshospitalet, Copenhagen, Denmark 2100; Department of Anaesthesiology (N.H.S.), The Copenhagen Muscle Research Centre, Rigshospitalet, Copenhagen, Denmark 2100; Division of Pathobiochemistry and Clinical Chemistry (A.D., C.W.), Department of Internal Medicine IV, University Tuebingen, Germany 72076; University Hospitals of Geneva (C.G.-G.), Surgical Research Unit, Geneva, Switzerland 1206; Institute for Diabetes Research and Metabolic Diseases of the Helmholtz Zentrum München (C.W.), University of Tuebingen, Tuebingen, Germany 72076; German Center for Diabetes Research (C.W.), München-Neuherberg, Germany 85764.

Published: February 2016

AI Article Synopsis

  • Follistatin, a plasma protein that increases during negative energy balance situations like exercise and fasting, is primarily secreted by the liver in humans, indicating its potential as an endocrine signal.
  • The secretion of follistatin is influenced by the glucagon-to-insulin ratio, with glucagon enhancing and insulin suppressing its release, which operates through the secondary messenger cAMP in liver cells.
  • Short-term exposure to follistatin decreases glucagon secretion from pancreatic islets, while long-term exposure protects and encourages the growth of rat insulin-producing cells.

Article Abstract

Context: Follistatin is a plasma protein recently reported to increase under conditions with negative energy balance, such as exercise and fasting in humans. Currently, the perception is that circulating follistatin is a result of para/autocrine actions from various tissues. The large and acute increase in circulating follistatin in response to exercise suggests that it may function as an endocrine signal.

Objective: We assessed origin and regulation of circulating follistatin in humans.

Design/interventions: First, we assessed arterial-to-venous difference of follistatin over the splanchnic bed at rest and during exercise in healthy humans. To evaluate the regulation of plasma follistatin we manipulated glucagon-to-insulin ratio in humans at rest as well as in cultured hepatocytes. Finally, the impact of follistatin on human islets of Langerhans was assessed.

Results: We demonstrate that in humans the liver is a major contributor to circulating follistatin both at rest and during exercise. Glucagon increases and insulin inhibits follistatin secretion both in vivo and in vitro, mediated via the secondary messenger cAMP in the hepatocyte. Short-term follistatin treatment reduced glucagon secretion from islets of Langerhans, whereas long-term follistatin treatment prevented apoptosis and induced proliferation of rat β cells.

Conclusions: In conclusion, in humans, the liver secretes follistatin at rest and during exercise, and the glucagon-to-insulin ratio is a key determinant of circulating follistatin levels. Circulating follistatin may be a marker of the glucagon-to-insulin tone on the liver.

Download full-text PDF

Source
http://dx.doi.org/10.1210/jc.2015-3668DOI Listing

Publication Analysis

Top Keywords

circulating follistatin
28
follistatin
14
glucagon-to-insulin ratio
12
rest exercise
12
islets langerhans
8
humans liver
8
follistatin rest
8
follistatin treatment
8
circulating
7
exercise
5

Similar Publications

Article Synopsis
  • * It used family-based statistical analysis methods to find that there is a significant genetic component influencing both LBP_DS and the measured body composition aspects and adipokines.
  • * The results suggest that different genetic factors impact LBP_DS, showing a complex relationship where adipokine variations and body composition measurements may independently affect back pain disability without overlapping genetic influences.
View Article and Find Full Text PDF

The Activin-A precursor dimer can be cleaved by furin, but how this proteolytic maturation is regulated in vivo and how it facilitates access to signaling receptors is unclear. Here, analysis in a syngeneic melanoma grafting model shows that without furin coexpression, Activin-A failed to accelerate tumor growth, correlating with failure of one or both subunits to undergo cleavage in signal-sending cells, even though compensatory processing by host cells nonetheless sustained elevated circulating Activin-A levels. In reporter assays, furin-independent cleavage of one subunit enabled juxtacrine Activin-A signaling, whereas completion of proteolytic maturation by coexpressed furin or by recipient cells stimulated contact-independent activity, crosstalk with BMP receptors, and signal inhibition by follistatin.

View Article and Find Full Text PDF

Background: Some experimental data suggest that myokines may play an important role in developing cancer-associated cachexia (CAC), but their relevance in humans remains poorly explored. In our study, we tested the hypothesis that circulating myokines are associated with the pathogenesis of CAC in a model population of gastric cancer.

Methods: A group of 171 treatment naïve patients with adenocarcinoma of the stomach were prospectively examined.

View Article and Find Full Text PDF

Plasma proteome and incident myocardial infarction: sex-specific differences.

Eur Heart J

November 2024

Unit of Medical Epidemiology, Department of Surgical Sciences, Uppsala University, Dag Hammarskjölds väg 14 B, 75185, Uppsala, Sweden.

Background And Aims: Few population-based cohort studies, including both men and women, have explored circulating proteins associated with incident myocardial infarction (MI). This study investigated the relationships between circulating cardiometabolic-related proteins and MI risk using cohort-based and Mendelian randomization (MR) analyses and explored potential sex-specific differences.

Methods: The discovery cohort included 11 751 Swedish adults (55-93 years).

View Article and Find Full Text PDF

Background: Testosterone (T) therapy increases lean mass and reduces total body and truncal fat mass in hypogonadal men. However, the underlying molecular mechanisms for the reciprocal changes in fat and lean mass in humans are not entirely clear.

Methods: Secondary analysis of specimens obtained from a single-arm, open-label clinical trial on pharmacogenetics of response to T therapy in men with late-onset hypogonadism, conducted between 2011 and 2016 involving 105 men (40-74 years old), who were given intramuscular T cypionate 200 mg every 2 weeks for 18 months.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!