Abstract
Obesity is the commonest nutritional disorder of companion animals. In rodents and
humans, white adipose tissue is a major endocrine and secretory organ, releasing adipokines
linked to inflammation. In this study, we examined whether nerve growth factor (NGF),
a target-derived neurotrophin central to the development/maintenance of sympathetic
innervation and an inflammatory response protein, is synthesized and secreted by canine
adipocytes. NGF mRNA was detected in each of the major fat depots (the subcutaneous,
inguinal, gonadal, perirenal, and falciform ligaments) of dogs at similar levels.
Canine adipocytes, differentiated from preadipocytes (inguinal depot) in primary culture,
expressed the NGF gene and secreted NGF both pre- and post-differentiation. Treatment
of the differentiated adipocytes with LPS resulted in a dramatic increase in NGF mRNA
levels (20-fold at 24 h) and in NGF protein in the medium (60-fold at 24 h). The proinflammatory
cytokine TNFα also led to a substantial increase in NGF mRNA levels (11-fold) and
protein secretion (16-fold), while IL-6 had little effect. In contrast, dexamethasone
decreased both NGF mRNA levels (80%) and protein release (60%). The PPARγ agonist
rosiglitazone also reduced NGF secretion. These results demonstrate that canine white
adipocytes synthesize and secrete NGF, the powerful upregulation by LPS and TNFα indicating
that the neurotrophin is strongly linked to the inflammatory response in canine WAT.
Canine adipocytes appear highly sensitive to inflammatory stimuli.
Key words
adipokines - adipose tissue - inflammation - mRNA - neurotrophin - preadipocytes
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Correspondence
Prof. P. TrayhurnFRSE
Obesity Biology Research Unit
School of Clinical Sciences
University of Liverpool
Duncan Building
Liverpool L69 3GA
United Kingdom
Phone: +44/151/706 40 33
Fax: +44/151/706 58 02
Email: p.trayhurn@liverpool.ac.uk