The effect of bradykinin on the pro-inflammatory response of human adipocytes.


Journal

Acta biochimica Polonica
ISSN: 1734-154X
Titre abrégé: Acta Biochim Pol
Pays: Poland
ID NLM: 14520300R

Informations de publication

Date de publication:
10 Jul 2022
Historique:
received: 07 06 2022
accepted: 08 06 2022
pubmed: 11 7 2022
medline: 21 9 2022
entrez: 10 7 2022
Statut: ppublish

Résumé

The proper functioning of adipose tissue is one of the factors in maintaining energy homeostasis. Adipocytes not only store lipids but also produce active molecules such as adipokines and adipocytokines, which are involved in many functions of adipose tissue, including the secretion of hormones that regulate energy and lipid metabolism. Inflammation has been shown to underlie the deregulation of adipose tissue function. Bradykinin belongs to a family of pro-inflammatory kinin peptides that are abundant in most tissues and biological fluids. This study aimed to determine the ability to produce kinin peptides and characterize the effect of bradykinin on pro-inflammatory responses in adipocytes. The Chub-S7 human preadipocyte line was differentiated to show specific properties for adipose tissue cells. The differentiated cells expressed genes that encode proteins such as kininogen, kallikrein, and prolylcarboxypeptidase that are involved in the production of kinins and also showed the expression of kinin receptors. The response of adipocytes to bradykinin was examined in relation to kinin concentration and the presence of kininase inhibitors. The high concentration of bradykinin induced a moderate increase in lipid accumulation, increased release of pro-inflammatory cytokines, and altered gene expression of molecules involved in adipocyte function, such as adiponectin, lipoprotein lipase, and other transcription factors. This study suggests an important role for kinin peptides in inducing inflammatory responses in adipocytes, which can modify the function of adipose tissue and ultimately lead to diseases related to disturbance of energy homeostasis. The results obtained may enrich our understanding of the mechanisms underlying obesity-related disorders.

Identifiants

pubmed: 35810482
pii: 6389
doi: 10.18388/abp.2020_6389
doi:

Substances chimiques

Adipokines 0
Adiponectin 0
Cytokines 0
Kininogens 0
Lipids 0
Transcription Factors 0
Lipoprotein Lipase EC 3.1.1.34
Kallikreins EC 3.4.21.-
Bradykinin S8TIM42R2W

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

495-505

Auteurs

Ibeth Guevara-Lora (I)

Department of Analytical Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University in Krakow, Kraków, Poland.

Maria Sordyl (M)

Chair of Clinical Biochemistry, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.

Anna Niewiarowska-Sendo (A)

Department of Analytical Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University in Krakow, Kraków, Poland.

Grazyna Bras (G)

Department of Comparative Biochemistry and Bioanalytics, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University in Krakow, Kraków, Poland.

Edyta Korbut (E)

Department of Analytical Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University in Krakow, Kraków, Poland.

Joanna Goralska (J)

Chair of Clinical Biochemistry, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.

Malgorzata Malczewska-Malec (M)

Chair of Clinical Biochemistry, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.

Bogdan Solnica (B)

Chair of Clinical Biochemistry, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.

Andrzej Kozik (A)

Department of Analytical Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University in Krakow, Kraków, Poland.

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Classifications MeSH