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Size matters: the biochemical logic of ligand type in endocrine crosstalk.
Lone, Jameel Barkat; Long, Jonathan Z; Svensson, Katrin J.
Afiliação
  • Lone JB; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Long JZ; Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Svensson KJ; Department of Chemistry, Stanford University, Stanford, CA 94305, USA.
Life Metab ; 3(1)2024 Feb.
Article em En | MEDLINE | ID: mdl-38425548
ABSTRACT
The endocrine system is a fundamental type of long-range cell-cell communication that is important for maintaining metabolism, physiology, and other aspects of organismal homeostasis. Endocrine signaling is mediated by diverse blood-borne ligands, also called hormones, including metabolites, lipids, steroids, peptides, and proteins. The size and structure of these hormones are fine-tuned to make them bioactive, responsive, and adaptable to meet the demands of changing environments. Why has nature selected such diverse ligand types to mediate communication in the endocrine system? What is the chemical, signaling, or physiologic logic of these ligands? What fundamental principles from our knowledge of endocrine communication can be applied as we continue as a field to uncover additional new circulating molecules that are claimed to mediate long-range cell and tissue crosstalk? This review provides a framework based on the biochemical logic behind this crosstalk with respect to their chemistry, temporal regulation in physiology, specificity, signaling actions, and evolutionary development.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article