Rabiller Lise, Labit Elodie, Guissard Christophe, Gilardi Silveric, Guiard Bruno P, Moulédous Lionel, Silva Marine, Mithieux Gilles, Pénicaud Luc, Lorsignol Anne, Casteilla Louis, Dromard Cécile
RESTORE, UMR INSERM 1301/CNRS 5070/Université Paul Sabatier/EFS/ENVT, Toulouse, France.
Department of Physiology and Cell Information Systems, McGill University, Montreal, QC, Canada.
NPJ Regen Med. 2021 Oct 14;6(1):63. doi: 10.1038/s41536-021-00175-7.
Tissue repair after injury in adult mammals, usually results in scarring and loss of function in contrast to lower vertebrates such as the newt and zebrafish that regenerate. Understanding the regulatory processes that guide the outcome of tissue repair is therefore a concerning challenge for regenerative medicine. In multiple regenerative animal species, the nerve dependence of regeneration is well established, but the nature of the innervation required for tissue regeneration remains largely undefined. Using our model of induced adipose tissue regeneration in adult mice, we demonstrate here that nociceptive nerves promote regeneration and their removal impairs tissue regeneration. We also show that blocking the receptor for the nociceptive neuropeptide calcitonin gene-related peptide (CGRP) inhibits regeneration, whereas CGRP administration induces regeneration. These findings reveal that peptidergic nociceptive neurons are required for adult mice tissue regeneration.
与蝾螈和斑马鱼等能够再生的低等脊椎动物不同,成年哺乳动物受伤后的组织修复通常会导致瘢痕形成和功能丧失。因此,了解指导组织修复结果的调控过程是再生医学面临的一个重要挑战。在多种具有再生能力的动物物种中,再生对神经的依赖性已得到充分证实,但组织再生所需的神经支配的本质仍很大程度上未明确。利用我们在成年小鼠中诱导脂肪组织再生的模型,我们在此证明伤害性神经促进再生,去除它们会损害组织再生。我们还表明,阻断伤害性神经肽降钙素基因相关肽(CGRP)的受体可抑制再生,而给予CGRP则可诱导再生。这些发现揭示了肽能伤害性神经元是成年小鼠组织再生所必需的。