دورية أكاديمية

Stage-dependent cardiac regeneration in Xenopus is regulated by thyroid hormone availability.

التفاصيل البيبلوغرافية
العنوان: Stage-dependent cardiac regeneration in Xenopus is regulated by thyroid hormone availability.
المؤلفون: Marshall LN; Evolution des Régulations Endocriniennes, Département Adaptation du vivant, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Sorbonne Université, 75231 Paris, France., Vivien CJ; Evolution des Régulations Endocriniennes, Département Adaptation du vivant, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Sorbonne Université, 75231 Paris, France.; Murdoch Children's Research Institute, The Royal Children's Hospital, Melbourne, VIC 3052, Australia., Girardot F; Evolution des Régulations Endocriniennes, Département Adaptation du vivant, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Sorbonne Université, 75231 Paris, France., Péricard L; Evolution des Régulations Endocriniennes, Département Adaptation du vivant, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Sorbonne Université, 75231 Paris, France., Scerbo P; Evolution des Régulations Endocriniennes, Département Adaptation du vivant, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Sorbonne Université, 75231 Paris, France.; Institut Curie, CNRS UMR 3347, INSERM U1021, Centre Universitaire, F-91405 Orsay, France., Palmier K; Evolution des Régulations Endocriniennes, Département Adaptation du vivant, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Sorbonne Université, 75231 Paris, France.; Institute for Integrative Biology of the Cell, Commissariat à l'Energie Atomique, CNRS UMR 9198, Université Paris Sud, Saclay, 91198 Gif-sur-Yvette, France., Demeneix BA; Evolution des Régulations Endocriniennes, Département Adaptation du vivant, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Sorbonne Université, 75231 Paris, France., Coen L; Evolution des Régulations Endocriniennes, Département Adaptation du vivant, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Sorbonne Université, 75231 Paris, France; coen@mnhn.fr.
المصدر: Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2019 Feb 26; Vol. 116 (9), pp. 3614-3623. Date of Electronic Publication: 2019 Feb 12.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1091-6490 (Electronic) Linking ISSN: 00278424 NLM ISO Abbreviation: Proc Natl Acad Sci U S A Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Washington, DC : National Academy of Sciences
مواضيع طبية MeSH: Heart Failure/*prevention & control , Regeneration/*genetics , Thyroid Hormones/*metabolism , Xenopus laevis/*genetics, Animals ; Gene Expression Regulation, Developmental/drug effects ; Heart Failure/physiopathology ; Humans ; Larva/genetics ; Larva/growth & development ; Metamorphosis, Biological/genetics ; Mice ; Salamandridae/genetics ; Salamandridae/growth & development ; Thyroid Hormones/administration & dosage ; Thyroid Hormones/genetics ; Xenopus laevis/growth & development ; Zebrafish/genetics ; Zebrafish/growth & development
مستخلص: Despite therapeutic advances, heart failure is the major cause of morbidity and mortality worldwide, but why cardiac regenerative capacity is lost in adult humans remains an enigma. Cardiac regenerative capacity widely varies across vertebrates. Zebrafish and newt hearts regenerate throughout life. In mice, this ability is lost in the first postnatal week, a period physiologically similar to thyroid hormone (TH)-regulated metamorphosis in anuran amphibians. We thus assessed heart regeneration in Xenopus laevis before, during, and after TH-dependent metamorphosis. We found that tadpoles display efficient cardiac regeneration, but this capacity is abrogated during the metamorphic larval-to-adult switch. Therefore, we examined the consequence of TH excess and deprivation on the efficiently regenerating tadpole heart. We found that either acute TH treatment or blocking TH production before resection significantly but differentially altered gene expression and kinetics of extracellular matrix components deposition, and negatively impacted myocardial wall closure, both resulting in an impeded regenerative process. However, neither treatment significantly influenced DNA synthesis or mitosis in cardiac tissue after amputation. Overall, our data highlight an unexplored role of TH availability in modulating the cardiac regenerative outcome, and present X. laevis as an alternative model to decipher the developmental switches underlying stage-dependent constraint on cardiac regeneration.
Competing Interests: The authors declare no conflict of interest.
References: Mol Carcinog. 1999 Feb;24(2):99-107. (PMID: 10078937)
Mol Endocrinol. 1999 Dec;13(12):2076-89. (PMID: 10598583)
Neurosci Lett. 2000 Feb 18;280(2):79-82. (PMID: 10686382)
Methods. 2001 Dec;25(4):402-8. (PMID: 11846609)
Biull Eksp Biol Med. 1975 Nov;80(11):111-3. (PMID: 1240779)
Science. 2002 Dec 13;298(5601):2188-90. (PMID: 12481136)
Circ Res. 1992 Oct;71(4):831-9. (PMID: 1381294)
Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3474-9. (PMID: 14993610)
Environ Toxicol Chem. 2005 Apr;24(4):926-33. (PMID: 15839568)
J Clin Invest. 2006 Oct;116(10):2571-9. (PMID: 17016550)
Dev Growth Differ. 2007 Feb;49(2):131-43. (PMID: 17335434)
Dev Biol. 2007 Jun 1;306(1):20-33. (PMID: 17449026)
Pharmacol Ther. 2007 Dec;116(3):391-400. (PMID: 17919732)
Genesis. 2008 Nov;46(11):657-72. (PMID: 18932261)
Heart Fail Rev. 2010 Mar;15(2):133-42. (PMID: 19107595)
Dev Dyn. 2009 Jun;238(6):1249-70. (PMID: 19253402)
Dev Dyn. 2009 Jun;238(6):1226-48. (PMID: 19280606)
Aquat Toxicol. 2010 Jun 1;98(1):44-50. (PMID: 20153061)
Best Pract Res Clin Endocrinol Metab. 2010 Feb;24(1):133-41. (PMID: 20172477)
J Mol Histol. 2010 Feb;41(1):39-50. (PMID: 20232238)
Eur J Cardiothorac Surg. 2010 Dec;38(6):691-8. (PMID: 20452780)
Toxicol Sci. 2010 Nov;118(1):42-51. (PMID: 20530234)
Circulation. 2010 Jul 27;122(4):385-93. (PMID: 20660814)
JAMA. 2011 Jan 5;305(1):87-8. (PMID: 21177496)
Science. 2011 Feb 25;331(6020):1078-80. (PMID: 21350179)
Nature. 2011 May 19;473(7347):326-35. (PMID: 21593865)
Thyroid. 2011 Aug;21(8):879-90. (PMID: 21745103)
FASEB J. 2012 Jan;26(1):397-408. (PMID: 21974928)
Development. 2012 Jun;139(11):1921-30. (PMID: 22513374)
Biochim Biophys Acta. 2013 Jul;1830(7):3937-45. (PMID: 22634734)
Nat Rev Mol Cell Biol. 2013 Aug;14(8):529-41. (PMID: 23839576)
Dev Biol. 2013 Oct 15;382(2):457-69. (PMID: 23939298)
Dev Biol. 2013 Oct 15;382(2):427-35. (PMID: 23988577)
Nat Rev Endocrinol. 2014 Apr;10(4):206-14. (PMID: 24322650)
Curr Treat Options Cardiovasc Med. 2014 Mar;16(3):288. (PMID: 24496965)
Dev Dyn. 2014 Sep;243(9):1106-15. (PMID: 24947076)
Physiol Rep. 2014 Aug 28;2(8):null. (PMID: 25168870)
Nat Rev Mol Cell Biol. 2014 Dec;15(12):786-801. (PMID: 25415508)
J Endocrinol. 2015 Jun;225(3):R67-81. (PMID: 25972358)
Hypertension. 2015 Oct;66(4):757-66. (PMID: 26238448)
Circ Res. 2016 Jan 22;118(2):216-21. (PMID: 26659640)
Eur J Heart Fail. 2016 Apr;18(4):375-85. (PMID: 26763891)
Heart Fail Rev. 2016 Jul;21(4):391-9. (PMID: 27011011)
Open Biol. 2016 Mar;6(3):null. (PMID: 27030176)
Nat Rev Cardiol. 2017 Jan;14(1):39-55. (PMID: 27811932)
J Neuromuscul Dis. 2016 Nov 29;3(4):455-473. (PMID: 27911334)
Sci Adv. 2016 Nov 18;2(11):e1600844. (PMID: 28138518)
Immunol Lett. 2017 Apr;184:76-83. (PMID: 28216261)
PLoS One. 2017 Mar 9;12(3):e0173418. (PMID: 28278282)
Cell Biosci. 2017 Mar 21;7:14. (PMID: 28331574)
Dev Neurobiol. 2017 Sep;77(9):1086-1100. (PMID: 28371543)
J Clin Invest. 2017 May 1;127(5):1600-1612. (PMID: 28459429)
Nature. 2017 Jul 13;547(7662):179-184. (PMID: 28581497)
Science. 2017 Jun 9;356(6342):1035-1039. (PMID: 28596337)
Mol Cell Endocrinol. 2017 Dec 25;459:79-83. (PMID: 28630021)
Elife. 2017 Jun 20;6:. (PMID: 28632131)
Eur Thyroid J. 2017 Jul;6(3):130-137. (PMID: 28785539)
NPJ Regen Med. 2017;2:null. (PMID: 29201433)
Cell Biosci. 2017 Dec 13;7:70. (PMID: 29255592)
NPJ Regen Med. 2016 Jul 28;1:16012. (PMID: 29302337)
Cell Biosci. 2018 Apr 19;8:31. (PMID: 29713454)
Circulation. 2018 Dec 11;138(24):2798-2808. (PMID: 30030417)
Arkh Patol. 1977 Jan;39(1):53-8. (PMID: 843235)
J Immunol. 1996 Jan 1;156(1):1-4. (PMID: 8598448)
Neuroscience. 1998 May;84(1):309-22. (PMID: 9580330)
فهرسة مساهمة: Keywords: Xenopus; cardiac regeneration; extracellular matrix; metamorphosis; thyroid hormone
المشرفين على المادة: 0 (Thyroid Hormones)
تواريخ الأحداث: Date Created: 20190214 Date Completed: 20190502 Latest Revision: 20200225
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC6397552
DOI: 10.1073/pnas.1803794116
PMID: 30755533
قاعدة البيانات: MEDLINE
الوصف
تدمد:1091-6490
DOI:10.1073/pnas.1803794116