Regeneration of the flatworm Prosthiostomum siphunculus (Polycladida, Platyhelminthes).
Blastema
Flatworm
Polyclad
Proliferation
Regeneration
Journal
Cell and tissue research
ISSN: 1432-0878
Titre abrégé: Cell Tissue Res
Pays: Germany
ID NLM: 0417625
Informations de publication
Date de publication:
Mar 2021
Mar 2021
Historique:
received:
05
05
2020
accepted:
14
09
2020
pubmed:
8
11
2020
medline:
2
10
2021
entrez:
7
11
2020
Statut:
ppublish
Résumé
Fueled by the discovery of head regeneration in triclads (planarians) two and a half centuries ago, flatworms have been the focus of regeneration research. But not all flatworms can regenerate equally well and to obtain a better picture of the characteristics and evolution of regeneration in flatworms other than planarians, the regeneration capacity and stem cell dynamics during regeneration in the flatworm order Polycladida are studied. Here, we show that as long as the brain remained at least partially intact, the polyclad Prosthiostomum siphunculus was able to regenerate submarginal eyes, cerebral eyes, pharynx, intestine and sucker. In the complete absence of the brain only wound closure was observed but no regeneration of missing organs. Amputated parts of the brain could not be regenerated. The overall regeneration capacity of P. siphunculus is a good fit for category III after a recently established system, in which most polyclads are currently classified. Intact animals showed proliferating cells in front of the brain which is an exception compared with most of the other free-living flatworms that have been observed so far. Proliferating cells could be found within the regeneration blastema, similar to all other flatworm taxa except triclads. No proliferation was observed in epidermis and pharynx. In pulse-chase experiments, the chased cells were found in all regenerated tissues and thereby shown to differentiate and migrate to replace the structures lost upon amputation.
Identifiants
pubmed: 33159580
doi: 10.1007/s00441-020-03302-w
pii: 10.1007/s00441-020-03302-w
pmc: PMC7960593
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1025-1041Références
Zoological Lett. 2019 Feb 12;5:7
pubmed: 30805201
BMC Dev Biol. 2009 Jul 15;9:41
pubmed: 19604404
Evodevo. 2013 Oct 09;4(1):29
pubmed: 24107307
Cell Tissue Res. 2007 Mar;327(3):637-46
pubmed: 17043794
J Embryol Exp Morphol. 1984 Oct;83:63-80
pubmed: 6502076
PLoS One. 2009;4(5):e5502
pubmed: 19430533
Nat Methods. 2012 Jun 28;9(7):676-82
pubmed: 22743772
Cell Tissue Res. 2015 Dec;362(3):529-40
pubmed: 26104134
Dev Biol. 2000 Apr 15;220(2):142-53
pubmed: 10753506
J Exp Zool. 1974 Mar;187(3):335-44
pubmed: 4820342
Biol Bull. 1976 Jun;150(3):411-25
pubmed: 953071
Science. 2011 May 13;332(6031):811-6
pubmed: 21566185
Cell Tissue Res. 2020 Feb;379(2):301-321
pubmed: 31511984
Trans Am Microsc Soc. 1974 Jul;93(3):386-91
pubmed: 4853459
Annu Rev Cell Dev Biol. 2004;20:725-57
pubmed: 15473858
J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2010 May;196(5):359-68
pubmed: 20339850
Evodevo. 2012 Mar 19;3:7
pubmed: 22429930
Cell Tissue Res. 2012 Aug;349(2):517-25
pubmed: 22729484
J Exp Zool. 1985 Aug;235(2):157-73
pubmed: 4056686
Dev Genes Evol. 1997 Nov;207(5):306-316
pubmed: 27747428
Wilhelm Roux Arch Entwickl Mech Org. 1939 Dec;139(4):780-818
pubmed: 28353994
Evodevo. 2014 Oct 23;5:37
pubmed: 25908954
Dev Genes Evol. 2006 Oct;216(10):565-77
pubmed: 16604349
J Neurobiol. 1980 Sep;11(5):483-96
pubmed: 7420083