Regeneration of the digestive system in the crinoid Himerometra robustipinna occurs by transdifferentiation of neurosecretory-like cells
- PMID: 28753616
- PMCID: PMC5533335
- DOI: 10.1371/journal.pone.0182001
Regeneration of the digestive system in the crinoid Himerometra robustipinna occurs by transdifferentiation of neurosecretory-like cells
Abstract
The structure and regeneration of the digestive system in the crinoid Himerometra robustipinna (Carpenter, 1881) were studied. The gut comprises a spiral tube forming radial lateral processes, which gives it a five-lobed shape. The digestive tube consists of three segments: esophagus, intestine, and rectum. The epithelia of these segments have different cell compositions. Regeneration of the gut after autotomy of the visceral mass progresses very rapidly. Within 6 h after autotomy, an aggregation consisting of amoebocytes, coelomic epithelial cells and juxtaligamental cells (neurosecretory neurons) forms on the inner surface of the skeletal calyx. At 12 h post-autotomy, transdifferentiation of the juxtaligamental cells starts. At 24 h post-autotomy these cells undergo a mesenchymal-epithelial-like transition, resulting in the formation of the luminal epithelium of the gut. Specialization of the intestinal epithelial cells begins on day 2 post-autotomy. At this stage animals acquire the mouth and anal opening. On day 4 post-autotomy the height of both the enterocytes and the visceral mass gradually increases. Proliferation does not play any noticeable role in gut regeneration. The immersion of animals in a 10-7 M solution of colchicine neither stopped formation of the lost structures nor caused accumulation of mitoses in tissues. Weakly EdU-labeled nuclei were observed in the gut only on day 2 post-autotomy and were not detected at later regeneration stages. Single mitotically dividing cells were recorded during the same period. It is concluded that juxtaligamental cells play a major role in gut regeneration in H. robustipinna. The main mechanisms of morphogenesis are cell migration and transdifferentiation.
Conflict of interest statement
Figures











Similar articles
-
Regeneration of the digestive system in the crinoid Lamprometra palmata (Mariametridae, Comatulida).Cell Tissue Res. 2023 Jan;391(1):87-109. doi: 10.1007/s00441-021-03526-4. Epub 2021 Oct 11. Cell Tissue Res. 2023. PMID: 34633568
-
Autotomy of the Visceral mass in the feather star Himerometra robustipinna (Crinoidea, Comatulida).Biol Bull. 2014 Apr;226(2):81-91. doi: 10.1086/BBLv226n2p81. Biol Bull. 2014. PMID: 24797090
-
Microscopic anatomy of the digestive system in normal and regenerating specimens of the brittlestar Amphipholis kochii.Biol Bull. 2010 Jun;218(3):303-16. doi: 10.1086/BBLv218n3p303. Biol Bull. 2010. PMID: 20570853
-
Morphological, Physiological and Mechanical Features of the Mutable Collagenous Tissues Associated with Autotomy and Evisceration in Dendrochirotid Holothuroids.Mar Drugs. 2023 Feb 21;21(3):134. doi: 10.3390/md21030134. Mar Drugs. 2023. PMID: 36976183 Free PMC article. Review.
-
Autotomy as a prelude to regeneration in echinoderms.Microsc Res Tech. 2001 Dec 15;55(6):369-96. doi: 10.1002/jemt.1185. Microsc Res Tech. 2001. PMID: 11782069 Review.
Cited by
-
Collective Locomotion of Human Cells, Wound Healing and Their Control by Extracts and Isolated Compounds from Marine Invertebrates.Molecules. 2020 May 26;25(11):2471. doi: 10.3390/molecules25112471. Molecules. 2020. PMID: 32466475 Free PMC article. Review.
-
A pan-metazoan concept for adult stem cells: the wobbling Penrose landscape.Biol Rev Camb Philos Soc. 2022 Feb;97(1):299-325. doi: 10.1111/brv.12801. Epub 2021 Oct 6. Biol Rev Camb Philos Soc. 2022. PMID: 34617397 Free PMC article.
-
Beyond Adult Stem Cells: Dedifferentiation as a Unifying Mechanism Underlying Regeneration in Invertebrate Deuterostomes.Front Cell Dev Biol. 2020 Oct 20;8:587320. doi: 10.3389/fcell.2020.587320. eCollection 2020. Front Cell Dev Biol. 2020. PMID: 33195242 Free PMC article. Review.
-
The Role of the Microbiota in Regeneration-Associated Processes.Front Cell Dev Biol. 2022 Jan 26;9:768783. doi: 10.3389/fcell.2021.768783. eCollection 2021. Front Cell Dev Biol. 2022. PMID: 35155442 Free PMC article. Review.
-
Molecular Aspects of Regeneration Mechanisms in Holothurians.Genes (Basel). 2021 Feb 10;12(2):250. doi: 10.3390/genes12020250. Genes (Basel). 2021. PMID: 33578707 Free PMC article. Review.
References
-
- Becker SF, Jarriault S (2016) Natural and induced direct reprogramming: mechanisms, concepts and general principles—from the worm to vertebrates. Current Opinion in Genetics & Development 40: 154–163. - PubMed
-
- Eguchi G, Kodama R (1993) Transdifferentiation. Current Opinion in Cell Biology 5: 1023–1028. - PubMed
-
- Eguizabal C, Montserrat N, Veiga A, Belmonte JCI (2013) Dedifferentiation, transdifferentiation, and reprogramming: future irections in regenerative medicine. Seminars in Reproductive Medicine 31: 082–094. - PubMed
-
- Fu L, Zhu X, Yi F, Liu G-H, Belmonte JCI (2014) Regenerative medicine: transdifferentiation in vivo. Cell Research 24: 141–142. doi: 10.1038/cr.2013.165 - DOI - PMC - PubMed
-
- Hu CP, Wu XR, Li QG, Sun ZW, Wang AP, Feng JT, et al. (2013) Proteomic analysis of NGF-induced transdifferentiation of adrenal medullary cells. International Journal of Molecular Medicine 32: 347–354. doi: 10.3892/ijmm.2013.1387 - DOI - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous