» Articles » PMID: 11607571

Whole-body Protochordate Regeneration from Totipotent Blood Cells

Overview
Specialty Science
Date 1995 Aug 15
PMID 11607571
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Cell differentiation, tissue formation, and organogenesis are fundamental patterns during the development of multicellular animals from the dividing cells of fertilized eggs. Hence, the complete morphogenesis of any developing organism of the animal kingdom is based on a complex series of interactions that is always associated with the development of a blastula, a one-layered hollow sphere. Here we document an alternative pathway of differentiation, organogenesis, and morphogenesis occurring in an adult protochordate colonial organism. In this system, any minute fragment of peripheral blood vessel containing a limited number of blood cells isolated from Botrylloides, a colonial sea squirt, has the potential to give rise to a fully functional organism possessing all three embryonic layers. Regeneration probably results from a small number of totipotent stem cells circulating in the blood system. The developmental process starts from disorganized, chaotic masses of blood cells. At first an opaque cell mass is formed. Through intensive cell divisions, a hollow, blastula-like structure results, which may produce a whole organism within a short period of a week. This regenerative power of the protochordates may be compared with some of the characteristics associated with the formation of mammalian embryonal carcinomous bodies. It may also serve as an in vivo model system for studying morphogenesis and differentiation by shedding more light on the controversy of the "stem cell" vs. the "dedifferentiation" theories of regeneration and pattern formation.

Citing Articles

The salamander blastema within the broader context of metazoan regeneration.

Tajer B, Savage A, Whited J Front Cell Dev Biol. 2023; 11:1206157.

PMID: 37635872 PMC: 10450636. DOI: 10.3389/fcell.2023.1206157.


De novo genome assembly and comparative genomics for the colonial ascidian Botrylloides violaceus.

Sumner J, Andrasz C, Johnson C, Wax S, Anderson P, Keeling E G3 (Bethesda). 2023; 13(10).

PMID: 37555394 PMC: 10542563. DOI: 10.1093/g3journal/jkad181.


Differentially expressed chaperone genes reveal a stress response required for unidirectional regeneration in the basal chordate Ciona.

Jeffery W, Li B, Ng M, Li L, Goricki S, Ma L BMC Biol. 2023; 21(1):148.

PMID: 37365564 PMC: 10294541. DOI: 10.1186/s12915-023-01633-y.


Noninvasive Intravascular Microtransfusion in Colonial Tunicates.

Serrato L, Bilella A, Blanchoud S Methods Mol Biol. 2022; 2450:399-415.

PMID: 35359320 PMC: 9761924. DOI: 10.1007/978-1-0716-2172-1_21.


Studying Tunicata WBR Using Botrylloides anceps.

Karahan A, Ozturk E, Temiz B, Blanchoud S Methods Mol Biol. 2022; 2450:311-332.

PMID: 35359315 PMC: 9761534. DOI: 10.1007/978-1-0716-2172-1_16.


References
1.
Martin G . Teratocarcinomas as a model system for the study of embryogenesis and neoplasia. Cell. 1975; 5(3):229-43. DOI: 10.1016/0092-8674(75)90098-7. View

2.
Pierce G, DIXON Jr F . Testicular teratomas. I. Demonstration of teratogenesis by metamorphosis of multipotential cells. Cancer. 1959; 12(3):573-83. DOI: 10.1002/1097-0142(195905/06)12:3<573::aid-cncr2820120316>3.0.co;2-m. View

3.
Sleigh M . Differentiation and proliferation in mouse embryonal carcinoma cells. Bioessays. 1992; 14(11):769-75. DOI: 10.1002/bies.950141109. View

4.
De Loof A . All animals develop from a blastula: consequences of an undervalued definition for thinking on development. Bioessays. 1992; 14(8):573-5. DOI: 10.1002/bies.950140815. View

5.
Freeman G . THE ROLE OF BLOOD CELLS IN THE PROCESS OF ASEXUAL REPORODUCTION IN THE TUNICATE PEROPHORA VIRIDIS. J Exp Zool. 1964; 156:157-83. DOI: 10.1002/jez.1401560204. View