涡虫肌肉系统再生研究进展
Research Progress in Nervous Regeneration of Planarians
DOI: 10.12677/BP.2021.113004, PDF,   
作者: 朱纯霄, 曹俊伟, 周欢敏, 张焱如, 刘春霞*:内蒙古农业大学生命科学学院,内蒙古 呼和浩特;内蒙古自治区生物制造重点实验室,内蒙古 呼和浩特;乌尼尔夫:内蒙古农业大学动物医学学院,内蒙古 呼和浩特
关键词: 肌肉极性Neoblast涡虫 Muscle Polarity Neoblast Planarian
摘要: 涡虫结构简单,具有极强的再生能力。再生,是指机体受损后,细胞、组织和器官的修复,并重建适当的组织极性、结构。在同一动物的不同组织中可以采用多种模式。当受到创伤后,涡虫的任意部位均可以再生出完整的个体。这种强大的再生能力是由neoblast介导的,neoblast是一种含有多能干细胞的增殖细胞群,具有异质性。涡虫具有明显的极性,受损后,严格按照前后轴、背腹轴、左右轴进行再生。涡虫有发达的体壁肌肉组织,在整个有机体内形成复杂的肌肉网络。涡虫的体壁肌肉细胞产生的位置信息基因(position control genes, PCGs),在再生过程中控制前后模式,对干细胞介导的组织替换和再生起着重要的指导作用。文章讨论了涡虫肌肉再生以及肌肉与极性基因之间的联系。
Abstract: The planarian has a simple structure and strong regeneration ability. Regeneration refers to the repair of cells, tissues and organs and the reconstruction of appropriate tissue polarity, structure, and form. Multiple models can be used in different tissues of the same animals. When traumatized, planarians can regenerate intact organisms. This powerful regeneration ability is mediated by neoblast, a kind of proliferation cell population containing pluripotent stem cells with heterogeneity. After being damaged, the planarian regenerates in strict accordance with the anteroposterior axis, dorsal ventral axis and left and right axis. Planarian has developed muscle tissue of body wall, forming complex muscle network in the whole organism. The signal molecules produced by the muscle cells in the body wall of planarians control the pre- and post-modes cells in the process of regeneration. Positional information genes (PCGs) mainly exist in muscle tissue and play an important role in guiding stem cell-mediated tissue replacement and regeneration. Muscle regeneration and the relationship between muscle and polar genes were discussed.
文章引用:朱纯霄, 乌尼尔夫, 曹俊伟, 周欢敏, 张焱如, 刘春霞. 涡虫肌肉系统再生研究进展[J]. 生物过程, 2021, 11(3): 30-37. https://doi.org/10.12677/BP.2021.113004

参考文献

[1] 陈广文, 吕九全, 马金友, 等. 我国的淡水涡虫[J]. 生物学通报, 2000(7): 15-17+52.
[2] Reddien, P.W. (2018) The Cellular and Molecular Basis for Planarian Regeneration. Cell, 175, 327-345. [Google Scholar] [CrossRef] [PubMed]
[3] Fincher, C.T., Wurtzel, O., Hoog, T.D., et al. (2018) Cell Type Transcriptome Atlas for the Planarian Schmidtea mediterranea. Science, 360, eaaq1736. [Google Scholar] [CrossRef] [PubMed]
[4] Raz, A.A., Wurtzel, O. and Reddien, P.W. (2021) Planarian Stem Cells Specify Fate Yet Retain Potency during the Cell Cycle. Cell Stem Cell, 28, 1307-1322.e5.
[5] Cutie, S., Hoang, A.T., Payumo, A.Y., et al. (2017) Unconventional Functions of Muscles in Planarian Regeneration. Developmental Cell, 43, 657-658. [Google Scholar] [CrossRef] [PubMed]
[6] Scimone, M.L., Cote, L.E. and Reddien, P.W. (2017) Orthogonal Muscle Fibres Have Different Instructive Roles in Planarian Regeneration. Nature, 551, 623-628. [Google Scholar] [CrossRef] [PubMed]
[7] Witchley, J., Mayer, M., Wagner, D., et al. (2013) Muscle Cells Provide Instructions for Planarian Regeneration. Cell Reports, 4, 633-641. [Google Scholar] [CrossRef] [PubMed]
[8] MacRae, E.K. (1963) Observation on the Fine Structure of Phar-yngeal Muscle in the Planarian Dugesia tigrina. Journal of Cell Biology, 18, 651-662. [Google Scholar] [CrossRef] [PubMed]
[9] Hanson, J. (1956) The Structure of the Smooth Muscle Fibres in the Body Wall of the Earthworm. The Journal of Biophysical and Biochemical Cytology, 3, 111-127. [Google Scholar] [CrossRef] [PubMed]
[10] Hori, I. (1983) Differentiation of Myoblasts in the Regeneationg Planarian Dugesia japonica. Cell Differentiation, 12, 155-163. [Google Scholar] [CrossRef
[11] Hartman, M. and Spudich, J.A. (2012) The Myosin Superfamily at a Glance. Journal of Cell Science, 125, 1627-1632. [Google Scholar] [CrossRef] [PubMed]
[12] Cebrià, F. (2000) Determination, Differentiation and Restitution of the Muscle Pattern during Regeneration and Cell Renewal in Freshwater Planarians. Ph.D. Thesis, University of Barcelona, Barcelona.
[13] Barany, M. (1967) ATPase Activity of Myosin Correlated with Speed of Muscle Shortening. The Journal of General Physiology, 50, 197-218. [Google Scholar] [CrossRef] [PubMed]
[14] Davis, R.L., Weintraub, H. and Lassar, A.B. (1988) Expression of a Single Transfected cDNA Converts Fibroblasts to Myoblasts. Cell, 51, 987-1000. [Google Scholar] [CrossRef
[15] Reddien, M. (2011) A Bmp/Admp Regulatory Circuit Controls Maintenance and Regeneration of Dorsal-Ventral Polarity in Planarians. Current Biology, 21, 294-299.
[16] Gurley, K.A., Rink, J.C. and Sanchez Alvarado, A. (2008) Beta-Catenin Defines Head versus Tail Iden-tity during Planarian Regeneration and Homeostasis. Science, 319, 323-327. [Google Scholar] [CrossRef] [PubMed]
[17] Iglesias, M., et al. (2008) Silencing of Smed-betacatenin1 Generates Radial-Like Hypercephalized Planarians. Development, 135, 1215-1221. [Google Scholar] [CrossRef] [PubMed]
[18] Petersen, C.P. and Reddien, P.W. (2008) Smed-betacatenin-1 Is Required for Anteroposterior Blastema Polarity in Planarian Regeneration. Science, 319, 327-330. [Google Scholar] [CrossRef] [PubMed]
[19] Iglesias, M. (2011) Early Planarian Brain Regeneration Is Independ-ent of Blastema Polarity Mediated by the Wnt/beta-Catenin Pathway. Developmental Biology, 358, 68-78. [Google Scholar] [CrossRef] [PubMed]
[20] Petersen, C.P. and Reddien, P.W. (2009) A Wound-Induced Wnt Expression Program Controls Planarian Regeneration Polarity. Proceedings of the National Academy of Sciences of the United States of America, 106, 17061-17066. [Google Scholar] [CrossRef] [PubMed]
[21] Petersen, C.P. and Reddien, P.W. (2011) Polarized Notum Activa-tion at Wounds Inhibits Wnt Function to Promote Planarian Head Regeneration. Science, 332, 852-855. [Google Scholar] [CrossRef] [PubMed]
[22] Petersen, C.P. and Reddien, P.W. (2009) A Wound-Induced WNT Expression Program Controls Planarian Regeneration Polarity. Proceedings of the National Academy of Sciences of the United States of America, 106, 17061-17066. [Google Scholar] [CrossRef] [PubMed]
[23] Blassberg, R.A., Felix, D.A., Tejada-Romero, B., et al. (2013) PBX/Extradenticle Is Required to Re-Establish Axial Structures and Polarity during Planarian Regeneration. Develop-ment, 140, 730-739. [Google Scholar] [CrossRef] [PubMed]
[24] Chen, C.C., Wang, I. and Reddien, P.W. (2013) pbx Is Required for Pole and Eye Regeneration in Planarians. Development, 140, 719-729. [Google Scholar] [CrossRef] [PubMed]
[25] Morgan, T.H. (1970) Experimental Studies of the Regeneration of Planaria maculata. Rouxs Archives of Developmental Biology, 7, 364-397. [Google Scholar] [CrossRef
[26] Newmark, P.A. and Alvarado, A.S. (2000) Bromodeoxyuri-dine Specifically Labels the Regenerative Stem Cells of planarians. Developmental Biology, 220, 142-153. [Google Scholar] [CrossRef] [PubMed]
[27] Buckingham, M. and Rigby, P.W. (2014) Gene Regulatory Networks and Transcriptional Mechanisms That Control Myogenesis. Developmental Cell, 28, 225-238. [Google Scholar] [CrossRef] [PubMed]
[28] Cutie, S., Hoang, A.T., Payumo, A.Y., et al. (2017) Unconven-tional Functions of Muscles in Planarian Regeneration. Developmental Cell, 43, 657. [Google Scholar] [CrossRef] [PubMed]
[29] Scimone, M.L., Cote, L.E. and Reddien, P.W. (2017) Orthogonal Muscle Fibres Have Different Instructive Roles in Planarian Regeneration. Nature, 551, 623-628. [Google Scholar] [CrossRef] [PubMed]