Intercalary regeneration in planarians

How can a planarian regenerate its entire body from a small portion of its body? Neoblasts, the totipotent stem cells of planarian, are assumed to be able to produce all missing cell types. However, we do not know how the cell fate of these cells is controlled during regeneration. Our recent studies with molecular markers suggest that intercalary regeneration is the fundamental principle in planarian regeneration. Here, we introduce the intercalation induced by ectopic grafting along the anteroposterior (A‐P), dorsoventral (D‐V), and left–right (L‐R) axes. Blastema formation is evoked by ectopic D‐V interactions after wound closure. Intercalation between the blastema and stump induces rearrangement of the positional identities along the A‐P axis. Consequently, totipotent stem cells change their differentiation patterns according to the newly rearranged positional identities along the A‐P, D‐V, and L‐R axes. According to the classic view, the blastema is regarded as the place where undifferentiated cells accumulate and regenerative events occur. Here, we propose a new interpretation, i.e., that the blastema may work as a signaling center inducing intercalary regeneration. Also, the roles of molecules and genes involved in intercalary regeneration are discussed. Developmental Dynamics 226:308–316, 2003. © 2003 Wiley‐Liss, Inc.

[1]  T. H. Morgan,et al.  Experimental studies of the regeneration of Planaria maculata , 2015, Roux's archives of developmental biology.

[2]  Kiyokazu Agata,et al.  Mediolateral intercalation in planarians revealed by grafting experiments , 2003, Developmental dynamics : an official publication of the American Association of Anatomists.

[3]  Kazuho Ikeo,et al.  FGFR-related gene nou-darake restricts brain tissues to the head region of planarians , 2002, Nature.

[4]  T. Gojobori,et al.  Induction of a noggin-like gene by ectopic DV interaction during planarian regeneration. , 2002, Developmental biology.

[5]  T. Gojobori,et al.  The expression of neural-specific genes reveals the structural and molecular complexity of the planarian central nervous system , 2002, Mechanisms of Development.

[6]  Tetsutaro Hayashi,et al.  Planarian fibroblast growth factor receptor homologs expressed in stem cells and cephalic ganglions , 2002, Development, growth & differentiation.

[7]  J. Baguñá,et al.  Regeneration in planarians and other worms: New findings, new tools, and new perspectives. , 2002, The Journal of experimental zoology.

[8]  T. Gojobori,et al.  Dissecting planarian central nervous system regeneration by the expression of neural‐specific genes , 2002, Development, growth & differentiation.

[9]  Phillip A. Newmark,et al.  Not your father's planarian: a classic model enters the era of functional genomics , 2002, Nature Reviews Genetics.

[10]  K. Watanabe,et al.  Dorsal and ventral positional cues required for the onset of planarian regeneration may reside in differentiated cells. , 2001, Developmental biology.

[11]  K. Watanabe,et al.  Planaria FoxA (HNF3) homologue is specifically expressed in the pharynx-forming cells. , 2000, Gene.

[12]  A. Salvetti,et al.  An MCM2‐related gene is expressed in proliferating cells of intact and regenerating planarians , 2000, Developmental dynamics : an official publication of the American Association of Anatomists.

[13]  A. Sánchez Alvarado,et al.  Bromodeoxyuridine specifically labels the regenerative stem cells of planarians. , 2000, Developmental biology.

[14]  K. Watanabe,et al.  Organization and Regeneration Ability of Spontaneous Supernumerary Eyes in Planarians —Eye Regeneration Field and Pathway Selection by Optic Nerves— , 2000, Zoological science.

[15]  Kiyokazu Agata,et al.  Ectopic pharynxes arise by regional reorganization after anterior/posterior chimera in planarians , 1999, Mechanisms of Development.

[16]  K. Agata,et al.  Molecular and cellular aspects of planarian regeneration. , 1999, Seminars in cell & developmental biology.

[17]  T. Gojobori,et al.  Neural network in planarian revealed by an antibody against planarian synaptotagmin homologue. , 1999, Biochemical and biophysical research communications.

[18]  K. Watanabe,et al.  The process of pharynx regeneration in planarians. , 1999, Developmental biology.

[19]  K. Watanabe,et al.  The planarian HOM/HOX homeobox genes (Plox) expressed along the anteroposterior axis. , 1999, Developmental biology.

[20]  G. Schoenwolf,et al.  Reconstitution of the organizer is both sufficient and required to re-establish a fully patterned body plan in avian embryos. , 1999, Development.

[21]  K. Watanabe,et al.  The role of dorsoventral interaction in the onset of planarian regeneration. , 1999, Development.

[22]  K. Watanabe,et al.  Expression of vasa(vas)-related genes in germline cells and totipotent somatic stem cells of planarians. , 1999, Developmental biology.

[23]  K. Agata,et al.  Identification of Two Distinct Muscles in the Planarian Dugesia japonica by their Expression of Myosin Heavy Chain Genes , 1998 .

[24]  Kentaro Kato,et al.  Molecular Cloning of Bone Morphogenetic Protein (BMP) Gene from the Planarian Dugesia japonica , 1998 .

[25]  A. Matsuno,et al.  Ultrastructural Studies of Calcium Location during the “Catch” Contraction of Clam Smooth Adductor Muscle Cells , 1998 .

[26]  K. Watanabe,et al.  Identification of a receptor tyrosine kinase involved in germ cell differentiation in planarians. , 1998, Biochemical and biophysical research communications.

[27]  K. Watanabe,et al.  Structure of the Planarian Central Nervous System (CNS) Revealed by Neuronal Cell Markers , 1998, Zoological science.

[28]  K. Agata,et al.  A planarian orthopedia homolog is specifically expressed in the branch region of both the mature and regenerating brain , 1997, Development, growth & differentiation.

[29]  G. Campbell,et al.  Initiation of the proximodistal axis in insect legs , 1995, Development.

[30]  I. Hori Role of fixed parenchyma cells in blastema formation of the planarian Dugesia japonica. , 1991, The International journal of developmental biology.

[31]  S. Bryant,et al.  Supernumerary limgs in amphibians: experimental production in Notophthalmus viridescens and a new interpretation of their formation. , 1976, Developmental biology.

[32]  V. French Leg regeneration in the cockroach, Blatella germanica. II. Regeneration from a non-congruent tibial graft/host junction. , 1976, Journal of embryology and experimental morphology.

[33]  S. Bryant,et al.  The interaction between the blastema and stump in the establishment of the anterior--posterior and proximal--distal organization of the limb regenerate. , 1975, Developmental biology.

[34]  T. Kido Studies on the Pharynx Regeneration in Phanarian,Dugesia gonocephala I.Historogical Observation in the Transected Pieces , 1961 .

[35]  T. Kido Studies on the pharynx regeneration in planarian,Dugesia gonocephala,1,2. , 1961 .

[36]  K. Agata,et al.  Distinct structural domains in the planarian brain defined by the expression of evolutionarily conserved homeobox genes , 1999, Development Genes and Evolution.

[37]  L. Riddiford,et al.  Juvenile hormone modulates 20-hydroxyecdysone-inducible ecdysone receptor and ultraspiracle gene expression in the tobacco hornworm, Manduca sexta , 1999, Development Genes and Evolution.

[38]  J. Bayascas,et al.  Planarian Hox genes: novel patterns of expression during regeneration. , 1997, Development.

[39]  L Wolpert,et al.  Positional information and pattern formation in development. , 1994, Developmental genetics.

[40]  J. Baguñá Mitosis in the intact and regenerating planarian Dugesia mediterranea n.sp. II. Mitotic studies during regeneration, and a possible mechanism of blastema formation , 1976 .

[41]  J. Baguñá Mitosis in the intact and regenerating planarian Dugesia mediterranea n.sp. I. Mitotic studies during growth, feeding and starvation , 1976 .