 |
Previous Article | Next Article 
Journal of Neuroscience, Vol 5, 388-407, Copyright © 1985 by Society for Neuroscience
Developmental neural kinship groups in the leech
AP Kramer and DA Weisblat
We have traced the developmental origins of various CNS neurons and glial
cells of a leech to 10 clonally related groups of cells, the bilaterally
paired M, N, O, P, and Q kinship groups. Each kinship group is descended
from one of 10 identifiable blastomeres of the early embryo, the
teloblasts. Of the approximately 200 neurons in each side of a segmental
ganglion, 130 to 160 are in the ipsilateral N, 20 to 50 in the O, 8 to 12
in the P, 6 to 9 in the Q, and 3 to 6 in the M kinship group. A given
identified neuron or glial cell was invariably found to belong to a
particular kinship group, indicating that in leech development neuronal
lineage is highly stereotyped. But cells of related function and morphology
do not necessarily belong to the same neuronal kinship group: of the
mechanosensory neurons, the T and N neurons belong to the N, the Pv neuron
belongs to the P and the PD neuron belongs to the O kinship group.
Similarly, glial cells arise from all four ectodermal teloblasts.
Conversely, neurons within a kinship group are not obviously related in
structure or function: the N kinship group includes sensory, motor, and
effector neurons and interneurons: the O and P kinship groups each include
sensory neurons and interneurons; both the P and Q groups contain
representatives of three distinct morphological classes of interneurons.
Consequently, in early development, the determinants of neuronal identity
in the leech CNS are not segregated in any obvious thematic way in the
cleavages that give rise to the five bilateral pairs of teloblasts. Rather,
the neural kinship groups may be merely the evolutionary vestige of a
primordial distributed nervous system, each quadrant of which was derived
from one teloblast.
This article has been cited by other articles:

|
 |

|
 |
 
S. O. Zhang and D. A. Weisblat
Applications of mRNA injections for analyzing cell lineage and asymmetric cell divisions during segmentation in the leech Helobdella robusta
Development,
May 1, 2005;
132(9):
2103 - 2113.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D.-H. Kuo and M. Shankland
Evolutionary diversification of specification mechanisms within the O/P equivalence group of the leech genus Helobdella
Development,
December 1, 2004;
131(23):
5859 - 5869.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. H. Shain, D. K. Stuart, F. Z. Huang, and D. A. Weisblat
Cell interactions that affect axonogenesis in the leech Theromyzon rude
Development,
September 1, 2004;
131(17):
4143 - 4153.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D.-H. Kuo and M. Shankland
A distinct patterning mechanism of O and P cell fates in the development of the rostral segments of the leech Helobdella robusta: implications for the evolutionary dissociation of developmental pathway and morphological outcome
Development,
January 1, 2004;
131(1):
105 - 115.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. H. Song, F. Z. Huang, G. Y. Chang, and D. A. Weisblat
Expression and function of an even-skipped homolog in the leech Helobdella robusta
Development,
August 1, 2002;
129(15):
3681 - 3692.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Seaver and M Shankland
Establishment of segment polarity in the ectoderm of the leech Helobdella
Development,
January 5, 2001;
128(9):
1629 - 1641.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
D. Shain, D. Stuart, F. Huang, and D. Weisblat
Segmentation of the central nervous system in leech
Development,
January 2, 2000;
127(4):
735 - 744.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
F. Ramirez, C. Wedeen, D. Stuart, D Lans, and D. Weisblat
Identification of a neurogenic sublineage required for CNS segmentation in an Annelid
Development,
January 7, 1995;
121(7):
2091 - 2097.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
D Nardelli-Haefliger, A. Bruce, and M Shankland
An axial domain of HOM/Hox gene expression is formed by morphogenetic alignment of independently specified cell lineages in the leech Helobdella
Development,
January 7, 1994;
120(7):
1839 - 1849.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
D Lans, C. Wedeen, and D. Weisblat
Cell lineage analysis of the expression of an engrailed homolog in leech embryos
Development,
January 3, 1993;
117(3):
857 - 871.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
B. H. NELSON and D. A. WEISBLAT
Conversion of Ectoderm to Mesoderm by Cytoplasmic Extrusion in Leech Embryos
Science,
July 12, 1991;
253(5018):
435 - 438.
[Abstract]
[PDF]
|
 |
|
|