WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kramer, A. P.
Right arrow Articles by Weisblat, D. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kramer, A. P.
Right arrow Articles by Weisblat, D. A.

 Previous Article  |  Next Article 

Journal of Neuroscience, Vol 5, 388-407, Copyright © 1985 by Society for Neuroscience


ARTICLE

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:


Home page
DevelopmentHome page
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]


Home page
DevelopmentHome page
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]


Home page
DevelopmentHome page
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]


Home page
DevelopmentHome page
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]


Home page
DevelopmentHome page
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]


Home page
DevelopmentHome page
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]


Home page
DevelopmentHome page
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]


Home page
DevelopmentHome page
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]


Home page
DevelopmentHome page
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]


Home page
DevelopmentHome page
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]


Home page
ScienceHome page
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]



-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2010 by Society for Neuroscience ONLINE ISSN: 1529-2401
-