Literature DB >> 12353295

Novel bridge of axon-like processes of epithelial cells in the aboral sense organ of ctenophores.

Sidney L Tamm1, Signhild Tamm.   

Abstract

We describe by light and electron microscopy a novel structure in the aboral sense organ (apical organ) of cydippid (Pleurobrachia) and lobate (Mnemiopsis) ctenophores. An elevated bundle of long, thin, microtubule-filled processes arises from the apical ends of two groups of epithelial cells located on opposite sides of the apical organ along the tentacular plane of the body. This bundle of axon-like processes arches over the epithelial floor like a bridge, with branches at both ends running toward opposing pairs of ciliary balancers that are motile pacemakers for the rows of locomotory ciliary comb plates. The bridge in Pleurobrachia is approximately 40 microm long and 3-4 microm wide and consists of approximately 60 closely packed processes, 0.2-0.8 microm thick, containing vesicles and numerous microtubules running parallel to their long axes. There are approximately 30 epithelial cells in each of the two groups giving rise to the bridge and each cell forms a single process, so roughly half of the processes in the bridge must originate from cells on one side and diverge into branches to a pair of balancers on the opposite side of the apical organ. The 150-200 cilia in each balancer arise from morphologically complex cellular projections with asymmetric lateral extensions directed towards a fork of the bridge. Presynaptic triad structures and vesicles are found in this region but clear examples of synaptic contacts between bridge processes and balancer cells have not yet been traced. Cydippid larvae of Mnemiopsis have a conspicuous bridge along the tentacular plane of the apical organ. Beroid ctenophores that lack tentacles at all stages do not have a bridge. We discuss the possibility that the bridge is an electrical conduction pathway to balancers that coordinates tentacle-evoked swimming responses of ctenophores, such as global ciliary excitation. Copyright 2002 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2002        PMID: 12353295     DOI: 10.1002/jmor.10019

Source DB:  PubMed          Journal:  J Morphol        ISSN: 0022-2887            Impact factor:   1.804


  5 in total

1.  Diversity of cilia-based mechanosensory systems and their functions in marine animal behaviour.

Authors:  Luis Alberto Bezares-Calderón; Jürgen Berger; Gáspár Jékely
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2019-12-30       Impact factor: 6.237

Review 2.  Convergent evolution of neural systems in ctenophores.

Authors:  Leonid L Moroz
Journal:  J Exp Biol       Date:  2015-02-15       Impact factor: 3.312

3.  Developmental expression of homeobox genes in the ctenophore Mnemiopsis leidyi.

Authors:  Kevin Pang; Mark Q Martindale
Journal:  Dev Genes Evol       Date:  2008-05-27       Impact factor: 2.116

4.  Lim homeobox genes in the Ctenophore Mnemiopsis leidyi: the evolution of neural cell type specification.

Authors:  David K Simmons; Kevin Pang; Mark Q Martindale
Journal:  Evodevo       Date:  2012-01-13       Impact factor: 2.250

5.  Reafference and the origin of the self in early nervous system evolution.

Authors:  Gáspár Jékely; Peter Godfrey-Smith; Fred Keijzer
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2021-02-08       Impact factor: 6.237

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.