The significance of syncytial tissues for the position of the hexactinellida in the metazoa

被引:30
作者
Leys, SP [1 ]
机构
[1] Univ Alberta, Dept Biol Sci, Edmonton, AB T6G 2E9, Canada
[2] Univ Victoria, Dept Biol, Victoria, BC V8W 3N5, Canada
关键词
D O I
10.1093/icb/43.1.19
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
Hexactinellid sponges are metazoans in which the major tissue component is a multinucleated syncytium. The preferred deepwater habitat of these sponges makes collection of hexactinellids in good condition difficult, and has hindered extensive examination of their body plan. Nonetheless, over the last three decades a number of studies have explored their ecology, histology and physiology. It has been shown that hexactinellids are extremely long-lived animals. Their cytoplasm consists of a giant, multinucleated tissue, the trabecular syncytium, which is connected via open and plugged cytoplasmic bridges to cells such as archaeocytes, choanoblasts, and cells with spherical inclusions. Because all of the sponge is cytoplasmically interconnected, electrical signals can propagate through the animal. The effector response is arrest of the feeding current. The perforate plugged junction apparently allows tissues to specialize in different ways while maintaining limited cytoplasmic continuity. Larvae of hexactinellid sponges are already largely syncytial. Although it is not known when the first syncytial tissues are formed or when perforate plugged junctions first appear during embryogenesis, evidence that embryos are cellular until gastrulation suggests that hexactinellid sponges may have evolved from cellular sponges and that syncytial tissues are not a primitive trait of the Metazoa.
引用
收藏
页码:19 / 27
页数:9
相关论文
共 56 条
[1]   INTERCELLULAR BRIDGES IN SOMATIC-CELLS - CYTOPLASMIC CONTINUITY OF BLASTODERM CELLS OF LOLIGO-PEALEI [J].
ARNOLD, JM .
DIFFERENTIATION, 1974, 2 (06) :335-341
[2]   EVIDENCE FOR MYOSIN MOTORS ON ORGANELLES IN SQUID AXOPLASM [J].
BEARER, EL ;
DEGIORGIS, JA ;
BODNER, RA ;
KAO, AW ;
REESE, TS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (23) :11252-11256
[3]  
BIDDER GP, 1929, ENCYCL BRITANNICA, P254
[4]   Sponge paraphyly and the origin of Metazoa [J].
Borchiellini, C ;
Manuel, M ;
Alivon, E ;
Boury-Esnault, N ;
Vacelet, J ;
Le Parco, Y .
JOURNAL OF EVOLUTIONARY BIOLOGY, 2001, 14 (01) :171-179
[5]   Reproduction of a hexactinellid sponge:: first description of gastrulation by cellular determination in the Porifera [J].
Boury-Esnault, N ;
Efremova, S ;
Bézac, C ;
Vacelet, J .
INVERTEBRATE REPRODUCTION & DEVELOPMENT, 1999, 35 (03) :187-201
[6]  
Carroll SeanB., 2001, DNA DIVERSITY MOL GE
[7]   Sponge phylogeny, animal monophyly, and the origin of the nervous system: 18S rRNA evidence [J].
CavalierSmith, T ;
Chao, EE ;
BouryEsnault, N ;
Vacelet, J .
CANADIAN JOURNAL OF ZOOLOGY, 1996, 74 (11) :2031-2045
[8]   Evaluating multiple alternative hypotheses for the origin of Bilateria: An analysis of 18S rRNA molecular evidence [J].
Collins, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15458-15463
[9]   HOLOCENE SPONGE BIOHERMS ON THE WESTERN CANADIAN CONTINENTAL-SHELF [J].
CONWAY, KW ;
BARRIE, JV ;
AUSTIN, WC ;
LUTERNAUER, JL .
CONTINENTAL SHELF RESEARCH, 1991, 11 (8-10) :771-790
[10]  
Davidson E. H., 2001, Genomic regulatory systems: development and evolution