Development of laminar organization in the mushroom bodies of the cockroach: Kenyon cell proliferation, outgrowth, and maturation

Citation
Sm. Farris et Nj. Strausfeld, Development of laminar organization in the mushroom bodies of the cockroach: Kenyon cell proliferation, outgrowth, and maturation, J COMP NEUR, 439(3), 2001, pp. 331-351
Citations number
89
Categorie Soggetti
Neurosciences & Behavoir
Journal title
JOURNAL OF COMPARATIVE NEUROLOGY
ISSN journal
00219967 → ACNP
Volume
439
Issue
3
Year of publication
2001
Pages
331 - 351
Database
ISI
SICI code
0021-9967(20011022)439:3<331:DOLOIT>2.0.ZU;2-S
Abstract
The mushroom bodies of the insect brain are lobed integration centers made up of tens of thousands of parallel-projecting axons of intrinsic (Kenyon) cells. Most of the axons in the medial and vertical lobes of adult cockroac h mushroom bodies derive from class I Kenyon cells and are organized into r egular, alternating pairs (doublets) of pale and dark laminae. Organization of Kenyon cell axons into the adult pattern of laminae occurs gradually ov er the course of nymphal development. Newly hatched nymphs possess tiny mus hroom bodies with lobes containing a posterior lamina of ingrowing axons, f ollowed by a single doublet, which is flanked anteriorly by a gamma layer c omposed of class II Kenyon cells. Golgi impregnations show that throughout nymphal development, regardless of the number of doublets present, the most posterior lamina serves as the "ingrowth lamina" for axons of newborn Keny on cells. Axons of the ingrowth lamina are taurine- and synaptotagmin-immun onegative. They produce fine growth cone tipped filaments and long perpendi cularly oriented collaterals along their length. The maturation of these Ke nyon cells and the formation of a new lamina are marked by the loss of fila ments and collaterals, as well as the onset of taurine and synaptotagmin ex pression. Class I Kenyon cells thus show plasticity in both morphology and transmitter expression during development. In a hemimetabolous insect such as the cockroach, juvenile stages are morphologically and behaviorally simi lar to the adult. The mush-room bodies of these insects must be functional from hatching onward, while thousands of new neurons are added to the exist ing structure. The observed developmental plasticity may serve as a mechani sm by which extensive postembryonic development of the mushroom bodies can occur without disrupting function. This contrasts with the more evolutionar ily derived holometabolous insects, such as the honey bee and the fruit fly , in which nervous system development is accomplished in a behaviorally sim ple larval stage and a quiescent pupal stage. (C) 2001 Wiley-Liss, Inc.