Identification of the Bursicon-Containing Neurones in Abdominal Ganglia of the Tobacco Hornworm, Manduca Sexta

1982 ◽  
Vol 98 (1) ◽  
pp. 385-401 ◽  
Author(s):  
PAUL H. TAGHERT ◽  
JAMES W. TRUMAN

The abdominal ganglion neurones responsible for the secretion of the peptide hormone bursicon from the transverse nerves of the tobacco hornworm Manduca sexta have been localized. Each unfused abdominal ganglion produced bursicon during adult development. The hormone was then transported to the next posterior transverse nerve for subsequent release following adult emergence. Of the two efferent pathways that connect ganglia to posterior transverse nerves, only one had ultrastructural features consistent with a neurosecretory function. All axons in this pathway contained numerous, elementary, dense-cored granules with diameters ranging from 100 to 300 nm. In pharate adults, cobalt back-filling of this neurosecretory pathway revealed two groups of cell bodies in abdominal ganglia: three dorso-laterally and eight at the mid-line. Hormonal activity was present in lateral regions of the ganglion but not in mid-line regions. In the dorso-lateral region, four blueish cell bodies could be seen in the living tissue. The two combined clusters of four cells from both sides of the ganglion contained more than 60% of the bursicon activity present in the entire ganglion. More careful dissection of the cluster detected the presence of activity in cell pairs and individual members. Individual dye-fills of these blue cells demonstrated that three of these were the three lateral neurones that were back-filled from the transverse nerve. The fourth blue cell may be identical to a neurone whose axon travels in the descending, contralateral connective and exits the nervous system via the next posterior ganglion. On the basis of dendritic geometry, each of the neurones in the bursicon cell cluster could be identified as a unique, individual neurone.

1981 ◽  
Vol 44 (3) ◽  
pp. 302-306 ◽  
Author(s):  
Walter E. Bollenbacher ◽  
Stan L. Smith ◽  
Walter Goodman ◽  
Lawrence I. Gilbert

1987 ◽  
Vol 128 (1) ◽  
pp. 175-192
Author(s):  
W. E. Bollenbacher ◽  
N. A. Granger ◽  
E. J. Katahira ◽  
M. A. O'Brien

A larval moult in the tobacco hornworm, Manduca sexta, involves an endocrine cascade that begins with the release of a cerebral peptide hormone, the prothoracicotropic hormone (PTTH). The release of PTTH is gated, occurs during the scotophase and appears to be developmentally cued. In fourth instar Manduca larvae, PTTH release into the haemolymph occurs as a single burst over a few hours during the head critical period, i.e. the time during which the head (brain) is needed for the initiation of the moult to the fifth (last) instar. Released PTTH activates the prothoracic glands (PGs), and within a few hours the cumulative effect of this event results in a dramatic increase in the haemolymph ecdysteroid titre, which then elicits the moult. An assessment of the capacity of the corpora allata (CA) to synthesize juvenile hormone (JH) in vitro indicates that the above sequence of endocrine events begins only when JH synthesis has reached a nadir for the instar. Since CA activity is an indirect measure of the haemolymph titre of the hormone, it is conceivable that the developmentally cued release of PTTH is permissively controlled by a decreasing haemolymph titre of JH. With the increase in the ecdysteroid titre which marks the end of this endocrine cascade, the CA again become active, presumably to cause the increase in the JH haemolymph titre which directs the larval moult. This investigation has thus established the temporal and quantitative dynamics of the PTTH-PG axis that drive larval moulting and provides insight into the interendocrine regulatory relationships that may exist between the ecdysteroids and JHs. These possible relationships and the role of the brain in their regulation are discussed.


1985 ◽  
Vol 116 (1) ◽  
pp. 395-410 ◽  
Author(s):  
N. J. Tublitz ◽  
J. W. Truman

The abdominal ganglion neurosecretory cells responsible for the synthesis and release of two insect neurohormones, cardioacceleratory peptides 1 and 2 (CAP1 and CAP2), from the perivisceral organs (PVOs) have been identified in the tobacco hawkmoth, Manduca sexta. Previous work established the existence of two groups of abdominal ganglion cell bodies with axons projecting to the PVO: four laterally-situated pairs and five pairs lying on the midline (Taghert & Truman, 1982b). Micro-dissection and bioassay of various parts of an abdominal ganglion revealed that CAP activity was greatest in the medial portion of the ganglion, the portion containing the 10 midline neurones. Six of the 10 midline neurosecretory cells, the new midline bilateral (MB) cells, appeared to differentiate post-embryonically, commencing differentiation late in the last larval instar and reaching maturity midway through adult development. The development of the new MB cells was mirrored by the accumulation of CAP activity in the abdominal nerve cord. Not present in measurable amounts in larvae, CAP activity was first detectable a few days after pupation and reached maximal levels midway through adult development. CAP-like bioactivity was collected from the PVO in response to antidromic stimulation of the nerve containing the new MB axons. No CAP-like bioactivity was detected in those preparations in which the new MB axons were severed or in which other nerves were stimulated. Intracellular stimulation of a new MB neurone evoked the release from the PVO of measurable levels of CAP bioactivity. It was shown that this stimulation-evoked, cardioacceleratory activity was sensitive to protease treatment, and was released only from the cell that was stimulated. On the basis of these experiments, it was concluded that the CAPs are synthesized and secreted from the new MB cells.


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