Comparative electron microscopic investigation of the nuchal organs in Protodriloides, Protodrilus, and Saccocirrus (Annelida, Polychaeta)

1990 ◽  
Vol 68 (2) ◽  
pp. 325-338 ◽  
Author(s):  
Günter Purschke

The nuchal organs of the interstitial polychaetes Protodriloides chaetifer, Protodriloides symbioticus, Protodrilus ciliatus, Protodrilus adhaerens, Saccocirrus krusadensis, and Saccocirrus papillocercus were investigated by scanning and transmission electron microscopy. These organs vary from spherical to elongated ciliary brushes and usually lie in shallow pits. In P. symbioticus only a reduced nuchal organ exists, whereas the other species all have well-developed nuchal organs of similar structure consisting of ciliated supportive cells and bipolar primary sensory cells. The perikarya of the sensory cells form the nuchal ganglia, which lie behind the brain. Different retractor muscle cells are attached to the ciliated cells. The number of sensory cells varies from 4 to about 90 according to the size of the nuchal organs. Each sensory cell gives rise to a distal process (dendrite), and 4–25 processes at a time unite to form bundles that penetrate between the ciliated cells. Apically the dendrites terminate in small sensory bulbs, each bearing several microvilli and a modified cilium. The sensory cilia usually branch, lose their axonemes, and extend as microvillus-like structures into the olfactory chamber representing an extracellular space below the reduced cuticle. Specific microvillar processes of the ciliated cells form a dense cover above the cuticle which is only penetrated by the motile cilia of these cells. The ciliated cells are highly pinocytic. The nuchal organs of the species investigated show striking similarities to those of spionids.

Author(s):  
Andrew J. Lovinger ◽  
Bernard Lotz ◽  
Don D. Davis

In contrast to its isotactic isomer, syndiotactic polypropylene has received only little attention. Our main source of understanding of its structure is the X-ray study by Conradini et al., who found the chains to have a (t2g2)2 conformation (corresponding to a 4∗2/1 helix with molecular repeat 0.74 nm), and to be packed in a C-centered unit cell as shown in the left side of Fig. 1. We have recently begun a study of the structure, crystallization, and morphology of syndiotactic polypropylene using electron microscopy and diffraction. Here we concentrate specifically on the electron-diffraction evidence as a function of temperature, in order to obtain an understanding of the evolution and variation of structure in this polymer.Thin films of syndiotactic polypropylene (synthesized by Dr. R. E. Cais as reported previously) were prepared by casting from dilute solution in xylenes at ca. 140°c onto freshly cleaved mica substrates. Following evaporation of the solvent, they were melted and then isothermally crystallized at a variety of temperatures. After shadowing with Pt/C and coating with carbon, they were floated off their substrates for examination by transmission electron microscopy (bright- and dark-field) and selected-area electron diffraction at 100-200 keV.


Author(s):  
A. Márquez ◽  
N.L. Diaz ◽  
H.J. Finol ◽  
M.E. Correa

To date the most accepted definition of sepsis includes the suspicion of infection plus the systemic response to it (tachypnea, tachycardia and hypothermia or hyperthermia). This condition could lead to the so called multiple organ failure syndrome (MOFS) when there are evidences of flinctional compromise in two or more systems. Muscle weakness and wasting are common findings in those patients. The skeletal muscle histopathology in patients with those two conditions has been poorly studied. The only electron microscopic investigation we could find describes alterations in muscle fibers and endplates.In this work we describe the whole spectrum of changes found in skeletal muscle of patients suffering from sepsis and MOFS.Five patients recluded in an Intensive Care Unit were selected, two had a diagnosis of sepsis, and three presented MOFS. Needle muscle biopsies from quadriceps femoris muscle were obtained. Tissue samples were processed with routine techniques for transmission electron microscopy and observed in a Hitachi H-500 electron microscope.


Author(s):  
R. H. Seall ◽  
R. E. Kingsley

It has been shown that the adult mammalian CNS is capable of axonal sprouting and limited regeneration in response to injury, but this regeneration is interrupted by the scar produced in the lesioned area by proliferating glia. Experiments by Barnes and Worrall (1) demonstrated that the proximal stump of a ventral root when grafted to a ganglionectomized dorsal root is capable of reinnervating the spinal cord without interference by the glia, and is capable of forming new functional synapses within the spinal cord. In an effort to provide anatomical verification for this physiological study, we repeated their experimental procedure. A transmission electron microscopic investigation of the spinal cord where the dorsal roots terminate was undertaken in an attempt to identify these reinnervating axons and newly formed synapses. Regeneration time was varied from 8 to 16 weeks. In order to identify reinnervating from normal tissue, the graft was lesioned 3 or 4 days prior to preparation of the spinal cord for electron microscopy.


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