Ernst-August Seyfarth’s research while affiliated with Goethe University Frankfurt and other places

The ability to maintain human brain explants in tissue culture was a critical step in the use of these cells for the study of central nervous system disorders. Ross G. Harrison (1870–1959) was the first to successfully maintain frog medullary tissue in culture in 1907, but it took another 38 years before successful culture of human brain tissue was accomplished. One of the pioneers in this achievement was Mary Jane Hogue (1883–1962). Hogue was born into a Quaker family in 1883 in West Chester, Pennsylvania, and received her undergraduate degree from Goucher College in Baltimore, Maryland. Research with the developmental biologist Theodor Boveri (1862–1915) in Würzburg, Germany, resulted in her Ph.D. (1909). Hogue transitioned from studying protozoa to the culture of human brain tissue in the 1940s and 1950s, when she was one of the first to culture cells from human fetal, infant, and adult brain explants. We review Hogue’s pioneering contributions to the study of human brain cells in culture, her putative identification of progenitor neuroblast and/or glioblast cells, and her use of the cultures to study the cytopathogenic effects of poliovirus. We also put Hogue’s work in perspective by discussing how other women pioneers in tissue culture influenced Hogue and her research.

The Marine Biological Laboratory (MBL) in Woods Hole, MA provided opportunities for women to conduct research in the late 19th and early 20th century at a time when many barriers existed to their pursuit of a scientific career. One woman who benefited from the welcoming environment at the MBL was Mary Jane Hogue. Her remarkable career as an experimental biologist spanned over 55 years. Hogue was born into a Quaker family in 1883 and received her undergraduate degree from Goucher College. She went to Germany to obtain an advanced degree, and her research at the University of Würzburg with Theodor Boveri resulted in her Ph.D. (1909). Although her research interests included experimental embryology, and the use of tissue culture to study a variety of cell types, she is considered foremost a protozoologist. Her extraordinary demonstration of chromidia (multiple fission) in the life history of a new species of Flabellula associated with diseased oyster beds is as important as it is ignored. We discuss Hogue's career path and her science to highlight the importance of an informal network of teachers, research advisors, and other women scientists at the MBL all of whom contributed to her success as a woman scientist.

In terms of physiology and behavior, Cupiennius salei is one of the best-investigated spider species. However, parts of its anatomy have only been described superficially to date. In the course of a comparative survey of the hemolymph vascular system in Araneae we therefore investigated C. salei using several injection methods in combination with semi-thin sections and micro computer tomography (MicroCT). Like all other Arthropoda, C. salei possesses an open circulatory system. A tubular heart is suspended dorsally in the opisthosoma via a number of ligaments. It is equipped with three pairs of ostia, and three pairs of cardiac arteries. The heart is surrounded by a pericardial sinus in which we were able for the first time to describe an intra-pericardial membrane. Anteriorly, the heart is extended by an anterior aorta which runs through the pedicel and divides into two branches within the prosoma. Arteries emanating from the branches of the aorta supply the prosomal appendages and the central nervous system. The subesophageal ganglion is supplied by numerous fine vessels which emanate from the transganglionic arteries and form tight loops. A network of capillaries, i.e. interconnections between afferent and efferent vessels, is here demonstrated for the first time to exist in the central nervous system of chelicerates. Data are compared with existing literature on the morphology of the circulatory system in Araneae and discussed with regard to the extension of the respiratory system and the varying lifestyles of different spiders.

Here we describe the neuronal organization of the arcuate body in the brain of the wandering spider Cupiennius salei. The internal anatomy of this major brain center is analyzed in detail based on allatostatin-, proctolin-, and crustacean cardioactive peptide (CCAP)-immunohistochemistry. Prominent neuronal features are demonstrated in graphic reconstructions. The stainings revealed that the neuroarchitecture of the arcuate body is characterized by several distinct layers some of which comprise nerve terminals that are organized in columnar, palisade-like arrays. The anatomy of the spider's arcuate body exhibits similarities as well as differences when compared to the central complex in the protocerebrum of the Tetraconata. Arguments for and against a possible homology of the arcuate body of the Chelicerata and the central complex of the Tetraconata and their consequences for the understanding of arthropod brain evolution are discussed.

The tympanal organ of the bushcricket Mecopoda elongata emits pronounced distortion-product otoacoustic emissions (DPOAEs). Their characteristics are comparable to those measured in other insects, such as locusts and moths, with the 2f1-f2 emission being the most prominent one. Yet the site of their generation is still unclear. The spatial separation between the sound receiving spiracle and the hearing organ in this species allows manipulations of the sensory cells without interfering with the acoustical measurements. We tried to interfere with the DPOAE generation by pharmacologically influencing the tympanal organ using the insecticide pymetrozine. The compound appears to act selectively on scolopidia, i.e., the mechanosensor type characteristically constituting tympanal organs. Pymetrozine solutions were applied as closely as possible to the scolopidia via a cuticle opening in the tibia, distally to the organ. Applications of pymetrozine at concentrations between 10(-3) and 10(-7) M to the tympanal organ led to a pronounced and irreversible decrease of the DPOAE amplitudes.

Johann H.L. Flögel (1834-1918) was an amateur scientist and self-taught microscopist in Germany who 130years ago pioneered comparative arthropod neuroanatomy. He was fascinated by innovations in optical instrumentation, and his meticulous studies of the insect supraoesophageal ganglia were the first to use serial sections and photomicrographs to characterize the architecture of circumscribed regions of brain tissue. Flögel recognized the interpretative power resulting from observations across various species, and his comparative study of 1878, in particular, provided a baseline for subsequent workers to evolve a secure nomenclature of insect brain structures. His contributions stand out from contemporary accounts by virtue of their disciplined descriptions and emphasis on identifying comparable elements in different taxa. Here we give a biographical sketch of his life and summarize his remarkable achievements.

Sensitive hearing organs often employ nonlinear mechanical sound processing which generates distortion-product otoacoustic emissions (DPOAE). Such emissions are also recordable from tympanal organs of insects. In vertebrates (including humans), otoacoustic emissions are considered by-products of active sound amplification through specialized sensory receptor cells in the inner ear. Force generated by these cells primarily augments the displacement amplitude of the basilar membrane and thus increases auditory sensitivity. As in vertebrates, the emissions from insect ears are based on nonlinear mechanical properties of the sense organ. Apparently, to achieve maximum sensitivity, convergent evolutionary principles have been realized in the micromechanics of these hearing organs-although vertebrates and insects possess quite different types of receptor cells in their ears. Just as in vertebrates, otoacoustic emissions from insects ears are vulnerable and depend on an intact metabolism, but so far in tympanal organs, it is not clear if auditory nonlinearity is achieved by active motility of the sensory neurons or if passive cellular characteristics cause the nonlinear behavior. In the antennal ears of flies and mosquitoes, however, active vibrations of the flagellum have been demonstrated. Our review concentrates on experiments studying the tympanal organs of grasshoppers and moths; we show that their otoacoustic emissions are produced in a frequency-specific way and can be modified by electrical stimulation of the sensory cells. Even the simple ears of notodontid moths produce distinct emissions, although they have just one auditory neuron. At present it is still uncertain, both in vertebrates and in insects, if the nonlinear amplification so essential for sensitive sound processing is primarily due to motility of the somata of specialized sensory cells or to active movement of their (stereo-)cilia. We anticipate that further experiments with the relatively simple ears of insects will help answer these questions.

Cupiennius salei Keys., a lycosid spider, is night-active in its natural habitat in the highlands of Guatemala. Locomotor activity begins at dusk after several transitional states, each of which is correlated with a particular light level. Actograph measurements in controlled conditions (LD 12:12 or reversed cycles) show that the spiders begin walking immediately after dark. The activity maximum is reached within the first 3 h of the scotophase (though some spiders displayed additional lights-on activity in the first hour of the photophase). In DD, Cupiennius shows an endogenous activity rhythm with a mean period of 24.9 h (± 0.31, SE); typically during the first four to six cycles in DD the rhythm ‘splits’ into two components running at different frequencies. In LL (26 1x) the walking activity became arrhythmic. The results are discussed with reference to field and laboratory observations of Cupiennius behaviour and to the consequences for future physiological research with this species.

We describe here for the first time the development of mechanosensory organs in a chelicerate, the spider Cupiennius salei. It has been shown previously that the number of external sense organs increases with each moult. While stage 1 larvae do not have any external sensory structures, stage 2 larvae show a stereotyped pattern of touch sensitive 'tactile hairs' on their legs. We show that these mechanosensory organs develop during embryogenesis. In contrast to insects, groups of sensory precursors are recruited from the leg epithelium, rather than single sensory organ progenitors. The groups increase by proliferation, and neural cells delaminate from the cluster, which migrate away to occupy a position proximal to the accessory cells of the sense organ. In addition, we describe the development of putative internal sense organs, which do not differentiate until larval stage 2. We show by RNA interference that, similar to Drosophila, proneural genes are responsible for the formation and subtype identity of sensory organs. Furthermore, we demonstrate an additional function for proneural genes in the coordinated invagination and migration of neural cells during sensory organ formation in the spider.

The tympanal hearing organs of insects produce otoacoustic emissions that be recorded with the aid of a sensitive microphone. In vertebrates (including humans), such emissions are considered a by-product of active sound amplification through specialized sensory cells in the inner ear (i.e., the outer hair cells). Force-generation by these cells primarily amplifies faint sound and thus improves auditory sensitivity. As in vertebrates, the emissions from insect ears are based on non-linear mechanical properties of the sense organ. To achieve maximum sensitivity, convergent evolutionary principles were realized in the micromechanics of the ears - although vertebrates and insects possess different types of sensory cells in their auditory organs. Just as in vertebrates, otoacoustic emissions from insects ears depend on an intact metabolism, but so far in tympanal organs, it is not clear if amplification is achieved by active motility of the sensory neurons or if passive cellular characteristics cause the non-linear behavior. In the antennal ears of flies, however, active motility of the flagellum has been demonstrated. Here we review experiments on tympanal organs of grasshoppers and moths; we show that their otoacoustic emissions are produced in a frequency-specific way and can be modified by electrical stimulation of the sensory cells. Even the simple ears of notodontid moths produce distinct emissions, although they have just one auditory neuron. At present it is still uncertain, both for vertebrates and insects, if the non-linear amplification so essential for sensitive sound processing is primarily due to electromotility of the cell body of the sensory cells or to active movement of their hair-bundles or cilium. Further experiments with the relatively simple ears of insects may help to answer these questions.