Ruben Adler

Trophic and Specifying Factors Directed to Neuronal Cells

Publisher Summary This chapter examines the effects of trophic and specifying factors directed to neuronal cells. Neurons are living cells and not just the transport of information communication; their value to the network may be only as good as their functional state at any given time. Also, they are subject to extrinsic influences from their own environment.The development of a nervous system involves various processes: (1) neuronal cell death, (2) neuritic elongation and guidance, and (3) establishment of transmitter functions. CNS tissues comprise a large variety of neuronal subsets. The subset being considered the target for a given factor must remain present in dissociate and subsequent culture. In turn, this requirement demands its independent identification by morphological or biochemical markers, which will also serve to monitor survival, neurite, and even transmitter responses to the putative factors. Thereafter, trophic influences are those directed to the quantitative regulation of the anabolic machinery of the cell. Hence, trophic influences can be equally responsible for decline and death (inadequate trophic supply), survival and maintenance (moderate trophic input), or overproduction (high trophic drive). Specifying influences, on the other hand, provide qualitative instructions to the cells and define which particular cell behaviors are to benefit from the same (high) trophic drive.

Cholinergic neuronotrophic factors: I. Survival, neurite outgrowth and choline acetyltransferase activity in monolayer cultures from chick embryo ciliary ganglia

Two key components of neural development and regeneration, survival of the involved neurons and elongation of neuritic elements, are likely to depend on the availability of an appropriate trophic drive to these neurons. At present, only one trophic factor, Nerve Growth Factor, is known to ensure both survival and neuritic growth for its target neurons. A search for a second such agent, a putative cholinergic neuronotrophic factor (CNTF), has been undertaken using as indicators neuronal survival, neurite outgrowth and choline acetyltransferase (CAT) activity in monolayer cell cultures. Eight-day chick embryo ciliary ganglia yielded two monolayer culture systems which appear to be well suited for a CNTF assay. Ciliary ganglionic dissociates, seeded on a highly adhesive collagen substratum, show no neuronal survival by 24 h if the medium is supplemented only with serum or chick embryo extract. However serum and embryo extract combined support survival of, and extensive neuritic outgrowth from, nearly the theoretical number of ganglionic neurons seeded. Alternatively, ciliary ganglionic neurons can be made to survive and produce a profuse neuritic outgrowth on polyornithine-coated dishes if supplied with medium conditioned over chick embryo heart muscle cultures, as already described by other laboratories. The two trophic sources differ markedly in their effects on the ganglionic neurons when tested on collagen or polyornithine substrata, and in some cases when different serum supplements are used. Neuronal survival, neurite production and, possibly, CAT activity appear to be subject to independent regulation. The culture systems used in this study can be developed into quantitative bioassays for the isolation of the different agents responsible for neuronal survival and neurite promotion, and for the investigation of their activities.

chapter 6 Nerve Growth Factors and Control of Nerve Growth

Publisher Summary This chapter surveys developmental observations indicating the occurrence of target derived signals that permit a neuron to survive at and beyond a critical time in its life course. It introduces and illustrates the concepts of a trophic drive responsible for both survival and growth supportive production, and of specifying influences that signal the cell to proceed (or do away) with selected performances. With that conceptual background, the chapter examines, in detail, two examples of factors directed toward neurons. The first is a group of target-derived agents recently shown to promote survival and/or neurite growth in cultured ciliary neurons. The second is the classic nerve growth factor, including the mechanisms through which it may exercise its trophic functions of sensory and sympathetic neurons. The chapter also explores some signals and mechanisms for neurite growth. It discusses whether the concepts regarding the regulation of older cells apply during earlier phases of their life, before they connect with their target or even acquire a postmitotic neuronal identity.

Development, reactivity and GFA immunofluorescence of astroglia-containing monolayer cultures from rat cerebrum

SummaryThis report describes detailed protocols for the dissociation, seeding and growthin vitro of monolayer cultures derived from neonatal rat cerebrum. Primary cultures derived by using different seeding densities andin vitro ages were examined qualitatively and quantitatively for morphological composition in terms of two major cell classes (flat cells and process-bearing cells) and for the presence within these classes of glial fibrillary acidic protein (GFA) as detected by immunofluorescence histochemistry. Also examined was the reaction of the cells to serum withdrawal plus the administration of dibutyryl cyclic AMP in terms of the conversion of flat cells into process-bearing cells. Conditions are defined for the generation ofin vitro cell populations, more than 90% of which are GFA-containing flat cells which can all be experimentally converted into cells with processes. These well-defined culture preparations will serve as useful models for future studies of astroglial behaviour.

The bZIP transcription factor Nrl stimulates rhodopsin promoter activity in primary retinal cell cultures.

In vitro DNA binding assays and transient transfection analysis with monkey kidney cells have implicated Nrl, a member of the Maf-Nrl subfamily of bZIP transcription factors, and the Nrl response element (NRE) in the regulation of rhodopsin expression. We have now further explored the role of the NRE and surrounding promoter elements. Using the yeast one-hybrid screen with integrated NRE and flanking DNA as bait, the predominant clone obtained was bovine Nrl. Recovery of truncated clones in the screen demonstrated that the carboxyl-terminal half of Nrl, which contains the basic and leucine zipper domains, is sufficient for DNA binding. To functionally dissect the rhodopsin promoter, transient expression studies with primary chick retinal cell cultures were performed. Deletion and mutation analyses identified two positive regulatory sequences: one between −40 and −84 base pairs (bp) and another between −84 and −130 bp. Activity of the −40 to −84 region was shown to be largely due to the NRE. On co-transfection with an NRL expression vector, there were 3-5-fold increases in the activity of rhodopsin promoter constructs containing an intact NRE but little or no effect with rhodopsin promoters containing a mutated or deleted NRE. Nrl was more effective than the related bZIP proteins, c-Fos and c-Jun, in stimulating rhodopsin promoter activity. The −84- to −130-bp region acted synergistically with the NRE to enhance both the level of basal expression and the degree of Nrl-mediated trans-activation. These studies support Nrl as a regulator of rhodopsin expression in vivo, identify an additional regulatory region just upstream of the NRE, and demonstrate the utility of primary retinal cell cultures for characterizing both the cis-acting response elements and trans-acting factors that regulate photoreceptor gene expression.

Polyornithine-attached neurite-promoting factors (PNPFs). Culture sources and responsive neurons

We have recently reported the existence within chick embryo heart cell conditioned medium (HCM) of two distinct and independently assayable factors. One agent, ciliary neuronotrophic factor (CNTF), supports the in vitro survival of 8-day chick embryo ciliary ganglionic (CG) neurons. The other factor, polyornithine-attachable neurite promoting factor (PNPF) is required for extensive neuritic growth from these same CNTF-supported CG neurons. In the present study we have examined the occurrence of PNPF activity within nearly 100 different conditioned media using our previously described chick CG bioassay system. From this screening we conclude that: (1) PNPF production is a rather widespread property of cultured neural as well as non-neural cells; and (2) the chick bioassay is sensitive to PNPF activity from all the species examined, including mouse, rat, human and chick cells. We next examined the effects of 3 representative PNPF-containing conditioned media (from chick heart, mouse Schwann and rat Schwannoma) on neurite production from 3 other peripheral ganglionic neuronal cultures (8-day chick dorsal root, 11-day chick sympathetic, and neonatal mouse dorsal root ganglia) as well as 4 central neuronal cultures (8-day chick embryo telencephalon, optic lobe and spinal cord and neonatal mouse cerebellum). The results of these studies indicate: (1) that the peripheral neurons exhibit a dramatic increase in neurite production in response to PNPF which can be easily recognized both qualitatively and quantitatively; whereas (2) the CNS neurons showed essentially no PNPF-induced increase in neurite production. The sole exception to the latter was the appearance within the chick spinal cord cultures of a neuronal population which extended very long neurites in response to PNPF.

Cholinergic Neuronotrophic Factors: Fractionation Properties of an Extract from Selected Chick Embryonic Eye Tissues

Abstract: An aqueous extract derived from selected intraocular tissues of 15‐day chick embryos contains a soluble macromolecular agent which is capable of ensuring the survival of 8‐day chick embryonic ciliary ganglionic neurons in monolayer culture. When this ciliary neuronotrophic factor (CNTF) was concentrated using ultrafiltration and subjected to Sephadex G100 and G200 chromatography, activity was detected in most of the eluted fractions. A peak of the most active fractions was eluted in a region corresponding to a molecular weight of 35–40 ± 103 and contained about 20‐30% of the applied protein. CNTF activity bound readily to DE‐52 cellulose resin at neutral pH and was eluted with NaCl in a narrow region containing about 20‐40% of the applied protein. Gel electrophoretic staining profiles of the active DE52 fraction indicated considerable (but still only partial) simplification in protein composition. While significant CNTF activity losses were incurred in response to each of the above treatments, an active material could be conveniently generated in one working day in milligram amounts having a specific activity of 60,000 trophic units/mg protein. This trophic activity is in the same range as that of the only other known neuronotrophic factor, Nerve Growth Factor.

Cholinergic neuronotrophic factors: V. Segregation of survival- and neurite-promoting activities in heart-conditioned media

Chick embryo ciliary ganglionic (CG) neurons will not survive in monolayer culture unless special supplements are provided in the medium. We have previously reported that two such supplements, chick embryo extract and medium conditioned over chick heart cell cultures (HCM) share the capacity to support survival of CG neurons but differ in their neurite-promoting effects. Thus, embryo extract elicited neuritic outgrowth only on collagen and HCM did so only on polyornithine (PORN), although both agents supported neuronal survival on both substrata. We report here the separation and quantitation of two different HCM components. One is a trophic agent which supports survival of CG neurons on either collagen or PORN, but does not seem to adsorb to either substratum. The other is a neurite-promoting factor (NPF) which adsorbs to PORN but not to collagen. Overnight incubation of HCM on PORN yields two products: (i) an NPF-deprived HCM, that has no neurite-promoting activity and (ii) an NPF-coated PORN, that promotes neuritic development of CG neurons trophically supported by either embryo extract or NPF-deprived HCM. CG requirements for neuritic outgrowth were also examined in explant cultures. No neurites were present after 24 h when explants were cultured in plain medium on PORN. Very extensive radial neuritic outgrowth was observed when explants were cultured in HCM on fresh PORN, or in NPF-deprived HCM on NPF-derivatized PORN. In contrast to what happens with dissociated cells, neuritic outgrowth was also present when ganglia were cultured in NPF-deprived HCM on fresh PORN. However, neurites grew radially only to a limited extent, after which they adopted a circular pattern grossly concentric to the ganglionic explant. It is proposed that explanted ciliary ganglia produce a neurite-promoting factor that coats the PORN substratum in widening circles.

Neurite‐Promoting Factor in Conditioned Medium from RN22 Schwannoma Cultures: Bioassay, Fractionation, and Properties

Abstract: On polyornithine (PORN) substrata dissociated 8‐day chick embryo ciliary ganglionic neurons will survive if the culture medium is supplemented with Ciliary Neuronotrophic Factor. However, neuritic growth will not occur unless the substratum is derivatized with a PORN‐bindable Neurite Promoting Factor (PNPF). In this preliminary study we report that soluble PNPF can be (1) assayed by a convenient in vitro system; (2) obtained in relatively large amounts from serum‐free media conditioned over RN22 Schwannoma cultures; (3) concentrated by using Amicon XM100 ultrafiltration; and (4) separated from nearly all of the non‐active protein by using ion‐exchange chromatography. The partially purified PNPF can be concentrated using XM100 and is heat‐ and protease‐sensitive. In the course of these fractionation studies we observed in some cases a concentration‐dependent interference with the expression of PNPF activity in the bioassay; we propose graphical methods to permit the simultaneous determination of PNPF and the extent of such interference. Different treatments that affected the interference property did not always affect PNPF activity in a reciprocal manner, leaving open the possibility that the interference with PNPF activity results from reversible alteration of the PNPF molecule, or that there exists a separate interfering agent.

Cholinergic neuronotrophic factors: III. Developmental increase of trophic activity for chick embryo ciliary ganglion neurons in their intraocular target tissues

Abstract Between stages 34 and 40 in the chick embryo, the ciliary ganglion (CG) undergoes a 50% loss of neurons. Such neuronal death is a common feature in neural development and it has been proposed that neurons are dependent for survival on trophic support from their target tissues. Using an in vitro bioassay it was previously shown in this laboratory that trophic activity for CG neurons is highly concentrated in eye structures containing CG target tissues. In the present study we have found that trophic activity in the eye increases markedly between stages 37 and 39, the time when neuronal death in the ciliary ganglion is ending. Thus, a developmental increase in trophic activity within the eye may be involved in determining neuronal survival in the CG. Furthermore, this study provides the first indication that the trophic content of target tissue is itself developmentally regulated.