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Nerve growth factor (NGF) in serum: Evaluation of serum NGF level with a sensitive bioassay employing embryonic sensory neurons
Author(s) -
Stephani U.,
Sutter A.,
Zimmermann A.
Publication year - 1987
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.490170105
Subject(s) - nerve growth factor , bioassay , radioimmunoassay , endocrinology , medicine , in vitro , sensory neuron , chemistry , biology , central nervous system , biochemistry , receptor , genetics
Abstract Considerable controversy surrounds the question of whether or not nerve growth factor (NGF) or a related nerve growth‐promoting factor is present in serum. Recently, supporting its role as a local neuronotrophic factor, the presence of NGF in glial cells and its production in target tissues of NGF‐responsive neurons were demonstrated [Rush: Nature 312:364–367, 1984; Heumann, Korsching, Scott, Thoenen: EMBOJ 3:3183–3189, 1984; Shelton and Reichardt: Proc Natl Acad Sci USA 81:7952–7955, 1984]. At the same time, the concept that NGF may play a role as a humoral factor has been questioned, since careful analyses of serum with specific and sensitive radioimmunoassays [Suda, Barde, Thoenen: Proc Natl Acad Sci USA 75:4042–4046, 1978; Korsching and Thoenen; Proc Natl Acad Sci USA 80:3513–3516, 1983; Furukawa, Kamo, Furukawa, Akazawa, Satoyoshi, Itoh, Hayashi: J Neurochem 40:734–744, 1983] as well as bioassays [Skaper and Varon: Exp Neurol 76:655–665, 1982] have not confirmed earlier reports [Levi‐Montacini and Booker; Proc Natl Acad Sci USA 46:373–391, 1960; Banks, Banthorpe, Charlwood, Pearce, Vernon: Nature 246:503–504, 1973; Hendry: Biochem J 128:1265–1272, 1972] on NGF's representation in serum. In this study serum from mouse, rat, and man was analyzed with an in vitro bioassay system which employs sensory neurons from chicken embyro dorsal root ganglia and which allows the measurement of NGF concentrations as low as 0.8 pM. It was found that sera from all these species contained neuronotrophic activity (S‐NGF). The target cell spectrum as well as characteristic parameters of the neuronal growth response of S‐NGF and of NGF were identical. S‐NGF of mouse serum was completely inhibitable by polyclonal and monoclonal antibodies to mouse submandibular gland β NGF. On polyacrylamide isoelectric focussing gels mouse and human S‐NGF could be recovered from the same position as NGF as well as from the region where α 2 ‐macroglobulin and serum albumin focused. In newborn and adult male and female mice basal S‐NGF levels were equivalent to 10–50 pM NGF. A. fraction of the serum samples of male mice showed elevated S‐NGF levels. The incidence of high S‐NGF levels was more frequent in NMRI and C57BL/6 males than in BALB/c males. Following sialectomy of male mice only basal S‐NGF levels were observed up to 5 weeks after the operation. This indicates that although the submandibular gland may contribute to S‐NGF levels in serum under certain conditions that appeared to be stress related, it cannot be the only source of S‐NGF.