Hostname: page-component-cd9895bd7-mkpzs Total loading time: 0 Render date: 2024-12-19T18:09:53.608Z Has data issue: false hasContentIssue false

Participation of nerve growth factor in the regulation of ovarian function

Published online by Cambridge University Press:  26 September 2008

Gregory A Dissen*
Affiliation:
Divison of Neuroscience, Oregon Regional Primate Reserch Center/Oregon Health Sciences University, Portland, Oregon, USA.
Artur Mayerhofer
Affiliation:
Divison of Neuroscience, Oregon Regional Primate Reserch Center/Oregon Health Sciences University, Portland, Oregon, USA.
Sergio R. Ojeda
Affiliation:
Divison of Neuroscience, Oregon Regional Primate Reserch Center/Oregon Health Sciences University, Portland, Oregon, USA.
*
G.A. Dissen, Division of Neuroscience, Oregon science, Oregon Regional Primate Research Center/Oregon Health Sciences University, 505 N.W. 185th Avenue, Portland, OR 97006-3499, USA.

Extract

Nerve growth factor (NGF) belongs to a family of related target-derived proteins required for the survival and development of discrete neuronal populations in the central and peripheral nervous systems (Levi-Montalcini, 1987; Snider, 1994). Although initial observations led to the conclusion that the biological actions of neurotrophins are restricted to the nervous system (Thoenen, 1991; Raffioni et al. 1993), new evidence suggests that they, and in particular NGF, can also affect non-neuronal cells.

Type
Article
Copyright
Copyright © Cambridge University Press 1996

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Amsterdam, A.. Rotmensch, S.. (1987). Structure–function relationships during granulosa cell differentiation. Endocr. Rev. 8, 309–37.CrossRefGoogle ScholarPubMed
Barbacid, M.. Lamballe, F.. Pulido, D.. Klein, R.. (1991). The trk family of tyrosine protein kinase receptors. Biochim. Biophys. Ada. 1072, 115–27.Google Scholar
Benedetti, M.. Levi, A.. Chao, M.V.. (1993). Differential expression of nerve growth factor receptors leads to altered binding affinity and neurotrophin responsiveness. Proc. Natl. Acad. Sci. USA. 90, 7859–63.CrossRefGoogle ScholarPubMed
Bennett, M.V.L.. Barrio, L.C.. Bargiello, T.A.. Spray, D.C.. Hertzberg, E.. Siez, J.C.. (1991). Gap junctions: new tools, new answers, new questions. Neuron. 6, 305–20.CrossRefGoogle ScholarPubMed
Beyer, E.C.. Paul, D.L.. Goodenough, D.A.. (1987). Connexin 43: a protein from rat heart homologous to gap junction protein from liver. I. Cell Biol. 105, 2621–29.CrossRefGoogle Scholar
Bjersing, L.. Cajander, S.. (1974). Ovulation and the mechanism of follicle rupture. Cell Tissue Res. 153, 15–30.CrossRefGoogle ScholarPubMed
Carter, B.D., Kaltschmidt, C., Kaltschmidt, B., Offenhäuser, N., Böhm-Matthaei, R, Baeuerle, P.A.. Barde, Y.-A.. (1996). Selective activation of NF-kB by nerve growth factor through the neurotrophin receptor p75. Science. 272, 542–5.CrossRefGoogle ScholarPubMed
Cordon-Cardo, C, Tapley, P., Jing, S., Nanduri, V., O'Rourke, E., Lamballe, F., Kovary, K., Jones, K., Reichardt, L.F., Barbacid, M.. (1991). The trk tyrosine protein kinase mediates the mitogenic properties of nerve growth factor and neurotrophin-3. Cell. 66, 173–83.CrossRefGoogle ScholarPubMed
Curry, T.E. Jr. Dean, D.D.. Sanders, S.L., Pedigo, N.G., & Jones, P.B.C.. (1989). The role of ovarian proteases and their inhibitors in ovulation. Steroids. 54 501–21.CrossRefGoogle ScholarPubMed
Curry, T.E. Jr Mann, J.S., Estes, R.S., Jones, P.B.C.. (1990). α–Macroglobulin and tissue inhibitor of metalloprotein-ases: collagenase inhibitors in human preovulatory ovaries. Endocrinology. 127, 63–8.CrossRefGoogle Scholar
Dekel, N.. (1988). Regulation of oocyte maturation by cell to cell communication. In Cell to Cell Communication in Endocrinology, ed. F., Piva, C.W., Bardin, G., Forti & M, Motta, 181–94. New York: Raven Press.Google Scholar
Dermitzel, R., Spray, D.C.. (1993). Gap junctions in the brain: where, what type, how many and why?. Trends Neurosci. 16 186–92.CrossRefGoogle Scholar
Dissen, G.A., Hill, D.F., Costa, M.E., Dees, W.L., Lara, H.E., & Ojeda, S.R.. (1996a). A role for trkA nerve growth factor receptors in mammalian ovulation. Endocrinology. 137, 198209.CrossRefGoogle ScholarPubMed
Dissen, G.A.. Mayerhofer, A.. Parrot, J.A.. Hill, D.F.. Skinner, M.K. & Ojeda, S.R.. (1996b). Neurotrophins and ovarian function: activation of trkA receptors causes periovulatory-like changes in thecal cell activity. In Proceeding of the Tenth International Congress on Endocrinology., pp. 578 (abstract)Google Scholar
Erickson, G.F., Magoffin, D.A., Dyer, C.A.. & Hofeditz, C.. (1985). The ovarian androgen producing cells: a review of structure/function relationships. Endocr. Rev. 6, 371–99.CrossRefGoogle Scholar
Espey, L.L.. & Lipner, H.. (1994). Ovulation. In Physiology of Reproduction, 2nd edn, ed E, Knodil & JD, Neill, pp. 725–80. New York: Ravan PressGoogle ScholarPubMed
Granot, I., Dekel, N.. (1994). Phosphorylation and expression of connexin-43 ovarian gap junction protein are regulated by luteinising hormone. J. Biol. Chem. 269, 30502–9.CrossRefGoogle Scholar
Hantzopoulos, P.A.. Suri, C., Glass, D.J., Goldfard, M.P.. Yancopoulos, G.D.. (1994). The low affinity NGF receptor, p75, can collaborate with each of the trks to potentiate functional responses to the neurotrophins. Neuron. 13, 187201.CrossRefGoogle Scholar
Kaplan, D.R., Hempstead, B.L., Martin-Zanca, D., Chao, M.V., Parada, L.F.. (1991a). The trk proto-oncogene product: a signal transducing receptor for nerve growth factor. Science. 252, 554–8.CrossRefGoogle ScholarPubMed
Kaplan, D.R., Martin-Zanca, D., Parada, L.F.. (1991b). Tyrosine phosphorylation and tyrosine kinase activity of trk proto-oncogene product induced by NGF. Nature. 350, 158–60.CrossRefGoogle ScholarPubMed
Kim, U.H., Fink, D. Jr. Kim, H.S., Park, D.J., Contreras, M.L., Guroff, G., Rhee, S.C.. (1991). Nerve growth factor stimulates phosphorylation of phospholipase C-gamma in PC12 cells. J. Biol. Chem. 266, 1359–62.CrossRefGoogle ScholarPubMed
Klein, R., Jing, S., Nanduri, V., O'Rourke, E., Barbacid, M.. (1991). The trk proto-oncogene encodes a receptor for nerve growth factor. Cell. 65, 189–97.CrossRefGoogle ScholarPubMed
Lau, A.F., Kanemitsu, M.Y., Kurata, W.E., Danesh, S., Boynton, A.L.. (1992). Epidermal growth factor disrupts gap–junctional communication and induces phosphorylation of connexin 43 on serine. Mo. Biol. Cell. 3, 865–74.CrossRefGoogle Scholar
Levi-Montalcini, R.. (1987). The nerve growth factor 35 years later. Science. 237, 1154–62.CrossRefGoogle ScholarPubMed
Martin-Zanca, D.. Oskam, R., Mitra, G.. Copeland, T. & Barbacid, M.. (1989). Molecular and biochemical characterization of the human trk proto-oncogene. Mol. Cell. Biol. 9, 2433.Google ScholarPubMed
Mayerhofer, A., Garfield, R.E.. (1995). Immunocytochemical analysis of the expression of gap junction protein connexin 43 in the rat ovary. Mol. Reprod. Dev. 41 331–38.CrossRefGoogle ScholarPubMed
Mayerhofer, A., Dissen, G.A., Parrott, J.A., Hill, D.F., Mayer-hofer, D., Garfield, R.E., Costa, M.E., Skinner, M.K.. & Ojeda, S.R.. (1996). Involvement of nerve growth factor in the ovulatory cascade: trkA receptor activation inhibits gap–junctional communication between thecal cells. Endocrinology. 137, 5662.CrossRefGoogle ScholarPubMed
Meakin, S.O., Shooter, E.M.. (1992). The nerve growth factor family of receptors. Trends Neurosci. Edocrinology. 133, 323–31.Google Scholar
Ohmichi, M., Decker, S.J., Pang, L.. & Saltiel, A.R. (1991). Nerve growth factor binds to the 140 kd trk proto-oncogene product and stimulates its association with the src homology domain of phospholipase Cγ.Biochem. Biophys. Rev. Commun. 179, 217–23.CrossRefGoogle Scholar
Raffioni, S., Bradshaw, R.A., Buxser, S.E.. (1993). The receptors for nerve growth factor and other neurotrophins. Annu. Rev. Biochem. 62, 823–50.CrossRefGoogle ScholarPubMed
Reich, R.. Daphna-Iken, D.., Chun, S.Y., Popliker, M., Slager, R., Adelman-Grill, B.C.. Tsafriri, A.. (1991). Preovulatory changes in ovarian expression of collagenases and tissue metalloproteinase inhibitor messenger ribonucleic acid: role of eicosanoids. Endocrinology. 129, 1869–75.CrossRefGoogle ScholarPubMed
Risek, B., Guthrie, S., Kumar, N., Gilula, N.B.. (1990). Modulation of gap junction transcript and protein expression during pregnancy in the rat. J. Cell Biol. 110, 269–82.CrossRefGoogle ScholarPubMed
Snider, W.D.. (1994).Functions of the neurotrophins during nervous system development: what the knockouts are teaching us.Cell. 77,627–38.CrossRefGoogle ScholarPubMed
Stephens, R.M., Loeb, D.M., Copeland, T.D., Pawson, T.. Greene, L.A.. Kaplan, D.R.. (1994). Trk receptors use redundant signal transduction pathways involving SHC and PLC-gamma I to mediate NGF responses. Neuron. 12, 691705.CrossRefGoogle ScholarPubMed
Szeberényi, J., Erhardt, P.. (1994). Cellular components of nerve growth factor signaling. Biochim.Biophys. Acts. 1222, 187202.Google Scholar
Thoenen, H.. (1991). The changing scene of neurotrophic factors. Trends Neurosci. 14, 165–.CrossRefGoogle ScholarPubMed
Vetter, M.L.. Martin-Zanca, D.. Parada, L.F.. Bishop, J.M.. Kaplan, D.R.. (1991). Nerve growth factor rapidly stimulates tyrosine phosphorylation of phospholipase C-gamma 1 by a kinase activity associated with the product of the trk protooncogene. Proc. Natl. Acad. Sci. USA. 88, 5650–4.CrossRefGoogle ScholarPubMed
Wiesen, J.F.. Midgley, A.R. Jr. (1993). Changes in expression of connexin 43 gap junction messenger ribonucleic acid and protein during ovarian follicular growth. Endocrinology. 133, 741–6.CrossRefGoogle ScholarPubMed