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. 2006 Apr 5;8(2):253–261. doi: 10.1111/j.1750-3639.1998.tb00151.x

BDNF Up‐Regulates TrkB Protein and Prevents the Death of CA1 Neurons Following Transient Forebrain Ischemia

Isidre Ferrer 1,2,, Jordi Ballabriga 1, Eulalia Martí 2, Esther Pérez 2, Jordi Alberch 2, Ernest Arenas 3
PMCID: PMC8098442  PMID: 9546284

Abstract

The neurotrophin family of growth factors, which includes Nerve Growth Factor (NGF), Brain‐Derived Neurotrophic Factor (BDNF), Neurotrophin‐3 (NT3) and Neurotrophin‐4/5 (NT4/5) bind and activate specific tyrosine kinase (Trk) receptors to promote cell survival and growth of different cell populations. For these reasons, growing attention has been paid to the use of neurotrophins as therapeutic agents in neurodegeneration, and to the regulation of the expression of their specific receptors by the ligands. BDNF expression, as revealed by immunohistochemistry, is found in the pre‐subiculum, CA1, CA3, and dentate gyrus of the hippocampus. Strong TrkB immunoreactivity is present in most CA3 neurons but only in scattered neurons of the CA1 area. Weak TrkB immunoreactivity is found in the granule cell layer of the dentate gyrus. Unilateral grafting of BDNF‐transfected fibroblasts into the hippocampus resulted in a marked increase in the intensity of the immunoreaction and in the number of TrkB‐immunoreactive neurons in the granule cell layer of the dentate gyrus, pre‐subiculum and CA1 area in the vicinity of the graft. No similar effects were produced after the injection of control mock‐transfected fibroblasts. Delayed cell death in the CA1 area was produced following 5 min of forebrain ischemia in the gerbil. The majority of living cells in the CA1 area at the fourth day were BDNF/TrkB immunoreactive. Unilateral grafting of control mock‐transfected or BDNF fibroblasts two days before ischemia resulted in a moderate non‐specific protection of TrkB‐negative, but not TrkB‐positive cells, in the CA1 area of the grafted side. This finding is in line with a vascular and glial reaction, as revealed, by immunohistochemistry using astroglial and microglial cell markers. This astroglial response was higher in the grafted side than in the contralateral side in ischemic gerbils, but no differences were seen between BDNF‐producing and non‐BDNF‐producing grafts. However, grafting of BDNF‐producing fibroblasts two days before ischemia significantly and specifically prevented nerve cells from dying in the CA1 area of the ipsilateral hippocampus. Cell survival was associated with increased TrkB immunoreactivity as the majority of living cells were TrkB immunoreactive. Thus, our results show that BDNF is able to up‐regulate the expression of TrkB in control and pathological states, and that BDNF prevention of neuronal death following transient forebrain ischemia is associated with increased expression of its specific receptor.

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References

  • 1. Acarín L, Vela JM, González B, Castellano B (1994) Demonstration of poly‐N‐acetyl lactosamine residues in ameboid and ramified microglial cells in rat brain by tomato lectin binding. J Histochem Cytochem 42: 1033–1041. [DOI] [PubMed] [Google Scholar]
  • 2. Acheson A, Conover JC, Fandl JP, DeChiara TM, Russell M, Thadani M, Squinto SP, Yancopoulos GD, Lindsay RM (1995) A BDNF autocrine loop in adult sensory neurons prevents cell death. Nature 374: 450–453. [DOI] [PubMed] [Google Scholar]
  • 3. Arenas E, Persson H (1994) Neurotrophin‐3 prevents the death of adult noradrenergic neurons in vivo. Nature 367:368–371. [DOI] [PubMed] [Google Scholar]
  • 4. Barbacid M (1995) Structural and functional properties of the Trk family of neurotrophin receptors. Ann NY Acad Sci 766: 442–458. [DOI] [PubMed] [Google Scholar]
  • 5. Barde YA (1994) Neurotrophins: a family of proteins supporting the survival of neurons. Prog Clin Biol Res 390: 45–56. [PubMed] [Google Scholar]
  • 6. Beck T, Lindholm D, Castren E, Wree A (1994) Brain‐derived neurotrophic factor protects against ischemiccell damage in rat hippocampus. J Cereb Blood Flow Metab 14: 689–692. [DOI] [PubMed] [Google Scholar]
  • 7. Bothwell M (1995) Functional interactions of neurotrophins and neurotrophin receptors. Annu Rev Neurosci 18: 223–253. [DOI] [PubMed] [Google Scholar]
  • 8. Carter BD, Zirrgiebeld U, Barde YA (1995) Differentialregulation of p21 ras activation in neurons by nervegrowth factor and brain‐derived growth factor. J Biol Chem 270: 21751–21757. [DOI] [PubMed] [Google Scholar]
  • 9. Dugich‐Djordjevic MM, Peterson C, Isono F, Ohsawa F, Widmer HR, Denton TL, Bennett GL, Hefti F (1995) Immunohistochemical visualization of brain‐derived neurotrophic factor in the rat brain. Eur J Neurosci 7: 1831–1839. [DOI] [PubMed] [Google Scholar]
  • 10. Ferrer I, Ballabriga J, Marti E, Pozas E, Planas AM, Blasi J (1997) BDNF and TrkB co‐localize in CA1 neurons resistant to transient forebrain ischemia in the adult gerbil. J Neuropathol Exp Neurol 56: 790–797. [PubMed] [Google Scholar]
  • 11. Ferrer I, Tortosa A, Macaya A, Sierra A, Moreno D, Munell F, Blanco R, Squier W (1994) Evidence of nuclear DNA fragmentation following hypoxia‐ischemia in the infant rat brain, and transient forebrain ischemia in the adult gerbil. Brain Pathol 4: 115–122. [DOI] [PubMed] [Google Scholar]
  • 12. Frank L, Ventimiglia R, Anderson K, Lindsay RM, Rudge JS (1996) BDNF down‐regulates neurotrophin responsiveness, TrkB protein and trkB mRNA levels in cultured rat hippocampal neurons. Eur J Neurosci 8: 1220–1230. [DOI] [PubMed] [Google Scholar]
  • 13. Gosh A, Carnahan J, Greenberg ME (1994) Requirements for BDNF in activity‐dependent survival of cortical neurons. Science 263: 1618–1623. [DOI] [PubMed] [Google Scholar]
  • 14. Hara H, Sakamoto T, Kogure K (1993) Mechanisms and pathogenesis of ischaemia‐induced neuronal damage. Progr Neurobiol 40: 645–670. [DOI] [PubMed] [Google Scholar]
  • 15. Hofer M, Barde YA (1992) Brain‐derived neurotropfactor prevents neuronal death in vivo. Nature 331: 261–262. [DOI] [PubMed] [Google Scholar]
  • 16. Holtzman DM, Li Y, Parada LF, Kinsman S, Chen CK, Valletta JS, Zhou J, Long JB, Mobley WC (1992) p140trk mRNA marks NGF‐responsive forebrain neurons: evidence that trk gene expression is induced by NGF. Neuron 9:465–478. [DOI] [PubMed] [Google Scholar]
  • 17. Ibañez CF (1994) Structure‐function relationships inneurotrophin family. J Neurobiol 25: 1349–1361. [DOI] [PubMed] [Google Scholar]
  • 18. Ito U, Spatz M, Walker JT, Klatzo I (1975) Experimentalcerebral ischemia in Mongolian gerbils. I. Light micro‐scopical observations. Acta Neuropathol 32: 209–223. [DOI] [PubMed] [Google Scholar]
  • 19. Ito U, Yamaguchi T, Tomita H, Tone O, Shishido T, Hayashi H, Yoshida M (1992) Maturation of ischemic injuries observed in Mongolian gerbils: Introductory remarks. In: Maturation phenomenon in cerebral ischemia, Ito U, Kirino T, Kuroiwa T, Klatzo I, (Eds.), pp. 1–13, Springer‐Verlag: Berlin , Heidelberg , New York . [Google Scholar]
  • 20. Kirino T (1992) Delayed neuronal death in the gerbilhippocampus following ischemia. Brain Res 239: 57–69. [DOI] [PubMed] [Google Scholar]
  • 21. Knusel B, Beck KD, Winslow JW, Rosenthal A, Burton LE, Widmer HR, Nikolics K, Hefti F (1992) Brain‐derived neurotrophic factor administration protects basal forebrain cholinergic but not nigral dopaminergic neurons from degenerative changes after axotomy in the adult rat brain. J Neurosci 12: 4391–4402. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Knusel B, Gao H, Okazaki T, Yoshida T, Mori N, Hefti F, Kaplan DR (1997) Ligand‐induced down‐regulation of trk messenger RNA, protein and tyrosine phosphorylation in rat cortical neurons. Neuroscience 78: 851–862. [DOI] [PubMed] [Google Scholar]
  • 23. Knusel B, Kaplan D, Hefti F (1996) Intraparenchymal NGF injections in adult and aged rats induce long‐lasting Trk tyrosyne phosphorylation. Exp Neurol 139: 121–130. [DOI] [PubMed] [Google Scholar]
  • 24. Knusel B, Rabin SJ, Hefti F, Kaplan DR (1994) Regulated neurotrophin receptor responsiveness during neuronal migration and early differentiation. J Neurosci 14: 1542–1554. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Knusel B, Rabin S, Widmer HR, Hefti F, Kaplan DR (1992) Neurotrophin‐induced trk receptor phosphorylation and cholinergic neuron response in primary cultures of embryonic rat brain neurons. NeuroReport 3: 885–888. [DOI] [PubMed] [Google Scholar]
  • 26. Kokaia Z, Bengzon J, Metsis M, Kokaia M, Persson H, Lindvall O (1993) Coexpression of neurotrophins and their receptors in neurons of the central nervous system. Proc Natl Acad Sci USA 90: 6711–6715. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Koliatsos VE, Clatterbuck RE, Winslow JW, Cayouette MH, Price DL (1993) Evidence that brain‐derived neurotrophic factor is a trophic factor for motor neurons in vivo. Neuron 10: 359–367. [DOI] [PubMed] [Google Scholar]
  • 28. Lewin GR, Barde YA (1996) Physiology of the neurotrophins. Annu Rev Neurosci 19: 289–317. [DOI] [PubMed] [Google Scholar]
  • 29. Martínez‐Serrano A, Hantzopoulos PA, Björklund A (1996) Ex vivo gene transfer of brain‐derived neurotrophic factor to the intact rat forebrain: neurotrophic effects on cholinergic neurons. Eur J Neurosci 8: 727–735. [DOI] [PubMed] [Google Scholar]
  • 30. Morse JK, Wiegand SJ, Anderson K, You Y, Cai N, Carnahan J, Miller J, DiStefano PS, Altar CA, Lindsay RM, Alderson RF (1993) Brain‐derived neurotrophic factor (BDNF) prevents the degeneration of medial septal cholinergic neurons following fimbria transection. J Neurosci 13: 4146–4156. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Mu X, Silos‐Santiago I, Carroll SL, Snider WD (1993) Neurotrophin receptor genes are expressed in distinct patterns in developing dorsal root ganglia. J Neurosci 13: 4029–4041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Neveu I, Arenas E (1996) Neurotrophins promote the survival and development of neurons in the cerebellum of hypothyroid rats in vivo. J Cell Biol 133: 631–646. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Nieto‐Sampedro M, Lewis ER, Cotman CW, Manthpe M, Skaper SD, Barbin G, Longo FM, Varon S (1982) Brain injury causes a time‐dependent increase in neurotrophic activity at the lesion site. Science 217: 860–861. [DOI] [PubMed] [Google Scholar]
  • 34. Schmidt‐Kastner R, Wetmore C, Olson L (1996) Comparative study of brain derived neurotrophic factor messenger RNA and protein at the cellular level suggests multiple roles in hippocampus, striatum and cortex. Neuroscience 74: 161–183. [DOI] [PubMed] [Google Scholar]
  • 35. Tortosa A, Ferrer I (1993) Parvalbumin immunoreactivity in the hippocampus of the gerbil after transient forebrain ischaemia: a qualitative and quantitative sequential study. Neuroscience 55: 33–43. [DOI] [PubMed] [Google Scholar]
  • 36. Tsukahara T, Yonekawa Y, Tanaka F, Ohara O, Wantanabe S, Kimura T, Nishijima T, Taniguchi T (1994) The role of brain‐derived neurotrophic factor in transient forebrain ischemia in the rat brain. Neurosurgery 34: 323–331. [DOI] [PubMed] [Google Scholar]
  • 37. Widmer HR, Knusel B, Hefti F (1993) BDNF protection of basal forebrain cholinergic neurons after axotomy: complete protection of p75NGFR‐positive cells. Neuro- Report 4: 363–366. [DOI] [PubMed] [Google Scholar]
  • 38. Wright DE, Snider WD (1995) Neurotrophin receptor mRNA expression defines distinct populations of neurons in rat dorsal root ganglia. J Comp Neurol 351: 329–338. [DOI] [PubMed] [Google Scholar]
  • 39. Yan Q, Elliott J, Snider WD (1992) Brain‐derived neurotrophic factor rescues spinal motor neurons from axotomy‐induced cell death. Nature 360: 753–755. [DOI] [PubMed] [Google Scholar]
  • 40. Zhou XF, Parada LF, Soppet D, Rush RA (1993) Distribution of trkB tyrosyne kinase immunoreactivity in the rat central nervous system. Brain Res 17: 63–70. [DOI] [PubMed] [Google Scholar]

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