Neogenesis of cerebellar Purkinje neurons from gene-marked bone marrow cells in vivo

J Priller, D A Persons, F F Klett, G Kempermann, G W Kreutzberg, U Dirnagl

Research output: Contribution to journalArticlepeer-review


The versatility of stem cells has only recently been fully recognized. There is evidence that upon adoptive bone marrow (BM) transplantation (BMT), donor-derived cells can give rise to neuronal phenotypes in the brains of recipient mice. Yet only few cells with the characteristic shape of neurons were detected 1-6 mo post-BMT using transgenic or newborn mutant mice. To evaluate the potential of BM to generate mature neurons in adult C57BL/6 mice, we transferred the enhanced green fluorescent protein (GFP) gene into BM cells using a murine stem cell virus-based retroviral vector. Stable and high level long-term GFP expression was observed in mice transplanted with the transduced BM. Engraftment of GFP-expressing cells in the brain was monitored by intravital microscopy. In a long-term follow up of 15 mo post-BMT, fully developed Purkinje neurons were found to express GFP in both cerebellar hemispheres and in all chimeric mice. GFP-positive Purkinje cells were also detected in BM chimeras from transgenic mice that ubiquitously express GFP. Based on morphologic criteria and the expression of glutamic acid decarboxylase, the newly generated Purkinje cells were functional.

Original languageEnglish
Pages (from-to)733-8
Number of pages6
JournalJournal of Cell Biology
Issue number5
Publication statusPublished - 26 Nov 2001


  • Animals
  • Bone Marrow Cells
  • Bone Marrow Transplantation
  • Cell Transplantation
  • Cerebellum
  • Flow Cytometry
  • Green Fluorescent Proteins
  • Hematopoietic Stem Cell Transplantation
  • Luminescent Proteins
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Confocal
  • Microscopy, Immunoelectron
  • Purkinje Cells
  • Recombinant Fusion Proteins
  • Retroviridae
  • Stem Cell Transplantation
  • Stem Cells
  • Transduction, Genetic
  • Transplantation Chimera
  • Transplantation, Isogeneic
  • Journal Article
  • Research Support, Non-U.S. Gov't


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