Transforming growth factor-alpha (TGF alpha) enhances neuronal survival and neurite outgrowth in cull tured dorsal root ganglia (DRG) sensory neurons. It binds a membrane protein. denominated epidermal growth factor receptor (EGFr). EGFr has been localized in developing and adult human DRG. However, it remains to be elucidated whether all DRG neurons express EGFr or whether differences exist among neuronal subtypes. This study was undertaken to investigate these topics in adult human DRG using immunoblotting, and combined immunohistochemistry and image analysis techniques. A mouse monoclonal antibody (clone F4) mapping within the intracytoplasmic domain of EGFr was used. Immunoblotting revealed two main proteins with estimated molecular masses of approximate to 65 kDa and 170 kDa acid thus consistent with the full-length EGFr. Additional protein bands were also encountered. Light immunohistochemistry revealed specific immunoreactivity (IR) for EGFr-like proteins in most (86%) primary sensory neurons. the intensity of immunostaining being stronger in the small acid intermediate-sized ones. Furthermore. EGFr-like IR was also observed in the satellite glial cells of the ganglia as well as in the intraganglionic and dorsal root Schwann cells. Taken together. our findings demonstrate that EGFr, and other related proteins containing the epitope labeled with the antibody F4. are responsible for the EGFr IR reported in DRG. Furthermore, we demonstrated heterogeneity in the expression of EGFr-like IR in adult human primary sensory neurons. which suggests different responsiveness to their ligands.
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Univ Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, ItalyUniv Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, Italy
Biagioni, S
Tata, AM
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Univ Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, ItalyUniv Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, Italy
Tata, AM
Agrati, C
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Univ Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, ItalyUniv Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, Italy
Agrati, C
Cianfarani, F
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Univ Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, ItalyUniv Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, Italy
Cianfarani, F
Augusti-Tocco, G
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Univ Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, ItalyUniv Roma La Sapienza, Dipartimento Biol Cellulare & Sviluppo, I-00185 Rome, Italy
机构:St Bartholomews & Royal London Sch Med & Dent, Acad Dept Neurol, London E1 1BB, England
Bär, KJ
Saldanha, GJF
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机构:St Bartholomews & Royal London Sch Med & Dent, Acad Dept Neurol, London E1 1BB, England
Saldanha, GJF
Kennedy, AJ
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机构:St Bartholomews & Royal London Sch Med & Dent, Acad Dept Neurol, London E1 1BB, England
Kennedy, AJ
Facer, P
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机构:St Bartholomews & Royal London Sch Med & Dent, Acad Dept Neurol, London E1 1BB, England
Facer, P
Birch, R
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机构:St Bartholomews & Royal London Sch Med & Dent, Acad Dept Neurol, London E1 1BB, England
Birch, R
Carlstedt, T
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机构:St Bartholomews & Royal London Sch Med & Dent, Acad Dept Neurol, London E1 1BB, England
Carlstedt, T
Anand, P
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St Bartholomews & Royal London Sch Med & Dent, Acad Dept Neurol, London E1 1BB, EnglandSt Bartholomews & Royal London Sch Med & Dent, Acad Dept Neurol, London E1 1BB, England