Coexpression of neurocalcin with other calcium-binding proteins in the rat main olfactory bulb
The distribution patterns of four calcium‐binding proteins (CaBPs)—calbindin D‐28k (CB), calretinin (CR), neurocalcin (NC), and parvalbumin (PV)—in the rat main olfactory bulb were compared, and the degrees of colocalization of NC with the other CaBPs were determined by using double immunocytochemic...
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Published in: | Journal of comparative neurology (1911) Vol. 407; no. 3; pp. 404 - 414 |
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Abstract | The distribution patterns of four calcium‐binding proteins (CaBPs)—calbindin D‐28k (CB), calretinin (CR), neurocalcin (NC), and parvalbumin (PV)—in the rat main olfactory bulb were compared, and the degrees of colocalization of NC with the other CaBPs were determined by using double immunocytochemical techniques.
All investigated CaBPs were detected in groups of periglomerular cells and Van Gehuchten cells, whereas other cell types expressed some of the investigated proteins but not all four. Double‐labeling techniques demonstrated the colocalization of NC with CB, CR, or PV in periglomerular cells, whereas each neurochemical group constituted entirely segregated populations in the remaining neuronal types. This is evident in granule cells that demonstrated large but segregated populations immunoreactive to either NC or CR.
This study provides a further biochemical characterization of interneuronal types in the rat main olfactory bulb. On the basis of the distinct calcium‐binding affinities, each neurochemically defined population may have different responses to calcium influx that would result in the existence of distinct functional subgroups within morphologically defined neuronal types. The expression of the investigated CaBPs in periglomerular cells with both single and colocalized patterns suggests that the local circuits in the glomerular layer are constituted by a complex network of elements with particular calcium requirements. J. Comp. Neurol. 407:404–414, 1999. © 1999 Wiley‐Liss, Inc. |
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AbstractList | The distribution patterns of four calcium-binding proteins (CaBPs) - calbindin D-28k (CB), calretinin (CR), neurocalcin (NC), and parvalbumin (PV) - in the rat main olfactory bulb were compared, and the degrees of colocalization of NC with the other CaBPs were determined by using double immunocytochemical techniques. All investigated CaBPs were detected in groups of periglomerular cells and Van Gehuchten cells, whereas other cell types expressed some of the investigated proteins but not all four. Double-labeling techniques demonstrated the colocalization of NC with CB, CR, or PV in periglomerular cells, whereas each neurochemical group constituted entirely segregated populations in the remaining neuronal types. This is evident in granule cells that demonstrated large but segregated populations immunoreactive to either NC or CR. This study provides a further biochemical characterization of interneuronal types in the rat main olfactory bulb. On the basis of the distinct calcium-binding affinities, each neurochemically defined population may have different responses to calcium influx that would result in the existence of distinct functional subgroups within morphologically defined neuronal types. The expression of the investigated CaBPs in periglomerular cells with both single and colocalized patterns suggests that the local circuits in the glomerular layer are constituted by a complex network of elements with particular calcium requirements. The distribution patterns of four calcium-binding proteins (CaBPs)-calbindin D-28k (CB), calretinin (CR), neurocalcin (NC), and parvalbumin (PV)-in the rat main olfactory bulb were compared, and the degrees ofcolocalization of NC with the other CaBPs were determined by using double immunocytochemical techniques. All investigated CaBPs were detected in groups of periglomerular cells and Van Gehuchten cells, whereas other cell types expressed some of the investigated proteins but not all four. Double-labeling techniques demonstrated the colocalization of NC with CB, CR, or PV in periglomerular cells, whereas each neurochemical group constituted entirely segregated populations in the remaining neuronal types. This is evident in granule cells that demonstrated large but segregated populations immunoreactive to either NC or CR. This study provides a further biochemical characterization of interneuronal types in the rat main olfactory bulb. On the basis of the distinct calcium-binding affinities, each neurochemically defined population may have different responses to calcium influx that would result in the existence of distinct functional subgroups within morphologically defined neuronal types. The expression of the investigated CaBPs in periglomerular cells with both single and colocalized patterns suggests that the local circuits in the glomerular layer are constituted by a complex network of elements with particular calcium requirements. The distribution patterns of four calcium‐binding proteins (CaBPs)—calbindin D‐28k (CB), calretinin (CR), neurocalcin (NC), and parvalbumin (PV)—in the rat main olfactory bulb were compared, and the degrees of colocalization of NC with the other CaBPs were determined by using double immunocytochemical techniques. All investigated CaBPs were detected in groups of periglomerular cells and Van Gehuchten cells, whereas other cell types expressed some of the investigated proteins but not all four. Double‐labeling techniques demonstrated the colocalization of NC with CB, CR, or PV in periglomerular cells, whereas each neurochemical group constituted entirely segregated populations in the remaining neuronal types. This is evident in granule cells that demonstrated large but segregated populations immunoreactive to either NC or CR. This study provides a further biochemical characterization of interneuronal types in the rat main olfactory bulb. On the basis of the distinct calcium‐binding affinities, each neurochemically defined population may have different responses to calcium influx that would result in the existence of distinct functional subgroups within morphologically defined neuronal types. The expression of the investigated CaBPs in periglomerular cells with both single and colocalized patterns suggests that the local circuits in the glomerular layer are constituted by a complex network of elements with particular calcium requirements. J. Comp. Neurol. 407:404–414, 1999. © 1999 Wiley‐Liss, Inc. |
Author | Alonso, J.R. Okazaki, K. Hidaka, H. Arévalo, R. Briñón, J.G. Aijón, J. Bravo, I.G. Martínez-Guijarro, F.J. Crespo, C. |
Author_xml | – sequence: 1 givenname: J.G. surname: Briñón fullname: Briñón, J.G. organization: Departamento de Biología Celular y Patología, Universidad de Salamanca, E-37007 Salamanca, Spain – sequence: 2 givenname: F.J. surname: Martínez-Guijarro fullname: Martínez-Guijarro, F.J. organization: Unidad de Biología Celular, Facultad de Biología, Universidad de Valencia, E-46100 Burjasot, Spain – sequence: 3 givenname: I.G. surname: Bravo fullname: Bravo, I.G. organization: Departamento de Biología Celular y Patología, Universidad de Salamanca, E-37007 Salamanca, Spain – sequence: 4 givenname: R. surname: Arévalo fullname: Arévalo, R. organization: Departamento de Biología Celular y Patología, Universidad de Salamanca, E-37007 Salamanca, Spain – sequence: 5 givenname: C. surname: Crespo fullname: Crespo, C. organization: Departamento de Biología Celular y Patología, Universidad de Salamanca, E-37007 Salamanca, Spain – sequence: 6 givenname: K. surname: Okazaki fullname: Okazaki, K. organization: Department of Pharmacology, Nagoya University School of Medicine, Nagoya 466, Japan – sequence: 7 givenname: H. surname: Hidaka fullname: Hidaka, H. organization: Department of Pharmacology, Nagoya University School of Medicine, Nagoya 466, Japan – sequence: 8 givenname: J. surname: Aijón fullname: Aijón, J. organization: Departamento de Biología Celular y Patología, Universidad de Salamanca, E-37007 Salamanca, Spain – sequence: 9 givenname: J.R. surname: Alonso fullname: Alonso, J.R. email: jralonso@gugu.usal.es organization: Departamento de Biología Celular y Patología, Universidad de Salamanca, E-37007 Salamanca, Spain |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/10320220$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/0006-8993(84)90512-2 10.1007/BF00239586 10.1083/jcb.105.3.1343 10.1016/0306-4522(89)90434-X 10.1016/0006-8993(95)00326-L 10.1038/294765a0 10.1016/S0006-291X(05)81534-7 10.1177/29.4.6166661 10.1016/0306-4522(92)90525-7 10.1016/0304-3940(85)90408-2 10.1016/S0968-0004(06)80021-6 10.1074/jbc.271.17.10256 10.1002/cne.903540308 10.1016/S0168-0102(98)00002-9 10.1016/0304-3940(93)90285-S 10.1016/0306-4522(92)90012-Q 10.1002/cne.902190308 10.1016/0301-0082(87)90024-4 10.1002/cne.902170209 10.1016/S0006-8993(98)00311-4 10.1007/BF00319620 10.1016/0143-4160(90)90014-L 10.1016/S0306-4522(96)00308-9 10.1002/cne.902350408 10.1016/0143-4160(88)90027-9 10.1016/0306-4522(90)90091-H |
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Snippet | The distribution patterns of four calcium‐binding proteins (CaBPs)—calbindin D‐28k (CB), calretinin (CR), neurocalcin (NC), and parvalbumin (PV)—in the rat... The distribution patterns of four calcium-binding proteins (CaBPs)-calbindin D-28k (CB), calretinin (CR), neurocalcin (NC), and parvalbumin (PV)-in the rat... The distribution patterns of four calcium-binding proteins (CaBPs) - calbindin D-28k (CB), calretinin (CR), neurocalcin (NC), and parvalbumin (PV) - in the rat... |
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SubjectTerms | Animals Calbindin 2 calbindin D-28k Calbindins Calcium-Binding Proteins - metabolism calretinin Immunohistochemistry Male Nerve Tissue Proteins - metabolism Neurocalcin Neurons - metabolism Olfactory Bulb - cytology Olfactory Bulb - metabolism olfactory system parvalbumin Parvalbumins - metabolism Rats - metabolism Rats, Wistar Receptors, Calcium-Sensing S100 Calcium Binding Protein G - metabolism specific cell markers Tissue Distribution - physiology |
Title | Coexpression of neurocalcin with other calcium-binding proteins in the rat main olfactory bulb |
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