Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures
Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. West...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Ando, H. [verfasserIn] Imamura, Y. [verfasserIn] Tadokoro, O. [verfasserIn] Hossin, M. Z. [verfasserIn] Unno, S. [verfasserIn] Sogawa, N. [verfasserIn] Kondo, E. [verfasserIn] Kitagawa, J. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2017 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Neurophysiology - New York, NY [u.a.] : Consultants Bureau, 1969, 49(2017), 4 vom: Aug., Seite 254-260 |
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| Übergeordnetes Werk: |
volume:49 ; year:2017 ; number:4 ; month:08 ; pages:254-260 |
| Links: |
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| DOI / URN: |
10.1007/s11062-017-9679-x |
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| Katalog-ID: |
SPR016217314 |
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| 100 | 1 | |a Ando, H. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures |
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| 520 | |a Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. Our observations suggest that CB-ir and CR-ir cells in the frog TD correspond to type-II and type-III cells, respectively. | ||
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| 650 | 4 | |a calbindin D28k |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a calretinin |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a taste cells |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a frog |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Imamura, Y. |e verfasserin |4 aut | |
| 700 | 1 | |a Tadokoro, O. |e verfasserin |4 aut | |
| 700 | 1 | |a Hossin, M. Z. |e verfasserin |4 aut | |
| 700 | 1 | |a Unno, S. |e verfasserin |4 aut | |
| 700 | 1 | |a Sogawa, N. |e verfasserin |4 aut | |
| 700 | 1 | |a Kondo, E. |e verfasserin |4 aut | |
| 700 | 1 | |a Kitagawa, J. |e verfasserin |4 aut | |
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10.1007/s11062-017-9679-x doi (DE-627)SPR016217314 (SPR)s11062-017-9679-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Ando, H. verfasserin aut Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. Our observations suggest that CB-ir and CR-ir cells in the frog TD correspond to type-II and type-III cells, respectively. calcium binding proteins (dpeaa)DE-He213 calbindin D28k (dpeaa)DE-He213 calretinin (dpeaa)DE-He213 taste cells (dpeaa)DE-He213 frog (dpeaa)DE-He213 Imamura, Y. verfasserin aut Tadokoro, O. verfasserin aut Hossin, M. Z. verfasserin aut Unno, S. verfasserin aut Sogawa, N. verfasserin aut Kondo, E. verfasserin aut Kitagawa, J. verfasserin aut Enthalten in Neurophysiology New York, NY [u.a.] : Consultants Bureau, 1969 49(2017), 4 vom: Aug., Seite 254-260 (DE-627)325573433 (DE-600)2037679-0 1573-9007 nnns volume:49 year:2017 number:4 month:08 pages:254-260 https://dx.doi.org/10.1007/s11062-017-9679-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 49 2017 4 08 254-260 |
| spelling |
10.1007/s11062-017-9679-x doi (DE-627)SPR016217314 (SPR)s11062-017-9679-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Ando, H. verfasserin aut Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. Our observations suggest that CB-ir and CR-ir cells in the frog TD correspond to type-II and type-III cells, respectively. calcium binding proteins (dpeaa)DE-He213 calbindin D28k (dpeaa)DE-He213 calretinin (dpeaa)DE-He213 taste cells (dpeaa)DE-He213 frog (dpeaa)DE-He213 Imamura, Y. verfasserin aut Tadokoro, O. verfasserin aut Hossin, M. Z. verfasserin aut Unno, S. verfasserin aut Sogawa, N. verfasserin aut Kondo, E. verfasserin aut Kitagawa, J. verfasserin aut Enthalten in Neurophysiology New York, NY [u.a.] : Consultants Bureau, 1969 49(2017), 4 vom: Aug., Seite 254-260 (DE-627)325573433 (DE-600)2037679-0 1573-9007 nnns volume:49 year:2017 number:4 month:08 pages:254-260 https://dx.doi.org/10.1007/s11062-017-9679-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 49 2017 4 08 254-260 |
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10.1007/s11062-017-9679-x doi (DE-627)SPR016217314 (SPR)s11062-017-9679-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Ando, H. verfasserin aut Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. Our observations suggest that CB-ir and CR-ir cells in the frog TD correspond to type-II and type-III cells, respectively. calcium binding proteins (dpeaa)DE-He213 calbindin D28k (dpeaa)DE-He213 calretinin (dpeaa)DE-He213 taste cells (dpeaa)DE-He213 frog (dpeaa)DE-He213 Imamura, Y. verfasserin aut Tadokoro, O. verfasserin aut Hossin, M. Z. verfasserin aut Unno, S. verfasserin aut Sogawa, N. verfasserin aut Kondo, E. verfasserin aut Kitagawa, J. verfasserin aut Enthalten in Neurophysiology New York, NY [u.a.] : Consultants Bureau, 1969 49(2017), 4 vom: Aug., Seite 254-260 (DE-627)325573433 (DE-600)2037679-0 1573-9007 nnns volume:49 year:2017 number:4 month:08 pages:254-260 https://dx.doi.org/10.1007/s11062-017-9679-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 49 2017 4 08 254-260 |
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10.1007/s11062-017-9679-x doi (DE-627)SPR016217314 (SPR)s11062-017-9679-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Ando, H. verfasserin aut Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. Our observations suggest that CB-ir and CR-ir cells in the frog TD correspond to type-II and type-III cells, respectively. calcium binding proteins (dpeaa)DE-He213 calbindin D28k (dpeaa)DE-He213 calretinin (dpeaa)DE-He213 taste cells (dpeaa)DE-He213 frog (dpeaa)DE-He213 Imamura, Y. verfasserin aut Tadokoro, O. verfasserin aut Hossin, M. Z. verfasserin aut Unno, S. verfasserin aut Sogawa, N. verfasserin aut Kondo, E. verfasserin aut Kitagawa, J. verfasserin aut Enthalten in Neurophysiology New York, NY [u.a.] : Consultants Bureau, 1969 49(2017), 4 vom: Aug., Seite 254-260 (DE-627)325573433 (DE-600)2037679-0 1573-9007 nnns volume:49 year:2017 number:4 month:08 pages:254-260 https://dx.doi.org/10.1007/s11062-017-9679-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 49 2017 4 08 254-260 |
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10.1007/s11062-017-9679-x doi (DE-627)SPR016217314 (SPR)s11062-017-9679-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Ando, H. verfasserin aut Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. Our observations suggest that CB-ir and CR-ir cells in the frog TD correspond to type-II and type-III cells, respectively. calcium binding proteins (dpeaa)DE-He213 calbindin D28k (dpeaa)DE-He213 calretinin (dpeaa)DE-He213 taste cells (dpeaa)DE-He213 frog (dpeaa)DE-He213 Imamura, Y. verfasserin aut Tadokoro, O. verfasserin aut Hossin, M. Z. verfasserin aut Unno, S. verfasserin aut Sogawa, N. verfasserin aut Kondo, E. verfasserin aut Kitagawa, J. verfasserin aut Enthalten in Neurophysiology New York, NY [u.a.] : Consultants Bureau, 1969 49(2017), 4 vom: Aug., Seite 254-260 (DE-627)325573433 (DE-600)2037679-0 1573-9007 nnns volume:49 year:2017 number:4 month:08 pages:254-260 https://dx.doi.org/10.1007/s11062-017-9679-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 49 2017 4 08 254-260 |
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English |
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Enthalten in Neurophysiology 49(2017), 4 vom: Aug., Seite 254-260 volume:49 year:2017 number:4 month:08 pages:254-260 |
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Enthalten in Neurophysiology 49(2017), 4 vom: Aug., Seite 254-260 volume:49 year:2017 number:4 month:08 pages:254-260 |
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calcium binding proteins calbindin D28k calretinin taste cells frog |
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Neurophysiology |
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Ando, H. @@aut@@ Imamura, Y. @@aut@@ Tadokoro, O. @@aut@@ Hossin, M. Z. @@aut@@ Unno, S. @@aut@@ Sogawa, N. @@aut@@ Kondo, E. @@aut@@ Kitagawa, J. @@aut@@ |
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2017-08-01T00:00:00Z |
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Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. 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Ando, H. |
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Ando, H. ddc 610 bkl 44.90 misc calcium binding proteins misc calbindin D28k misc calretinin misc taste cells misc frog Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures |
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610 ASE 44.90 bkl Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures calcium binding proteins (dpeaa)DE-He213 calbindin D28k (dpeaa)DE-He213 calretinin (dpeaa)DE-He213 taste cells (dpeaa)DE-He213 frog (dpeaa)DE-He213 |
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Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures |
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expression of calcium-binding proteins, calbindin d28k and calretinin, in the frog taste receptor structures |
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Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures |
| abstract |
Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. Our observations suggest that CB-ir and CR-ir cells in the frog TD correspond to type-II and type-III cells, respectively. |
| abstractGer |
Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. Our observations suggest that CB-ir and CR-ir cells in the frog TD correspond to type-II and type-III cells, respectively. |
| abstract_unstemmed |
Considering that information on the expression of calcium-binding proteins (CaBPs) in different cells of the taste receptors is rather limited, we investigated the distribution of such proteins, calbindin D28k (CB) and calretinin (CR), in the taste disc (TD) of the frog Lithobates catesbeianus. Western blot analysis revealed that CB and CR are expressed in cells of the fungiform papillae. CB-immunoreactive (ir) and CR-ir cell somata were located in the middle layer of the TD. Most CB-ir and CR-ir cells possessed one rod-shaped apical process and one basal process; in some cells there were several extended basal processes. Apical processes of CR-ir cells were thinner than those of CB-ir units, and CR-ir nerve fibers were ramified in the lamina propria directly below the TD. Most CR-ir fiber branches surrounded the TD; however, some penetrated this region, with both types of branches approaching the surface. CB and CR immunoreactivities did not co-occur in TD cells. In the TDs examined, the number of CB-ir cells was significantly greater than that of CR-ir units. Our observations suggest that CB-ir and CR-ir cells in the frog TD correspond to type-II and type-III cells, respectively. |
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4 |
| title_short |
Expression of Calcium-Binding Proteins, Calbindin D28k and Calretinin, in the Frog Taste Receptor Structures |
| url |
https://dx.doi.org/10.1007/s11062-017-9679-x |
| remote_bool |
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| author2 |
Imamura, Y. Tadokoro, O. Hossin, M. Z. Unno, S. Sogawa, N. Kondo, E. Kitagawa, J. |
| author2Str |
Imamura, Y. Tadokoro, O. Hossin, M. Z. Unno, S. Sogawa, N. Kondo, E. Kitagawa, J. |
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| doi_str |
10.1007/s11062-017-9679-x |
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2024-07-03T21:38:01.130Z |
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| score |
7.40086 |