Pre-Bötzinger complex neurokinin-1 receptor expressing neurons in primary cell culture
Phenotypic identification of pre-Bötzinger complex (pre-BötC) neurons is vital to the delineation of endogenous cellular properties involved in respiratory rhythm generation and neuromodulation of breathing. A subpopulation of pre-BötC neurons endowed with intrinsic rhythmicity is proposed as the ke...
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Published in | Advances in experimental medicine and biology Vol. 605; p. 94 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
United States
2008
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Abstract | Phenotypic identification of pre-Bötzinger complex (pre-BötC) neurons is vital to the delineation of endogenous cellular properties involved in respiratory rhythm generation and neuromodulation of breathing. A subpopulation of pre-BötC neurons endowed with intrinsic rhythmicity is proposed as the kernel for inspiratory rhythm generation in vitro. In this study, the pre-BötC "island" preparation was excised from medullary slices and reduced to its heterogeneous cellular constituents using primary cell culture techniques. Cultured neurons were labeled with tetramethylrhodamine conjugated to Substance P (TMR-SP) to identify individual NK-1R expressing neurons. Data from this study provide initial evidence that the pre-BötC neurons living in culture remain functionally capable of binding and internalizing the fluorescently-tagged ligand and TMR-SP tagging is a useful experimental tool that reliably identifies the NK-1R phenotype. |
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AbstractList | Phenotypic identification of pre-Bötzinger complex (pre-BötC) neurons is vital to the delineation of endogenous cellular properties involved in respiratory rhythm generation and neuromodulation of breathing. A subpopulation of pre-BötC neurons endowed with intrinsic rhythmicity is proposed as the kernel for inspiratory rhythm generation in vitro. In this study, the pre-BötC "island" preparation was excised from medullary slices and reduced to its heterogeneous cellular constituents using primary cell culture techniques. Cultured neurons were labeled with tetramethylrhodamine conjugated to Substance P (TMR-SP) to identify individual NK-1R expressing neurons. Data from this study provide initial evidence that the pre-BötC neurons living in culture remain functionally capable of binding and internalizing the fluorescently-tagged ligand and TMR-SP tagging is a useful experimental tool that reliably identifies the NK-1R phenotype. |
Author | Johnson, Shereé M |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18085253$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Animals Biological Clocks - physiology Cell Culture Techniques Nerve Net - physiology Neurons - cytology Neurons - physiology Receptors, Neurokinin-1 - physiology Respiratory Physiological Phenomena |
Title | Pre-Bötzinger complex neurokinin-1 receptor expressing neurons in primary cell culture |
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