Carbocyanine Postmortem Neuronal Tracing: Influence of Different Parameters on Tracing Distance and Combination with Immunocytochemistry

SUMMARY Carbocyanines (DiI, DiA, DiO) are able to travel along membranes by diffusion and therefore have been used as postmortem neuronal tracers in aldehyde-fixed tissues. Surprisingly, detailed data on the influence of different parameters on tracing distances are still missing. This study was carried out to optimize tracing procedures and to reveal the validity of the combination of postmortem tracing with immunocytochemistry. Carbocyanine crystals were applied to the cervical spinal cord, sciatic nerves, and brachial plexuses of humans and guinea pigs. Incubation in the dark at 37C for 12-15 weeks proved optimal to achieve longest tracing distances (28.9 ± 2.2 mm) in human and animal tissues. Longer incubation times and incubation temperatures higher than 37C did not result in longer tracing distances. No differences were evident between adult and newborn animals and between central and peripheral nervous system. The diffusion coefficient for DiI was calculated to be 2.5 × 10-7 cm2sec-1. After application of DiI to nerves of guinea pig extraocular muscles, DiI-positive afferent perikarya were observed in the anteromedial part of the trigeminal ganglion. These perikarya were identified by calcitonin gene-related peptide immunoreactivity (CGRP-IR). The percentage of CGRP-IR neurons after tracing was concordant with the percentage of CGRP-IR in trigeminal ganglia exclusively processed for CGRP-IR without previous postmortem tracing. These results demonstrate carbocyanines to be specific tracers for exact neuronal mapping studies.

[1]  W. Webb,et al.  Lateral transport of a lipid probe and labeled proteins on a cell membrane. , 1977, Science.

[2]  M. G. Honig,et al.  Fluorescent carbocyanine dyes allow living neurons of identified origin to be studied in long-term cultures , 1986, The Journal of cell biology.

[3]  S. Thanos,et al.  Major role for neuronal death during brain development: refinement of topographical connections. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[4]  S. Thanos,et al.  Axonal arborization in the developing chick retinotectal system , 1987, The Journal of comparative neurology.

[5]  S. Thanos,et al.  A study in developing visual systems with a new method of staining neurones and their processes in fixed tissue. , 1987, Development.

[6]  S. Thanos Morphology of ganglion cell dendrites in the albino rat retina: an analysis with fluorescent carbocyanine dyes. , 1988, Journal fur Hirnforschung.

[7]  A. Aguayo,et al.  Persistent retrograde labeling of adult rat retinal ganglion cells with the carbocyanine dye diI , 1988, Experimental Neurology.

[8]  A. Burkhalter,et al.  Organization of corticocortical connections in human visual cortex. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[9]  S. Easter,et al.  The development of the Xenopus retinofugal pathway: optic fibers join a pre-existing tract. , 1989, Development.

[10]  M. G. Honig,et al.  Dil and DiO: versatile fluorescent dyes for neuronal labelling and pathway tracing , 1989, Trends in Neurosciences.

[11]  S. Thanos,et al.  Spatial arrangement of radial glia and ingrowing retinal axons in the chick optic tectum during development. , 1989, Brain research. Developmental brain research.

[12]  S. Thanos,et al.  The developing chick isthmo-optic nucleus forms a transient efferent projection to the optic tectum , 1990, Neuroscience Letters.

[13]  E. W. Rubel,et al.  Neuronal tracing with DiI: decalcification, cryosectioning, and photoconversion for light and electron microscopic analysis. , 1990, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[14]  Bernd Fritzsch,et al.  Dextran amines in neuronal tracing , 1990, Trends in Neurosciences.

[15]  Jeffrey H. Kordower,et al.  Tracing neuronal connections in postmortem human hippocampal complex with the carbocyanine dye DiI , 1990, Neurobiology of Aging.

[16]  M. G. Honig,et al.  Double-labeling of tissue containing the carbocyanine dye DiI for immunocytochemistry. , 1990, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[17]  E. Stopa,et al.  Labeling of human retinohypothalamic tract with the carbocyanine dye, DiI , 1991, Brain Research.

[18]  R. Northcutt,et al.  The visually related posterior pretectal nucleus in the non‐percomorph teleost Osteoglossum bicirrhosum projects to the hypothalamus: A Dil study , 1991, The Journal of comparative neurology.

[19]  F. Valverde,et al.  A method using diI to study the connectivity of cortical transplants , 1991, Journal of Neuroscience Methods.

[20]  P. Ekström,et al.  Dil tracing in combination with immunocytochemistry for analysis of connectivities and chemoarchitectonics of specific neural systems in a teleost, the atlantic salmon , 1992, Journal of Neuroscience Methods.

[21]  C. Sotelo,et al.  Development of the olivocerebellar projection in the rat: I. Transient biochemical compartmentation of the inferior olive , 1992, The Journal of comparative neurology.

[22]  G. Papadopoulos,et al.  DiI labeling combined with conventional immunocytochemical techniques for correlated light and electron microscopic studies , 1993, Journal of Neuroscience Methods.

[23]  B. Schickinger [Central labeling of sacculo-cochlear neuronal connection]. , 1993, Wiener klinische Wochenschrift.

[24]  R. Anadón,et al.  Afferent and efferent connections of the habenula in the larval sea lamprey (Petromyzon marinus L.): An experimental study , 1994, The Journal of comparative neurology.

[25]  R. Magoul,et al.  Visualization of an efferent projection route of the hypothalamic rat arcuate nucleus through the stria terminalis after labeling with carbocyanine dye (DiI) or proopiomelanocortin-immunohistochemistry , 1994, Neuroscience Letters.

[26]  J. Morrison,et al.  Spindle neurons of the human anterior cingul. Ate cortex , 1995, The Journal of comparative neurology.

[27]  W. Snider,et al.  Development of the primary afferent projection in human spinal cord , 1995, The Journal of comparative neurology.

[28]  M. G. Honig,et al.  The expression of cell adhesion molecules on the growth cones of chick cutaneous and muscle sensory neurons. , 1995, Developmental biology.

[29]  R. Anadón,et al.  Neurons of the olfactory organ projecting to the caudal telencephalon and hypothalamus: a carbocyanine-dye labelling study in the brown trout (Teleostei) , 1995, Neuroscience Letters.

[30]  M. Byers,et al.  Odontoblast processes in dentin revealed by fluorescent Di-I. , 1995, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[31]  M. Heredia,et al.  Peripherin fibers in the main olfactory bulb are different from olfactory fibers and from LHRH fibers: an immunocytochemical and DiI study , 1996, Brain Research.

[32]  R. Coggeshall,et al.  Methods for determining numbers of cells and synapses: A case for more uniform standards of review , 1996, The Journal of comparative neurology.

[33]  Sensory innervation of the guinea pig extraocular muscles: A 1,1′‐dioctadecyl‐3,3,3′3′‐tetramethylindocarbocyanine perchlorate tracing and calcitonin gene‐related peptide immunohistochemical study , 1997, The Journal of comparative neurology.

[34]  M. Aigner,et al.  Somatotopic organization of primary afferent perikarya of the guinea-pig extraocular muscles in the trigeminal ganglion: a post-mortem DiI-tracing study. , 2000, Experimental eye research.