» Articles » PMID: 6194004

Diamidino Yellow Dihydrochloride (DY . 2HCl); a New Fluorescent Retrograde Neuronal Tracer, Which Migrates Only Very Slowly out of the Cell

Overview
Journal Exp Brain Res
Specialty Neurology
Date 1983 Jan 1
PMID 6194004
Citations 62
Authors
Affiliations
Soon will be listed here.
Abstract

Earlier studies showed that Nuclear Yellow (NY), True Blue (TB) and Fast Blue (FB) are transported retrogradely through axons to their parent cell bodies. NY produces a yellow fluorescent labeling of the neuronal nucleus at 360 nm excitation wavelength, while TB and FB produce a blue fluorescence of the cytoplasm at this same wavelength. Therefore, NY may be combined with TB or FB in double-labeling experiments demonstrating the existence of axon collaterals. However, retrograde neuronal labeling with TB or FB requires a relatively long survival time, while NY requires a short survival time since NY migrates rapidly out of the retrogradely labeled neurons. This complicates double-labeling experiments since TB and FB must be injected first and NY later, a short time before the animal is sacrificed. We report a new yellow fluorescent tracer which labels mainly the nucleus and migrates much more slowly out of the retrogradely labeled neurons than NY. This new tracer can be used instead of NY in combination with TB or FB in double-labeling experiments and unlike NY can be injected at the same time as TB or FB. The new tracer is a diamidino compound (no. 28826) which is commercially available. It will be referred to as Diamidino Yellow Dihydrochloride (DY . 2HCl). According to the present study DY . 2HCl is transported over long distances in rat and cat, and produces a yellow fluorescence of the neuronal nucleus at 360 nm excitation wavelength, resembling that obtained with NY. When combined with TB or FB, DY . 2HCl is as effective as NY in double labeling of neurons by way of divergent axon collaterals.

Citing Articles

Layer 1 of somatosensory cortex: an important site for input to a tiny cortical compartment.

Ledderose J, Zolnik T, Toumazou M, Trimbuch T, Rosenmund C, Eickholt B Cereb Cortex. 2023; 33(23):11354-11372.

PMID: 37851709 PMC: 10690867. DOI: 10.1093/cercor/bhad371.


Fluorescent Molecules That Help Reveal Previously Unidentified Neural Connections in Adult, Neonatal and Peripubertal Mammals.

Szabo E, Koves K, Csaki A Int J Mol Sci. 2023; 24(19).

PMID: 37833924 PMC: 10572731. DOI: 10.3390/ijms241914478.


The brainstem connectome database.

Schmitt O, Eipert P, Russ F, Beier J, Kadir K, Horn A Sci Data. 2022; 9(1):168.

PMID: 35414055 PMC: 9005652. DOI: 10.1038/s41597-022-01219-3.


Deciphering neural heterogeneity through cell lineage tracing.

Figueres-Onate M, Sanchez-Gonzalez R, Lopez-Mascaraque L Cell Mol Life Sci. 2020; 78(5):1971-1982.

PMID: 33151389 PMC: 7966193. DOI: 10.1007/s00018-020-03689-3.


Neuroanatomical tract-tracing techniques that did go viral.

Lanciego J, Wouterlood F Brain Struct Funct. 2020; 225(4):1193-1224.

PMID: 32062721 PMC: 7271020. DOI: 10.1007/s00429-020-02041-6.


References
1.
Catsman-Berrevoets C, Kuypers H . A search for corticospinal collaterals to thalamus and mesencephalon by means of multiple retrograde fluorescent tracers in cat and rat. Brain Res. 1981; 218(1-2):15-33. DOI: 10.1016/0006-8993(81)90986-0. View

2.
Huisman A, Kuypers H, Verburgh C . Differences in collateralization of the descending spinal pathways from red nucleus and other brain stem cell groups in cat and monkey. Prog Brain Res. 1982; 57:185-217. DOI: 10.1016/S0079-6123(08)64130-8. View

3.
Flumerfelt B, GWYN D . Proceedings: The red nucleus of the rat: its organization and interconnexions. J Anat. 1974; 118(Pt 2):374, 376. View

4.
Martin G, Cabana T, Humbertson Jr A . Evidence for a lack of distinct rubrospinal somatotopy in the North American opossum and for collateral innervation of the cervical and lumbar enlargements by single rubral neurons. J Comp Neurol. 1981; 201(2):255-63. DOI: 10.1002/cne.902010209. View

5.
Wise S, Jones E . The organization and postnatal development of the commissural projection of the rat somatic sensory cortex. J Comp Neurol. 1976; 168(3):313-43. DOI: 10.1002/cne.901680302. View