References

Hawryluk JM, Ferrari LL, Keating SA, Arrigoni E (2012) Adenosine inhibits glutamatergic input to basal forebrain cholinergic neurons. J Neurophysiol 107(10):2769-2781. doi: 10.1152/jn.00528.2011 PMID: 22357797

Summary: Using patch-clamp recordings from mouse brain slices the authors demonstrate that adenosine not only directly inhibits cholinergic neurons in the basal forebrain, it also reduces excitatory inputs to these neurons as well. Cy3-anti-mu p75 (Cat. #FL-05, 40-60 ng) was injected into the lateral cerebroventricle.

Related Products: NGFr (mu p75) Rabbit Polyclonal, affinity-purified Cy3-labeled (Cat. #AB-N01APFL3)

Kanju PM, Parameshwaran K, Sims-Robinson C, Uthayathas S, Josephson EM, Rajakumar N, Dhanasekaran M, Suppiramaniam V (2012) Selective cholinergic depletion in medial septum leads to impaired long term potentiation and glutamatergic synaptic currents in the hippocampus. PLoS One 7(2):e31073. doi: 10.1371/journal.pone.0031073

Summary: Long term potentiation (LTP) is dependent on excitatory neurotransmission in the hippocampus, which plays a major role in learning and memory. The authors examine whether cholinergic lesions in the medial septum result in LTP alteration or affect synaptic glutamate receptor subtypes. After bilateral administration of 192-IgG-SAP (Cat. #IT-01, 50 ng per injection) into the medial septum of rats, hippocampal slices were made and the LTP of the slices was measured. The data show modulation of medial septal LTP and hippocampal glutaminergic currents by cholinergic afferents.

Related Products: 192-IgG-SAP (Cat. #IT-01)

Han N, Zu JY, Chai J (2012) Spinal bombesin-recognized neurones mediate more nonhistaminergic than histaminergic sensation of itch in mice. Clin Exp Dermatol 37(3):290-295. doi: 10.1111/j.1365-2230.2011.04314.x

Summary: The authors administered 400 ng of Bombesin-SAP (Cat. #IT-40) to the lumbar spinal subarachnoid space of rats and evaluated the distribution of Fos-positive cells in the dorsal horn after stimulation. Saporin (Cat. #PR-01) was used as a control. The results demonstrate that the neurons eliminated by Bombesin-SAP are critical to both acute and chronic itch pathways, although they have more effect on nonhistaminergic sensation.

Related Products: Bombesin-SAP (Cat. #IT-40), Saporin (Cat. #PR-01)

Rothenberg ME, Nusse Y, Kalisky T, Lee JJ, Dalerba P, Scheeren F, Lobo N, Kulkarni S, Sim S, Qian D, Beachy PA, Pasricha PJ, Quake SR, Clarke MF (2012) Identification of a cKit(+) colonic crypt base secretory cell that supports Lgr5(+) stem cells in mice. Gastroenterology 142:1195-1205.e1196. doi: 10.1053/j.gastro.2012.02.006

Objective: To investigate the existence of colonic Paneth-like cells that have a distinct transcriptional signature and support Lgr5 stem cells.

Summary: cKit marks small intestinal Paneth cells and a subset of colonic goblet cells that are regulated by Notch signaling and support Lgr5+ stem cells.

Usage: For saporin experiments, small intestinal organoids with crypt buds and visible Paneth cells were passaged as single cells. Before embedding in Matrigel, dissociated cells were incubated with Anti-cKit-SAP (biotinylated-2B8 mixed with Streptavidin-ZAP). Treatment led to a marked decrease in organoid formation.

Related Products: Streptavidin-ZAP (Cat. #IT-27)

Selbo PK, Weyergang A, Eng MS, Bostad M, Maelandsmo GM, Hogset A, Berg K (2012) Strongly amphiphilic photosensitizers are not substrates of the cancer stem cell marker ABCG2 and provides specific and efficient light-triggered drug delivery of an EGFR-targeted cytotoxic drug. J Control Release 159(2):197-203. doi: 10.1016/j.jconrel.2012.02.003

Summary: Many anti-cancer drugs are substrates of the ATP-binding cassette transporter ABCG2. Unfortunately ABCG2 is also thought to play an important role in multi-drug resistance and the protection of cancer stem cells against chemotherapeutics and photodynamic therapy. This paper examined whether photosensitizers used in photochemical internalization (PCI) are substrates for ABCG2. Streptavidin-ZAP (Cat. #IT-27) was combined with biotinylated EGF and applied to cells in culture; saporin (Cat. #PR-01) was used as a control. The data show that PCI with the EGF-saporin toxin did not utilize ABCG2 to enter cells.

Related Products: Streptavidin-ZAP (Cat. #IT-27), Saporin (Cat. #PR-01)

Antonucci F, Alpár A, Kacza J, Caleo M, Verderio C, Giani A, Martens H, Chaudhry FA, Allegra M, Grosche J, Michalski D, Erck C, Hoffmann A, Harkany T, Matteoli M, Härtig W (2012) Cracking down on inhibition: Selective removal of GABAergic interneurons from hippocampal networks. J Neurosci 32(6):1989-2001. doi: 10.1523/JNEUROSCI.2720-11.2012

Related Products: Anti-vGAT-SAP (Cat. #IT-71)

Gibbons DD, Southerland EM, Hoover DB, Beaumont E, Armour JA, Ardell JL (2012) Neuromodulation targets intrinsic cardiac neurons to attenuate neuronally mediated atrial arrhythmias. Am J Physiol Regul Integr Comp Physiol 302(3):R357-R364. doi: 10.1152/ajpregu.00535.2011 PMID: 22088304

Summary: Cardiac arrhythmias can be generated by excessive activation of specific inputs to the intrinsic cardiac nervous system. The authors sought to determine whether subpopulations of neurons were responsible for this activation, and therefore potential therapeutic targets. A series of studies were done following electrical stimuli to the mediastinal nerves. Choline acetyltransferase levels were assessed using anti-ChAT (Cat. #AB-N34) in immunohistochemistry. The data suggest activation of certain neurons by mediastinal nerve stimulation results in atrial arrhythmias leading to atrial fibrillation.

Related Products: Choline Acetyltransferase Rabbit Polyclonal (Cat. #AB-N34)

Minami SS, Sun B, Popat K, Kauppinen T, Pleiss M, Zhou Y, Ward ME, Floreanig P, Mucke L, Desai T, Gan L ( 2012 ) Selective targeting of microglia by quantum dots. J Neuroinflammation 9(1):22 . doi: 10.1186/1742-2094-9-22

Related Products: MonoBiotin-ZAP (Cat. #BT-ZAP)

Kobets AJ (2012) Vector-mediated gene delivery to model striatal interneuron loss in sever tourette syndrome. Yale Univ School and Medicine Thesis.

Objective: Develop a viral-mediated gene delivery technique to selectively ablate striatal interneurons in mice to model the pathophysiology of Tourette syndrome (TS).

Summary: The loss of striatal interneurons was speculated to play a role in TS. In order to model the pathophysiology of TS, the author used adeno-associated virus (AAV) gene therapy to ablate striatal interneurons in mice and perform behavioral analyses. As a comparison tool to help strengthen the results, mice were also lesioned with Anti-ChAT-SAP (IT-42) to lesion neurons expressing choline acetyl-transferase, the same neurons affected by the gene therapy.

Usage: Anti-ChAT-SAP (IT-42) was unilaterally injected into the brain of wild type mice.

Related Products: Anti-ChAT-SAP (Cat. #IT-42)

Choi JI, Koehrn FJ, Sorkin LS (2012) Carrageenan induced phosphorylation of Akt is dependent on neurokinin-1 expressing neurons in the superficial dorsal horn. Mol Pain 8(1):4. doi: 10.1186/1744-8069-8-4 PMID: 22243518

Summary: In this work the authors administered 100 ng SSP-SAP (Cat. #IT-11) into the intrathecal space of rats (saporin, Cat. #PR-01, was used as a control). Lesioned animals displayed decreased carrageenan-induced mechanical allodynia, and carrageenan-induced phosphorylation of Akt was blocked throughout the spinal cord gray matter. Anti-NK-1 (Cat. #AB-N33AP) was used for immunohistochemistry.

Related Products: SSP-SAP (Cat. #IT-11), Saporin (Cat. #PR-01), NK-1 Receptor Rabbit Polyclonal, affinity-purified (Cat. #AB-N33AP)