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Mesenchymal stem cells recruit macrophages to alleviate experimental colitis through TGFβ1
Liu W, Zhang S, Gu S, Sang L, Dai C (2015) Mesenchymal stem cells recruit macrophages to alleviate experimental colitis through TGFβ1. Cell Physiol Biochem 35:858-865. doi: 10.1159/000369743
Usage: For in vivo depletion of macrophages, mice received i.v. injection of Mac-1-SAP 20 µg, twice per week.
Related Products: Mac-1-SAP mouse/human (Cat. #IT-06)
Investigating the potential of stem cell based therapy in an immunotoxin mouse model of Alzheimer’s disease
Tiwari D, Haynes J, Short J, Pouton C (2014) Investigating the potential of stem cell based therapy in an immunotoxin mouse model of Alzheimer’s disease. Neuroscience 2014 Abstracts 295.14. Society for Neuroscience, Washington, DC.
Summary: Purpose: To characterize a dual reporter embryonic stem (ES) cell line and validate an immunotoxin mouse model of Alzheimer’s disease for future transplantation experiments. Methods: A dual (mcherry and Lhx8+) reporter ES cell line was derived from E14Tg2a mouse ES cells assessed for differentiation capability and characterized using immunocytochemistry. For the immunotoxin model, 6-8 weeks C57BL/6 male mice (n = 12) were treated with bilateral intracerebroventricular injections of saline or mu-p75-saporin toxin (0.4µg/µl/mouse) to cause cholinergic neuronal lesions. Mice were cognitively assessed using a novel water maze (WM) protocol and novel object recognition (NOR) paradigm. Immunohistochemistry was performed to detect toxin dependent neuronal loss. Results: A significant difference in learning the WM task was observed during cued and spatial trials, with toxin-treated mice showing longer latency to platform than controls (two way ANOVA; p<0.01). Also performance during probe trial was significantly reduced in treated mice (t-test; p<0.05), indicating memory loss by toxin. No memory impairment was detected using the NOR test. Immunohistochemistry for choline acetyltransferase (ChAT) confirmed a significant loss (p<0.001; t test) of cholinergic neurons in the medial septum. These data indicate that the model is appropriate for future transplantation studies. FACS analysis of reporter cell line showed a small population of Lhx8+ cells at day 6 and 10 of differentiation. Immunocytochemistry for ChAT on day 18 cells revealed few cholinergic positives neurons as compared to wild type controls. Conclusion: Literature suggests a possible role of Lhx8 in cholinergic development and these cells are being further investigated by transplantation.
Related Products: mu p75-SAP (Cat. #IT-16)
Light-triggered, efficient cytosolic release of IM7-saporin targeting the putative cancer stem cell marker CD44 by photochemical internalization.
Bostad M, Kausberg M, Weyergang A, Olsen C, Berg K, Høgset A, Selbo P (2014) Light-triggered, efficient cytosolic release of IM7-saporin targeting the putative cancer stem cell marker CD44 by photochemical internalization. Mol Pharm 11:2764-2776. doi: 10.1021/mp500129t
Summary: CD44 is known as a common cancer stem cell (CSC) marker. Given that CSC’s seem to have the ability to resist many therapeutic agents, the authors investigated the use of photochemical internalization (PCI) while targeting CD44-expressing CSC’s. An immunotoxin was constructed by biotinylating a pan CD44 antibody and combining it with Streptavidin-ZAP (Cat. #IT-27) at a 4:1 biotinylated antibody to Streptavidin-ZAP molar ratio. Various cancer cell lines were incubated with the toxin at a concentration of 0.825 nM. The toxin showed specific cytotoxicity to CD44-expressing cell lines, demonstrating the efficacy of PCI in conjunction with targeted toxins to treat some cancers
Related Products: Streptavidin-ZAP (Cat. #IT-27), Anti-CD44-SAP (Cat. #IT-72)
Feeder-free derivation of neural crest progenitor cells from human pluripotent stem cells
Zeltner N, Lafaille FG, Fattahi F, Studer L (2014) Feeder-free derivation of neural crest progenitor cells from human pluripotent stem cells. J Vis Exp 87:51609. doi: 10.3791/51609 PMID: 24893703
Related Products: NGFr (ME20.4, p75) Mouse Monoclonal (Cat. #AB-N07)
Microglial VPAC1R mediates a novel mechanism of neuroimmune-modulation of hippocampal precursor cells via IL-4 release.
Nunan R, Sivasathiaseelan H, Khan D, Zaben M, Gray W (2014) Microglial VPAC1R mediates a novel mechanism of neuroimmune-modulation of hippocampal precursor cells via IL-4 release. Glia 62:1313-1327. doi: 10.1002/glia.22682
Summary: Postnatal and adult learning and memory require hippocampal neurogenesis. Cognitive dysfunction is frequently accompanied by neuroinflammatory pathogenesis, but the pathways by which the immune system affects neurogenesis are unclear. In this work the authors depleted microglia from primary hippocampal cultures by incubating the cells with 100 μg/ml Mac-1-SAP rat (Cat. #IT-33) for 24 hours. The hippocampal cells were then washed and cultured for further experiments. It was found that neural stem/progenitor cells had reduced survival and proliferation in cultures treated with Mac-1-SAP. These data sketch out the framework of an immune-neuronal pathway important in the regulation of hippocampal neurogenesis.
Related Products: Mac-1-SAP rat (Cat. #IT-33)
Depletion of alloreactive T cells by anti-CD137-saporin immunotoxin.
Lee SC, Seo KW, Kim HJ, Kang SW, Choi HJ, Kim A, Kwon BS, Cho HR, Kwon B (2015) Depletion of alloreactive T cells by anti-CD137-saporin immunotoxin. Cell Transplant 24:1167-1181. doi: 10.3727/096368914X679327
Summary: The ability to selectively remove T cells that mediate graft-versus-host disease (GVHD) would prevent graft rejection as well as preserve the T cells that mediate graft-versus-leukemia (GVL) effect – especially in cases of hematopoietic stem cell transplantation. In this work the authors used a custom conjugate of anti-mouse CD137 and saporin to eliminate alloreactive T cells during a T cell donor transfer in mice. Rat IgG-SAP (Cat. #IT-17) was used as a control. Transfer of T cells after the immunotoxin treatment did not cause GVHD, but the GVL effect was left intact, indicating the potential of selective T cell depletion for transplantation.
Related Products: Rat IgG-SAP (Cat. #IT-17)
The novel EpCAM-targeting monoclonal antibody 3-17I linked to saporin is highly cytotoxic after photochemical internalization in breast, pancreas and colon cancer cell lines.
Lund K, Bostad M, Skarpen E, Braunagel M, Krauss S, Duncan A, Hogset A, Selbo P (2014) The novel EpCAM-targeting monoclonal antibody 3-17I linked to saporin is highly cytotoxic after photochemical internalization in breast, pancreas and colon cancer cell lines. MAbs 6(4):1038-1050. doi: 10.4161/mabs.28207
Summary: The epithelial cell adhesion molecule (EpCAM) is an attractive diagnostic and therapeutic target for a wide range of human carcinomas. It has also been found on cancer stem cells, increasing the interest in targeting and eliminating cells that express it. The authors have created a monoclonal antibody that binds EpCAM, and use several assays to demonstrate the antibody’s potential as an oncology tool. In one series of assays the biotinylated antibody was combined with streptavidin-ZAP (Cat. #IT-27), and in conjunction with photochemical internalization was shown to have specific cytotoxicity on several different cancer cell lines over a range of concentrations.
Related Products: Streptavidin-ZAP (Cat. #IT-27)
Investigating the potential of stem cell based therapy in an immunotoxin mouse model of Alzheimer’s disease.
Tiwari D, Warden H, Haynes JM, Nicolazzo JA, Pouton CW, Short JL (2013) Investigating the potential of stem cell based therapy in an immunotoxin mouse model of Alzheimer’s disease. Neuroscience 2013 Abstracts 712.19. Society for Neuroscience, San Diego, CA.
Summary: Purpose: Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by reduced cognitive function. Stem cell based therapeutic approaches are a potential therapeutic option. In order to investigate this possibility the study focuses on the characterization of a dual reporter embryonic stem (ES) cell line and validation of an immunotoxin mouse model of AD for future transplantation experiments. Methods: A dual (mcherry and Lhx8+) reporter ES cell line was derived from the E14Tg2a mouse ES cell line. The ES cells were assessed for their differentiation capability and characterized using mmunocytochemistry. For the immunotoxin model, 6-8 week old C57BL/6 male mice (n = 12) were treated with bilateral intracerebroventricular injections of saline (control) or mu-p75-saporin toxin (0.4µg/µl/mouse) to cause cholinergic neuronal lesions. Mice were cognitively assessed using a novel three day water maze (WM) protocol and the novel object recognition (NOR) paradigm. Immunohistochemistry was done to detect the toxin dependent loss of cholinergic neurons. Results and conclusions: A significant difference in learning the WM task was observed during cued and spatial trials, with toxin-treated mice taking longer to reach the platform than control mice (two way ANOVA; p<0.01). Performance in the WM during the probe trial was also significantly reduced in toxin-treated mice, compared to control mice (t-test; p<0.05), indicating memory loss in toxin-injected mice and better learning in the saline-treated controls. However, no memory impairment was detected using the NOR test. Immunohistochemistry for choline acetyltransferase (ChAT) confirmed a significant loss (p<0.0001; t test) of cholinergic neurons in the medial septum. These data indicate that the toxin model is appropriate for use in subsequent transplantation studies. FACS analysis of the reporter cell line showed the presence of a small population of Lhx8+ cells at day 6 and 10 of differentiation. Immunocytochemistry for ChAT on day 18 cells revealed the presence of a few cholinergic positives neurons as compared to wild type controls. Literature suggests a possible role of Lhx8 in cholinergic development and these cells will be investigated further in order to select cholinergic progenitors for transplantation.
Related Products: mu p75-SAP (Cat. #IT-16)
Featured Article: Medial ganglionic eminence-like cells derived from human embryonic stem cells correct learning and memory deficits in an NGFr-lesioned mouse model
Liu Y, Weick JP, Liu H, Krencik R, Zhang X, Ma L, Zhou GM, Ayala M, Zhang S (2013) Featured Article: Medial ganglionic eminence-like cells derived from human embryonic stem cells correct learning and memory deficits in an NGFr-lesioned mouse model. Targeting Trends 14(3)
Related Products: mu p75-SAP (Cat. #IT-16)
Read the featured article in Targeting Trends.
See Also:
A robust method to derive functional neural crest cells from human pluripotent stem cells
Kreitzer FR, Salomonis N, Sheehan A, Huang M, Park JS, Spindler MJ, Lizarraga P, Weiss WA, So PL, Conklin BR (2013) A robust method to derive functional neural crest cells from human pluripotent stem cells. Am J Stem Cells 2(2):119-131. PMID: 23862100
Usage: Immunocytochemistry 1:200
Related Products: NGFr (ME20.4, p75) Mouse Monoclonal (Cat. #AB-N07)