By Robert M Hoffman
This quantity discusses equipment for the learn of multipotent and pluripotent stem cells of the hair follicle. The stem cells defined are inquisitive about either the expansion of the hair follicle and its construction of the hair shaft, in addition to the expansion of the hair follicle sensory nerve. Multipotent Stem Cells of the Hair Follicle: tools and Protocols additionally explores very unforeseen effects corresponding to that of the hair follicle-associated-pluripotent (HAP) stem cells, which not just have the aptitude for regenerating the hair follicle sensory nerve, but in addition can differentiate ex vivo and in vivo to a number of mobilephone forms now not linked to the hair follicle―these comprise glial cells, motor neurons, and beating cardiac muscle cells. the potential of HAP stem cells for regenerative medication is usually mentioned intimately. Written within the hugely profitable Methods in Molecular Biology series layout, chapters comprise introductions to their respective issues, lists of the required fabrics and reagents, step by step, effortlessly reproducible laboratory protocols, and tips about troubleshooting and heading off recognized pitfalls.
Cutting-edge and thorough, Multipotent Stem Cells of the Hair Follicle: equipment and Protocols is a useful source for researchers attracted to this field.
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Additional resources for Multipotent Stem Cells of the Hair Follicle: Methods and Protocols
Then change the medium to serumfree culture medium. Culture for another 7 days. 4 Preparation of Scaffold 1. Harvest beagle sciatic nerves from another experiment that has no effect on nerve tissues. Cut the nerves into 4 cm segments. 2. 3, for 5 days at 4 °C. 01 M PBS at room temperature for 4 days. Change the incubation solution every 24 h. For the last 2 days, supplement the solution with 10 mM CaCl2. 3. Wash the extracted nerve segments in CMF-PBS for 30 min and incubate them in CMF-PBS supplemented with 600 U/ml DNase I and 10 U/ml RNase A at 37 °C for 24 h.
Open the wound 1 week later and remove the whisker pad, including the injured trigeminal nerve, and observe microscopically with an MVX-10 microscope. 6 Confocal Laser Scanning Microscopy 1. Use a FV1000 confocal laser scanning microscope for two(X,Y) and three-dimensional (3D, X,Y,Z) high-resolution imaging of vibrissa follicles and nerves in histoculture. Obtain 44 Sumiyuki Mii et al. Fig. 2 A skin-flap is made to visualize the whisker pad and trigeminal nerve Fig. 00w XLUMplan FL objectives.
References 1. Xu L, Zhou S, Feng GY et al (2012) Neural stem cells enhance nerve regeneration after sciatic nerve injury in rats. Mol Neurobiol 46(2):265–274 2. Uemura T, Takamatsu K, Ikeda M et al (2012) Transplantation of induced pluripotent stem cell-derived neurospheres for peripheral nerve repair. Biochem Biophys Res Commun 419(1):130–135 3. Liu BS, Yang YC, Shen CC (2012) Regenerative effect of adipose tissue-derived stem cells transplantation using nerve conduit therapy on sciatic nerve injury in rats.