The entire protocol after cell isolation takes approximately 2 hr.
1. Microsurgical Preparation
<ol>
	<li>Perform stem cell isolation from the donor bone marrow and fluorescent labeling of the isolated subpopulation according to standardized protocols9,12 Allow cells to rest during the time the animal operation is performed. For fluorescent labeling we recommend CFDA (Carboxyfluorescein diacetate succinimidyl ester).</li>
	<li>Anesthetize a male mouse weighing 20-25 g with ketamin...

<ol>
	<li>Madlambayan, G. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=marrow+stem+and+progenitor+cell+contribution+to+neovasculogenesis+is+dependent+on+model+system+with+SDF-1+as+a+permissive+trigger.">marrow stem and progenitor cell contribution to neovasculogenesis is dependent on model system with SDF-1 as a permissive trigger.</a> Blood. 114, 4310-4319 (2009).</li><li>Lapidot, T., Dar, A., Kollet, O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=How+do+stem+cells+find+their+way+home?.">How do stem cells find their way home?.</a> Blood. 106, 1901-1910 (2005).</li><li>Lehr, H. A., Vollmar, B., Vajkoczy, P., Menger, M. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intravital+fluorescence+microscopy+for+the+study+of+leukocyte+interaction+with+platelets+and+endothelial+cells.">Intravital fluorescence microscopy for the study of leukocyte interaction with platelets and endothelial cells.</a> Methods Enzymol. 300, 462-481 (1999).</li><li>Gavins, F. N., Chatterjee, B. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Intravital+microscopy+for+the+study+of+mouse+microcirculation+in+anti-inflammatory+drug+research:+focus+on+the+mesentery+and+cremaster+preparations.">Intravital microscopy for the study of mouse microcirculation in anti-inflammatory drug research: focus on the mesentery and cremaster preparations.</a> J. Pharmacol. Toxicol. Methods. 49, 1-14 (2004).</li><li>Leister, I., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+peritoneal+cavity+chamber+for+intravital+microscopy+of+the+liver+under+conditions+of+pneumoperitoneum.">A peritoneal cavity chamber for intravital microscopy of the liver under conditions of pneumoperitoneum.</a> Surg. Endosc. 17, 939-942 (2003).</li><li>Sriramarao, P., Anderson, W., Wolitzky, B. A., Broide, D. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mouse+bone+marrow-derived+mast+cells+roll+on+P-selectin+under+conditions+of+flow+in+vivo.">Mouse bone marrow-derived mast cells roll on P-selectin under conditions of flow in vivo.</a> Lab Invest. 74, 634-643 (1996).</li><li>Baez, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+open+cremaster+muscle+preparation+for+the+study+of+blood+vessels+by+in+vivo+microscopy.">An open cremaster muscle preparation for the study of blood vessels by in vivo microscopy.</a> Microvasc. Res. 5, 384-394 (1973).</li><li>Bagher, P., Segal, S. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+mouse+cremaster+muscle+preparation+for+intravital+imaging+of+the+microcirculation.">The mouse cremaster muscle preparation for intravital imaging of the microcirculation.</a> J. Vis. Exp. , e2874 (2011).</li><li>Kaminski, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Endothelial+NOS+is+required+for+SDF-1alpha/CXCR4-mediated+peripheral+endothelial+adhesion+of+c-kit++bone+marrow+stem+cells.">Endothelial NOS is required for SDF-1alpha/CXCR4-mediated peripheral endothelial adhesion of c-kit+ bone marrow stem cells.</a> Lab Invest. 88, 58-69 (2008).</li><li>Furlani, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=HMGB-1+induces+c-kit++cell+microvascular+rolling+and+adhesion+via+both+toll-like+receptor-2+and+toll-like+receptor-4+of+endothelial+cells.">HMGB-1 induces c-kit+ cell microvascular rolling and adhesion via both toll-like receptor-2 and toll-like receptor-4 of endothelial cells.</a> J. Cell Mol. Med. 16, 1094-1105 (2012).</li><li>Furlani, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Is+the+intravascular+administration+of+mesenchymal+stem+cells+safe?+Mesenchymal+stem+cells+and+intravital+microscopy.">Is the intravascular administration of mesenchymal stem cells safe? Mesenchymal stem cells and intravital microscopy.</a> Microvasc. Res. 77, 370-376 (2009).</li><li>Donndorf, P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Analysing+migratory+properties+of+human+CD+133(+)+stem+cells+in+vivo+after+intraoperative+sternal+bone+marrow+isolation.">Analysing migratory properties of human CD 133(+) stem cells in vivo after intraoperative sternal bone marrow isolation.</a> Cell Transplant. , (2012).</li></ol>

All animal experiments, conducted for this manuscript have been approved by the local animal care and use committee.
	The authors declare that they have no competing financial interests.

Intravital fluorescence microscopy allows for direct visualization and quantitative analysis of stem cell-endothelium interactions. The cremaster muscle model is particularly useful, since microsurgical exposure and techniques intravital visualization have been well established during the research on leucocyte-endothelium interactions and various chemical components can be selectively applied to the target tissue by simple superfusion technique. Due to the absence of movement artifacts and severe image noise, this partic...

The purpose of the present article is to describe the technique of intravital microscopy (IVM) applied on the mouse cremaster microcirculation for direct observation and analysis of peripheral bone marrow stem cell migration.
The current concept of stem cell based tissue and organ regeneration involves the homing of bone marrow derived stem cells to the injured tissue1. A crucial step for successful stem cell migration includes stem cell interaction with the local endothelium within the injured organ followed by transendothelial migration and eventually organ engraftment2. Intravital analysis of these stem cell - endothelial cell interactions forms an ideal parameter for the quantification of a stem cell based regenerative response in different pathophysiological settings in vivo. Furthermore, it seems conceivable, that, in the future, intravital analysis of the migratory capacity of specific stem cell populations within standardized microcirculatory environments, might be applied prior advancing these populations to further clinical testing.
Intravital microscopy has been initially developed for the observation and quantification of leucocyte-endothelial cell interaction in vivo in the field of inflammatory research3. First successful recordings of intravital microscopy studies were reported by Cohnheim already in the 19th century, studying frogs&#39; tongues and mesenteries under a light microscope4. Since its first use IVM has undergone a tremendous technical development and today certain essential components form prerequisites in order to perform quantitative IVM: (i) tissue preparations that permit optical access, (ii) molecular probes that can be detected by a microscope, (iii) a microscope connected to a detection system and (iv) computer based analysis systems that can extract parameters of interest from the image data set4.
A variety of tissue preparations has been introduced for IVM studies including the mesenteries and liver of the mouse and rat5, the dorsal skinfold chambers of mouse 6 and hamster, the rabbit ear and the hamster cheek pouch to name a few.
However, in the following we will focus on the mouse cremaster muscle, representing an ideal tissue for intravital observations, as preparation and visualization are possible by a well-standardized surgical procedure, and in general no problems of movement artifacts occur. The open cremaster muscle preparation was carried out for the first time in the 1970s by Baez and colleagues 7. Originally described for rats, it has been adopted successfully also to the mouse8. After previous studies had mainly focused on leucocyte interactions with the vessel wall, our own group recently introduced the mouse cremaster muscle preparation as a valuable tool for direct visualization and quantitative analysis of stem cell-endothelium interactions within a defined microenvironment9. Various stem cell subpopulations have been studied utilizing this model, including murine c-kit+ bone marrow stem cell and mesenchymal stem cells, as well as human CD 133+ bone marrow stem cells10-12. Following cell isolation from donor bone marrow and fluorescent labeling for visualization, the stem cells are selectively applied into the cremaster microcirculation utilizing an arterial injection via the femoral artery, thereby avoiding any cell entrapment within remote organs. Furthermore, the cremaster muscle model is particularly useful since various chemokines potentially mediating local stem cell migration within the respective settings, can be topically applied to the target tissue by simple superfusion technique.

<table border="1">
	<tbody>
		<tr>
			<td>Name of Reagent</td>
			<td>Company</td>
			<td>Catalog Number</td>
		</tr>
		<tr>
			<td>Carboxy-fluorescein diacetate succinimidylester (CFDA)</td>
			<td>Invitrogen, Carlsbad, CA, USA</td>
			<td>C1157</td>
		</tr>
		<tr>
			<td>Rhodamine 6 G (1%)</td>
			<td>Sigma-Aldrich, Munich, Germany</td>
			<td>83697</td>
		</tr>
		<tr>
			<td>Ketamin (Ketanest)</td>
			<td>Pfizer, Berlin, Germany</td>
			<td>not available</td>
		</tr>
		<tr>
			<td>Xylacin (Rompun)</td>
			<td>Bayer, Leverkusen, Germany</td>
			<td>not available</td>
		</tr>
		<tr>
			<td>Dulbecco&#39;s Phosphate - buffered saline (PBS)</td>
			<td>PAN Biotech, Aidenbach, Germany</td>
			<td>P04-36500</td>
		</tr>
	</tbody>
</table>

intravital microscopy of the microcirculation in the mouse cremaster muscle for the analysis of peripheral stem cell migration

In the era of intravascular cell application protocols in the context of regenerative cell therapy, the underlying mechanisms of stem cell migration to nonmarrow tissue have not been completely clarified. We describe here the technique of intravital microscopy applied to the mouse cremaster microcirculation for analysis of peripheral bone marrow stem cell migration in vivo. Intravital microscopy of the M. cremaster has been previously introduced in the field of inflammatory research for direct observation of leucocyte interaction with the vascular endothelium. Since sufficient peripheral stem and progenitor cell migration includes similar initial steps of rolling along and firm adhesion at the endothelial lining it is conceivable to apply the M. cremaster model for the observation and quantification of the interaction of intravasculary administered stem cells with the endothelium. As various chemical components can be selectively applied to the target tissue by simple superfusion techniques, it is possible to establish essential microenvironmental preconditions, for initial stem cell recruitment to take place in a living organism outside the bone marrow.

In general, interaction of directly injected stem or progenitor cells with the vascular endothelium within the cremaster muscle microcirculation is a rare event and occurs exclusively in postcapillary venules (diameter: 30-80 &#956;m). Due to fluorescence labeling rolling and firmly adherent stem cells can be clearly quantified in separation from circulating endogenous leucocytes in the observed venules (Figure 2).
The microcirculatory conditions represented by the blood flow ...

Watch this Scientific Journal Video about Intravital Microscopy of the Microcirculation in the Mouse Cremaster Muscle for the Analysis of Peripheral Stem Cell Migration at JoVE.com

Intravital Microscopy of the Microcirculation in the Mouse Cremaster Muscle for the Analysis of Peripheral Stem Cell Migration

Intravital microscopy of the mouse M. cremaster microcirculation offers a unique and well-standardized in vivo model for the analysis of peripheral bone marrow stem cell migration.

In the era of intravascular cell application protocols in the context of regenerative cell therapy, the underlying mechanisms of stem cell migration to ...

intravital-microscopy-microcirculation-mouse-cremaster-muscle-for

Research

JoVE Journal

Biology

15.1K Görüntüleme.  University Rostock.  Fare M. Cremaster'ın mikro intravital mikroskopi eşsiz ve çevresel kemik iliği kök hücre göçü analizi için in vivo model yanı sıra standart sunmaktadır. 