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	<title>Talk:Muscle Development - Revision history</title>
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	<updated>2026-11-02T01:42:03Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<title>Z8600021: Created page with &quot;{{Talk Page}}  ==2012==  ===Differentiation of vascular smooth muscle cells from local precursors during embryonic and adult arteriogenesis requires Notch signaling=== Proc Na...&quot;</title>
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		<updated>2012-05-03T03:05:01Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;{{Talk Page}}  ==2012==  ===Differentiation of vascular smooth muscle cells from local precursors during embryonic and adult arteriogenesis requires Notch signaling=== Proc Na...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Talk Page}}&lt;br /&gt;
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==2012==&lt;br /&gt;
&lt;br /&gt;
===Differentiation of vascular smooth muscle cells from local precursors during embryonic and adult arteriogenesis requires Notch signaling===&lt;br /&gt;
Proc Natl Acad Sci U S A. 2012 May 1;109(18):6993-6998. Epub 2012 Apr 16.&lt;br /&gt;
&lt;br /&gt;
Chang L, Noseda M, Higginson M, Ly M, Patenaude A, Fuller M, Kyle AH, Minchinton AI, Puri MC, Dumont DJ, Karsan A.&lt;br /&gt;
Source&lt;br /&gt;
Genome Sciences Centre, Integrative Oncology Department, and Cancer Genetics Laboratory, British Columbia Cancer Agency, Vancouver, BC, Canada V5Z 1L3.&lt;br /&gt;
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Abstract&lt;br /&gt;
&lt;br /&gt;
Vascular smooth muscle cells (VSMC) have been suggested to arise from various developmental sources during embryogenesis, depending on the vascular bed. However, evidence also points to a common subpopulation of vascular progenitor cells predisposed to VSMC fate in the embryo. In the present study, we use binary transgenic reporter mice to identify a Tie1(+)CD31(dim)vascular endothelial (VE)-cadherin(-)CD45(-) precursor that gives rise to VSMC in vivo in all vascular beds examined. This precursor does not represent a mature endothelial cell, because a VE-cadherin promoter-driven reporter shows no expression in VSMC during murine development. Blockade of Notch signaling in the Tie1(+) precursor cell, but not the VE-cadherin(+) endothelial cell, decreases VSMC investment of developing arteries, leading to localized hemorrhage in the embryo at the time of vascular maturation. However, Notch signaling is not required in the Tie1(+) precursor after establishment of a stable artery. Thus, Notch activity is required in the differentiation of a Tie1(+) local precursor to VSMC in a spatiotemporal fashion across all vascular beds.&lt;br /&gt;
&lt;br /&gt;
PMID 22509029&lt;/div&gt;</summary>
		<author><name>Z8600021</name></author>
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