کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1950574 | 1055664 | 2014 | 13 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Notch4 reveals a novel mechanism regulating Notch signal transduction
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
LNRmouse aortic endothelial cellsDll1Notch4Jagged1JAG1ANKTGNEGFIB4raveDelta-like 4DSLdll4 - DLL4Pest - آفاتRetinal angiogenesis - آنژیوژنز شبکیهisolectin B4 - ایزوکتین B4TAD - بلهrapid amplification of cDNA ends - تقویت سریع cDNA به پایان می رسدankyrin repeat - تکرار ankyrinextracellular domain - دامنه خارج سلولیNotch intracellular domain - دامنه درون سلولی NotchTranscriptional activation domain - دامنه فعال سازی رونویسیICD - دفیبریلاتورهای کاردیوورتر کاشتنیdelta-like 1 - دلتا 1numerical aperture - دیافراگم عددیembryonic day - روز جنینیpostnatal day - روز پس از زایمانembryonic stem - ساقه جنینTrans-Golgi network - شبکه Trans-Goljiendoplasmic reticulum - شبکه آندوپلاسمی epidermal growth factor - عامل رشد اپیدرمیCoculture - فرهنگ سازیRace - مسابقه
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شیمی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Notch4 is a divergent member of the Notch family of receptors that is primarily expressed in the vasculature. Its expression implies an important role for Notch4 in the vasculature; however, mice homozygous for the Notch4d1 knockout allele are viable. Since little is known about the role of Notch4 in the vasculature and how it functions, we further investigated Notch4 in mice and in cultured cells. We found that the Notch4d1 allele is not null as it expresses a truncated transcript encoding most of the NOTCH4 extracellular domain. In cultured cells, NOTCH4 did not signal in response to ligand. Moreover, NOTCH4 inhibited signalling from the NOTCH1 receptor. This is the first report of cis-inhibition of signalling by another Notch receptor. The NOTCH4 extracellular domain also inhibits NOTCH1 signalling when expressed in cis, raising the possibility that reported Notch4 phenotypes may not be due to loss of NOTCH4 function. To better address the role of NOTCH4 in vivo, we generated a Notch4 null mouse in which the entire coding region was deleted. Notch4 null mice exhibited slightly delayed vessel growth in the retina, consistent with our novel finding that NOTCH4 protein is expressed in the newly formed vasculature. These findings indicate a role of NOTCH4 in fine-tuning the forming vascular plexus.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Molecular Cell Research - Volume 1843, Issue 7, July 2014, Pages 1272-1284
Journal: Biochimica et Biophysica Acta (BBA) - Molecular Cell Research - Volume 1843, Issue 7, July 2014, Pages 1272-1284
نویسندگان
A.C. James, J.O. Szot, K. Iyer, J.A. Major, S.E. Pursglove, G. Chapman, S.L. Dunwoodie,