نتایج جستجو برای: autologus keratinocyte suspension

تعداد نتایج: 45648  

Journal: :The Journal of craniofacial surgery 2012
David A Leonard Chad R Gordon David H Sachs Curtis L Cetrulo

Fourteen face transplants have been performed worldwide since the procedure was successfully introduced in 2005. Vascularized composite tissue allotransplantation may now be considered a viable option for the repair of complex craniofacial defects, for which the results of autologus reconstruction remain suboptimal. However, the benefits must be balanced against the risks inherent in major surg...

2014
Xupin Jiang Xiaowei Guo Xue Xu Miao Teng Chong Huang Dongxia Zhang Qiong Zhang Jiaping Zhang Yuesheng Huang

Keratinocyte migration is an early event in the wound healing process. Although we previously found that CD9 downregulation is required for the keratinocyte migration during wound repair, the mechanism of how CD9 expression is regulated remains unclear. Here, we observed the effect of hypoxia (2% O2) on CD9 expression and keratinocyte migration. CD9 expression was downregulated and keratinocyte...

2007

The primary goal of post-surgical rehabilitation following cartilage repair (microfracture, grafting, autologus chondrocyte transplantation) is to control pain, reduce inflammation, protect the repaired tissue during the healing process, restore function, improve range-of-motion, and accelerate soft tissue healing. During the initial healing phase following surgery, six to eight weeks4,11,16,25...

2011
Xue Yang Jun Wang Shui-Long Guo Kai-Ji Fan Jun Li You-Liang Wang Yan Teng Xiao Yang

MicroRNAs involved in keratinocyte migration and wound healing are largely unknown. Here, we revealed the indispensable role of miR-21 in keratinocyte migration and in re-epithelialization during wound healing in mice. In HaCaT cell, miR-21 could be upregulated by TGF-β1. Similar to the effect of TGF-β1, miR-21 overexpression promoted keratinocyte migration. Conversely, miR-21 knockdown attenua...

Journal: :The Journal of Cell Biology 1995
N A Hotchin A Gandarillas F M Watt

Integrins of the beta 1 family play a central role in controlling adhesion and terminal differentiation within the epidermis. When human epidermal keratinocytes undergo terminal differentiation, intracellular transport of newly synthesized integrins is inhibited, and mature receptors are lost from the cell surface. We have examined the mechanisms underlying these processes, using an experimenta...

2009
Frances E. Lock Neil A. Hotchin

BACKGROUND The human epidermis is comprised of several layers of specialized epithelial cells called keratinocytes. Normal homoeostasis of the epidermis requires that the balance between keratinocyte proliferation and terminal differentiation be tightly regulated. The mammalian serine/threonine kinases (ROCK1 and ROCK2) are well-characterised downstream effectors of the small GTPase RhoA. We ha...

Journal: :Journal of immunology 2005
Sho Tokumaru Koji Sayama Yuji Shirakata Hitoshi Komatsuzawa Kazuhisa Ouhara Yasushi Hanakawa Yoko Yahata Xiuju Dai Mikiko Tohyama Hiroshi Nagai Lujun Yang Shigeki Higashiyama Akihiko Yoshimura Motoyuki Sugai Koji Hashimoto

The closure of skin wounds is essential for resistance against microbial pathogens, and keratinocyte migration is an important step in skin wound healing. Cathelicidin hCAP18/LL-37 is an innate antimicrobial peptide that is expressed in the skin and acts to eliminate microbial pathogens. Because hCAP18/LL-37 is up-regulated at skin wound sites, we hypothesized that LL-37 induces keratinocyte mi...

2009
Jin A Choi Hyun-Jin Jin Samhyun Jung Eunkyung Yang Jun-Sub Choi So-Hyang Chung Choun-Ki Joo

PURPOSE To investigate the biochemical mechanism of amniotic membrane (AM) suspension on corneal wound healing, particularly on epithelial proliferation and migration. METHODS Human corneal epithelial cells (HCECs) were cultured in media with different concentrations of AM suspension (5% and 30%), Dulbecco's Modified Eagle Medium: Nutrient Mixture F-12 (negative control), and serum containing...

Journal: :CA: A Cancer Journal for Clinicians 2003

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