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1.
Wound Repair Regen ; 21(4): 512-9, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23755915

RESUMO

Undermining is one of the most challenging complications of deep pressure ulcers. Recommendations in most guidelines are based only on expert opinions. Here, we examined the relationship between surgical incision of the undermined space and pressure ulcer healing through a Japanese multicenter prospective cohort study. A total of 162 patients with undermining in 40 national hospitals in Japan were enrolled from July 2007 to June 2009. The incision group included 39 patients (24.1%) whose undermining was surgically incised during the observational period. Their 4-week follow-up data on pressure ulcer severity and areas of healthy granulation tissue were recorded as outcome variables using the DESIGN-R pressure ulcer assessment tool. The 4-week follow-up was restarted after the incision in the incision group. The outcome variables over time were compared between the two groups using a linear mixed model with or without adjustment for demographic and other variables. The incision group showed more rapid improvement in the total and granulation DESIGN-R scores compared with the nonincision group (p < 0.001 and p = 0.007, respectively, in the crude models). This study may provide the first considerable evidence to support that surgical incision of undermining may promote healing of deep pressure ulcers.


Assuntos
Úlcera por Pressão/cirurgia , Idoso , Idoso de 80 Anos ou mais , Estudos de Coortes , Feminino , Humanos , Japão , Masculino , Pessoa de Meia-Idade , Úlcera por Pressão/patologia , Estudos Prospectivos , Resultado do Tratamento , Cicatrização
2.
Nat Commun ; 11(1): 5645, 2020 11 06.
Artigo em Inglês | MEDLINE | ID: mdl-33159086

RESUMO

The formation of hair follicles, a landmark of mammals, requires complex mesenchymal-epithelial interactions and it is commonly believed that embryonic epidermal cells are the only cells that can respond to hair follicle morphogenetic signals in vivo. Here, we demonstrate that epithelial stem cells of non-skin origin (e.g. that of cornea, oesophagus, vagina, bladder, prostate) that express the transcription factor Tp63, a master gene for the development of epidermis and its appendages, can respond to skin morphogenetic signals. When exposed to a newborn skin microenvironment, these cells express hair-follicle lineage markers and contribute to hair follicles, sebaceous glands and/or epidermis renewal. Our results demonstrate that lineage restriction is not immutable and support the notion that all Tp63-expressing epithelial stem cells, independently of their embryonic origin, have latent skin competence explaining why aberrant hair follicles or sebaceous glands are sometimes observed in non-skin tissues (e.g. in cornea, vagina or thymus).


Assuntos
Células Epidérmicas/metabolismo , Epiderme/metabolismo , Folículo Piloso/metabolismo , Células-Tronco/metabolismo , Transativadores/metabolismo , Animais , Epiderme/crescimento & desenvolvimento , Feminino , Humanos , Masculino , Camundongos , Ratos , Transativadores/genética
3.
Congenit Anom (Kyoto) ; 46(3): 129-34, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16922919

RESUMO

This review describes culture techniques for the epithelial system as well as trends in the clinical application of cultured keratinocytes in our department and the possibility of applying the techniques to other organs. Cultured epithelium and cultured dermis in particular have considerably preceded regeneration of other organs in the field of regenerative medicine. Since 1988 we have grafted cultured keratinocytes by the Rheinwald-Green modified method in at least 500 patients with large skin defects. As a result of the establishment of a culture technique for individual patients, it is now possible to prepare enough regenerated epithelium to cover the body surface area of as many as 10 adult patients in approximately three weeks after collecting 1 cm(2) of skin, and then remaining cultured keratinocytes can be cryo-preserved for two-stage dermatoplasty at another site. This procedure makes it possible to avoid frequent skin collection from the same patient and thereby improves patients' quality of life and activities of daily living. On the other hand, to solve the problem of regenerated epithelium shrinking and problems with graft efficiency on dermis defect lesion, we have developed a proteinase-resistant regenerated dermis by mixing a certain protein with a fibrin scaffold. Recently we also took the initiative in grafting hybrid-type regenerated trachea in an animal experiment by using the epithelial and dermal cell culture technique, and some results of the graft were obtained.


Assuntos
Técnicas de Cultura de Células , Células Epiteliais/citologia , Células Epiteliais/transplante , Queratinócitos/transplante , Transplante de Pele/métodos , Animais , Procedimentos Cirúrgicos Dermatológicos , Humanos , Queratinócitos/citologia , Peptídeo Hidrolases/metabolismo , Células-Tronco/citologia
4.
Hum Cell ; 15(3): 118-28, 2002 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-12703542

RESUMO

The technique of epidermal cell culture developed by Green and colleagues made a breakthrough in the treatment of massive wounds in vivo with grown cells in vitro. In the past two decades, progress of culture methods and clinical practice have been made and now it is possible to treat extensive skin defect with large amounts of cultured epithelium. Since 1985, we have been successfully used cultured epidermis as autografts for the permanent coverage of full-thickness burn wounds or excised burn scars, giant nevi, tattoos and so on. Furthermore, cultured epidermis has been available as allografts to promote the healing of chronic skin ulcers or deep dermal burn. In this paper we describe our clinical experience of cultured epithelium grafting for the treatment of wounds and predict new trial of wound management and regeneration based on tissue engineering concept.


Assuntos
Queimaduras/cirurgia , Técnicas de Cultura de Células/métodos , Procedimentos Cirúrgicos Dermatológicos , Células Epiteliais/transplante , Células-Tronco , Engenharia Tecidual , Cicatrização/fisiologia , Adulto , Células Cultivadas , Criança , Pré-Escolar , Humanos , Masculino , Tatuagem , Vitiligo/cirurgia
5.
Chemistry ; 13(27): 7745-52, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17605154

RESUMO

Amyloid beta-peptide (Abeta) plays a critical role in Alzheimer's disease (AD). The monomeric state of Abeta can self-assemble into oligomers, protofibrils, and amyloid fibrils. Since the fibrils and soluble oligomers are believed to be responsible for AD, the construction of molecules capable of capturing these species could prove valuable as a means of detecting these potentially toxic species and of providing information pertinent for designing drugs effective against AD. To this aim, we have designed short peptides with various hydrophobicities based on the sequence of Abeta14-23, which is a critical region for amyloid fibril formation. The binding of the designed peptides to Abeta and the amplification of the formation of peptide amyloid-like fibrils coassembled with Abeta are elucidated. A fluorescence assay utilizing thioflavin T, known to bind specifically to amyloid fibrils, revealed that two designed peptides (LF and VF, with the leucine and valine residues, respectively, in the hydrophobic core region) could form amyloid-like fibrils effectively by using mature Abeta1-42 fibrils as nuclei. Peptide LF also coassembled with soluble Abeta oligomers into peptide fibrils. Various analyses, including immunostaining with gold nanoparticles, enzyme-linked immunosorbent assays, and size-exclusion chromatography, confirmed that the LF and VF peptides formed amyloid-like fibrils by capturing and incorporating Abeta1-42 aggregates into their peptide fibrils. In this system, small amounts of mature Abeta1-42 fibrils or soluble oligomers could be transformed into peptide fibrils and detected by amplifying the amyloid-like fibrils with the designed peptides.


Assuntos
Peptídeos beta-Amiloides/química , Fragmentos de Peptídeos/química , Peptídeos/química , Sequência de Aminoácidos , Cromatografia em Gel , Cromatografia Líquida de Alta Pressão , Dicroísmo Circular , Ensaio de Imunoadsorção Enzimática , Microscopia Eletrônica de Transmissão , Espectrometria de Fluorescência , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz
6.
Proc Natl Acad Sci U S A ; 102(41): 14677-82, 2005 Oct 11.
Artigo em Inglês | MEDLINE | ID: mdl-16203973

RESUMO

Adult stem cells are essential for tissue renewal, regeneration, and repair, and their expansion in culture is of paramount importance for regenerative medicine. Using the whisker follicle of the rat as a model system, we demonstrate that (i) clonogenicity is an intrinsic property of the adult stem cells of the hair follicle; (ii) after cultivation for >140 doublings, these stem cells, transplanted to the dermo-epidermal junction of newborn mouse skin, form part or all of the developing follicles; (iii) the stem cells incorporated into follicles are multipotent, because they generate all of the lineages of the hair follicle and sebaceous gland; (iv) thousands of hair follicles can be generated from the progeny of a single cultivated stem cell; (v) cultured stem cells express the self-renewal genes Bmi1 and Zfp145;(vi) several stem cells participate in the formation of a single hair bulb; and (vii) there are many more stem cells in whisker follicles than could be anticipated from label-retaining experiments.


Assuntos
Folículo Piloso/fisiologia , Células-Tronco Multipotentes/citologia , Células-Tronco Multipotentes/metabolismo , Regeneração/fisiologia , Animais , Primers do DNA , Folículo Piloso/citologia , Hibridização in Situ Fluorescente , Proteínas Nucleares/metabolismo , Complexo Repressor Polycomb 1 , Proteínas Proto-Oncogênicas/metabolismo , Ratos , Ratos Endogâmicos F344 , Proteínas Repressoras/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Transplante de Células-Tronco/métodos , Dedos de Zinco/genética
7.
J Immunol ; 174(3): 1357-64, 2005 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-15661893

RESUMO

The inability to reproducibly induce robust and durable transplant tolerance using CD28-B7 pathway blockade is in part related to the persistence of alloreactive effector/memory CD8(+) T cells that are less dependent on this pathway for their cellular activation. We studied the role of the novel T cell costimulatory pathway, CD27-CD70, in alloimmunity in the presence and absence of CD28-B7 signaling. CD70 blockade prolonged survival of fully mismatched vascularized cardiac allografts in wild-type murine recipients, and in CD28-deficient mice induced long-term survival while significantly preventing the development of chronic allograft vasculopathy. CD70 blockade had little effect on CD4(+) T cell function but prevented CD8(+) T cell-mediated rejection, inhibited the proliferation and activation of effector CD8(+) T cells, and diminished the expansion of effector and memory CD8(+) T cells in vivo. Thus, the CD27-CD70 pathway is critical for CD28-independent effector/memory CD8(+) alloreactive T cell activation in vivo. These novel findings have important implications for the development of transplantation tolerance-inducing strategies in primates and humans, in which CD8(+) T cell depletion is currently mandatory.


Assuntos
Antígenos CD/fisiologia , Antígenos CD28/fisiologia , Linfócitos T CD8-Positivos/imunologia , Transplante de Coração/imunologia , Proteínas de Membrana/fisiologia , Transdução de Sinais/imunologia , Transplante Heterotópico/imunologia , Doença Aguda , Transferência Adotiva , Animais , Anticorpos Bloqueadores/administração & dosagem , Anticorpos Monoclonais/administração & dosagem , Antígenos CD/imunologia , Ligante CD27 , Antígenos CD28/genética , Linfócitos T CD4-Positivos/imunologia , Linfócitos T CD4-Positivos/transplante , Doença Crônica , Regulação para Baixo/imunologia , Rejeição de Enxerto/genética , Rejeição de Enxerto/imunologia , Sobrevivência de Enxerto/genética , Sobrevivência de Enxerto/imunologia , Memória Imunológica/imunologia , Isoanticorpos/biossíntese , Isoanticorpos/sangue , Células Matadoras Naturais/imunologia , Ativação Linfocitária/imunologia , Proteínas de Membrana/antagonistas & inibidores , Proteínas de Membrana/imunologia , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BL , Camundongos Knockout , Camundongos Mutantes , Camundongos Transgênicos , Linfócitos T Citotóxicos/imunologia , Linfócitos T Citotóxicos/metabolismo , Células Th1/imunologia , Células Th1/metabolismo , Células Th2/imunologia , Células Th2/metabolismo , Membro 7 da Superfamília de Receptores de Fatores de Necrose Tumoral/fisiologia , Regulação para Cima/imunologia
8.
Nature ; 416(6883): 854-60, 2002 Apr 25.
Artigo em Inglês | MEDLINE | ID: mdl-11976685

RESUMO

Stem cells which have the capacity to self-renew and generate differentiated progeny are thought to be maintained in a specific environment known as a niche. The localization of the niche, however, remains largely obscure for most stem-cell systems. Melanocytes (pigment cells) in hair follicles proliferate and differentiate closely coupled to the hair regeneration cycle. Here we report that stem cells of the melanocyte lineage can be identified, using Dct-lacZ transgenic mice, in the lower permanent portion of mouse hair follicles throughout the hair cycle. It is only the population in this region that fulfils the criteria for stem cells, being immature, slow cycling, self-maintaining and fully competent in regenerating progeny on activation at early anagen (the growing phase of hair follicles). Induction of the re-pigmentation process in K14-steel factor transgenic mice demonstrates that a portion of amplifying stem-cell progeny can migrate out from the niche and retain sufficient self-renewing capability to function as stem cells after repopulation into vacant niches. Our data indicate that the niche has a dominant role in the fate determination of melanocyte stem-cell progeny.


Assuntos
Diferenciação Celular , Linhagem da Célula , Folículo Piloso/citologia , Melanócitos/citologia , Células-Tronco/citologia , Animais , Divisão Celular , Movimento Celular , Genes Reporter/genética , Cor de Cabelo , Folículo Piloso/metabolismo , Imuno-Histoquímica , Melanócitos/metabolismo , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Transgênicos , Proteínas Oncogênicas/fisiologia , Proteínas Proto-Oncogênicas c-kit , Células-Tronco/metabolismo
9.
J Investig Dermatol Symp Proc ; 8(1): 28-38, 2003 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12894992

RESUMO

The workshop on Hair Follicle Stem Cells brought together investigators who have used a variety of approaches to try to understand the biology of follicular epithelial stem cells, and the role that these cells play in regulating the hair cycle. One of the main concepts to emerge from this workshop is that follicular epithelial stem cells are multipotent, capable of giving rise not only to all the cell types of the hair, but also to the epidermis and the sebaceous gland. Furthermore, such multipotent stem cells may represent the ultimate epidermal stem cell. Another example of epithelial stem cell and transit amplifying cell plasticity, was the demonstration that adult corneal epithelium, under the influence of embryonic skin dermis could form an epidermis as well as hair follicles. With regards to the location of follicular epithelial stem cells, immunohistochemical and ultrastructural data was presented, indicating that cells with stem cell attributes were localized to the prominent bulge region of developing human fetal hair follicles. Finally, a new notion was put forth concerning the roles that the bulge-located stem cells and the hair germ cells played with respect to the hair cycle.


Assuntos
Folículo Piloso/fisiologia , Células-Tronco/fisiologia , Animais , Embrião de Mamíferos/fisiologia , Epiderme/embriologia , Epiderme/fisiologia , Epitélio Corneano/citologia , Epitélio Corneano/fisiologia , Folículo Piloso/citologia , Folículo Piloso/embriologia , Folículo Piloso/crescimento & desenvolvimento , Humanos , Modelos Biológicos , Pele/crescimento & desenvolvimento
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