RESUMO
Non-healing skin wounds remain a challenge in the healthcare system. In this sense, it is suggested that the secretome of mesenchymal stromal cells (MSCs) can be effective as a therapeutic strategy for regenerative medicine. Therefore, this systematic review aimed to determine the effects of treatment with a secretome derived from MSCs on the healing of skin wounds in a preclinical model of rodents (mice and rats). Studies were systematically retrieved from 6 databases and gray literature that provided 1,172 records, of which 25 met the inclusion criteria for qualitative analysis. Results revealed substantial heterogeneity among studies concerning experimental designs and methodologies, resulting in a high risk of bias. Together, the selected studies reported that treatment improved wound healing by (1) accelerating wound closure and improving skin repair quality; (2) reducing inflammation by decreasing the number of cells and inflammatory cytokines, accompanied by polarization of the M2 macrophage; (3) complete re-epithelialization and epidermal reorganization; (4) neovascularization promoted by proliferation of endothelial cells (CD34+) and increased levels of pro-angiogenic mediators; (5) better scar quality promoted by increased expression of collagen types I and III, as well as improved deposition and remodeling of collagen fibers. In conclusion, despite the need for alignment of methodological protocols and transparent reports in future studies, results show that the secretome of MSCs from different tissue sources corresponds to a promising tool of regenerative medicine for the treatment of skin wounds.
Assuntos
Transplante de Células-Tronco Mesenquimais , Células-Tronco Mesenquimais , Ratos , Camundongos , Animais , Células Endoteliais , Secretoma , Pele/lesões , Cicatrização , Colágeno , Transplante de Células-Tronco Mesenquimais/métodosRESUMO
Chromaffin granules isolated from adrenal glands constitute a powerful experimental tool to the study of secretory vesicle components and their participation in fusion and docking processes, vesicle aggregation, and interactions with cytosolic components. Although it is possible to isolate and purify chromaffin granules from adrenal glands of different species, bovine adrenal glands are the most used tissue source due to its easy handling and the large amount of granules that can be obtained from this tissue. In this chapter, we describe an easy-to-use and short-term protocol for efficiently obtaining highly purified chromaffin granules from bovine adrenal medulla. We additionally include protocols to isolate granules from cultured bovine chromaffin cells and PC12 cells, as well as a section to obtain chromaffin granules from mouse adrenal glands.
Assuntos
Medula Suprarrenal , Células Cromafins , Células Neuroendócrinas , Glândulas Suprarrenais , Animais , Bovinos , Grânulos Cromafim , Camundongos , Células PC12 , RatosRESUMO
The cardiac atria secrets polypeptide hormones usually called natriuretic peptides (NPs). These substances play a relevant role in the blood pressure regulation. The objective of the study was to estimate the effects of aging on the secretory apparatus of NPs in cardiomyocytes of the right atrium. Twenty male Wistar rats were studied: 10 young animals aged 3 months old (237⯱â¯27â¯g; mean⯱â¯SD) and 10 old animals aged 20 months old (450⯱â¯68â¯g; mean⯱â¯SD). The systolic blood pressure was verified instants before the moment of the euthanasia. Electron micrographs were prepared to quantify the area and density of the NP granules and the relative volumes of the endoplasmic reticulum, Golgi complex, and mitochondria. In addition, the number of pores per 10⯵m of karyotheca was another variable evaluated. The significance of the results between the two groups evaluated was analyzed by the Student's t test (pâ¯<â¯0.05). The cardiomyocytes obtained from animals of the old group showed decreased in sectional area and density of secretory granules of NP and lower relative volume of endoplasmic reticulum, Golgi complex, and mitochondria compared with the young rats. Moreover, the quantitative density of nuclear pores was significantly lower compared with the youngers. CONCLUSION: Aging causes hypotrophy of the cardiomyocytes of right atrium, similar to what occurs in ventricular cardiomyocytes.
Assuntos
Envelhecimento/fisiologia , Miócitos Cardíacos/metabolismo , Animais , Fator Natriurético Atrial/sangue , Pressão Sanguínea/fisiologia , Peso Corporal/fisiologia , Átrios do Coração/metabolismo , Ventrículos do Coração/metabolismo , Masculino , Peptídeo Natriurético Encefálico/sangue , Ratos , Ratos WistarRESUMO
TRPM8 is the main ion channel responsible for cold transduction in the somatosensory system. Nerve terminal availability of TRPM8 determines cold sensitivity, but how axonal secretory organelles control channel delivery remains poorly understood. Here we examine the distribution of TRPM8 and trafficking organelles in cold-sensitive peripheral axons and disrupt trafficking by targeting the ARF-GEF GBF1 pharmacologically or the small GTPase RAB6 by optogenetics. In axons of the sciatic nerve, inhibition of GBF1 interrupts TRPM8 trafficking and increases association with the trans-Golgi network, LAMP1, and Golgi satellites, which distribute profusely along the axonal shaft. Accordingly, both TRPM8-dependent ongoing activity and cold-evoked responses reversibly decline upon GBF1 inhibition in nerve endings of corneal cold thermoreceptors. Inhibition of RAB6, which also associates to Golgi satellites, decreases cold-induced responses in vivo. Our results support a non-conventional axonal trafficking mechanism controlling the availability of TRPM8 in axons and cold sensitivity in the peripheral nervous system.
Assuntos
Axônios/metabolismo , Temperatura Baixa , Organelas/metabolismo , Canais de Cátion TRPM/metabolismo , Animais , Axônios/efeitos dos fármacos , Complexo de Golgi/efeitos dos fármacos , Complexo de Golgi/metabolismo , Fatores de Troca do Nucleotídeo Guanina/metabolismo , Células HEK293 , Células HeLa , Humanos , Masculino , Mentol/farmacologia , Camundongos , Optogenética , Organelas/efeitos dos fármacos , Ligação Proteica/efeitos dos fármacos , Transporte Proteico/efeitos dos fármacos , Nervo Isquiático/efeitos dos fármacos , Nervo Isquiático/metabolismo , Termorreceptores/metabolismo , Proteínas rab de Ligação ao GTP/metabolismoRESUMO
The alterations that underlie the pathophysiology of schizophrenia (SCZ) include the dysregulation of structural and functional properties of neurons. Among these, the secretion of neurotransmitters and hormones, which plays a key role for neuronal communication and development, is altered. Neuronal precursors from the human olfactory epithelium have been recently characterized as a reliable model for studying the etiopathogenesis of neuropsychiatric diseases. Our previous work has shown that melatonin enhances the development of morphological and functional features of cloned olfactory neuronal precursors (ONPs) from a healthy subject. In this work we found that primary cultures of ONPs obtained from a schizophrenic patient display an increased potassium-evoked secretion, when compared with ONPs from an age- and gender-matched healthy control subject (HCS). Secretion was evaluated by FM1-43 fluorescence cumulative changes in response to depolarization. Interestingly, a 12 h-melatonin treatment modulated the abnormally increased secretion in SCZ ONPs and brought it to levels similar to those found in the HCS ONPs. Our results suggest that the actin cytoskeleton might be a target for melatonin effects, since it induces the thickening of actin microfilament bundles. Further research will address the mechanisms by which melatonin modulates neurochemical secretion from ONPs.
Assuntos
Melatonina/farmacologia , Células-Tronco Neurais/metabolismo , Mucosa Olfatória/patologia , Esquizofrenia/patologia , Citoesqueleto de Actina/metabolismo , Adulto , Cálcio/farmacologia , Humanos , Masculino , Células-Tronco Neurais/efeitos dos fármacos , Projetos Piloto , Potássio/farmacologia , Vesículas Secretórias/efeitos dos fármacos , Vesículas Secretórias/metabolismo , Sinapses/metabolismo , Proteína 1 Associada à Membrana da Vesícula/metabolismo , Proteína 2 Associada à Membrana da Vesícula/metabolismoRESUMO
ABSTRACT Introduction: Polypeptide hormones (natriuretic peptides, NPs) are secreted by the cardiac atria and play an important role in the regulation of blood pressure. Objective: To evaluate the effects of aerobic training on the secretory apparatus of NPs in cardiomyocytes of the right atrium. Methods: Nine-month-old mice were divided in two groups (n=10): control group (CG) and trained group (TG). The training protocol was performed on a motor treadmill for 8 weeks. Systolic blood pressure was measured at the beginning of the experiment (9 months of age) and at moment of the sacrifice (11 months of age). Electron micrographs were used to quantify the following variables: the quantitative density and area of NP granules, the relative volumes of the mitochondria, endoplasmic reticulum, and Golgi complex and the relative volume of euchromatin in the nucleus and the number of pores per 10 µm of the nuclear membrane. The results were compared by Student's t test (p< 0.05). Results: The cardiomyocytes obtained from TG mice showed increased density and sectional area of secretory granules of NP, higher relative volume of endoplasmic reticulum, mitochondria, and Golgi complex compared with the CG mice. Furthermore, the quantitative density of nuclear pores and the relative volume of euchromatin in the nucleus were significantly higher compared with the CG mice. Conclusion: Aerobic training caused hypertrophy of the secretory apparatus in the cardiomyocytes of right atrium, which could explain the intense synthesis of natriuretic peptides in trained mice with respect to the untrained mice.
RESUMO Introdução: Os hormônios polipeptídicos (peptídeos natriuréticos, PN) são secretados pelos átrios cardíacos e desempenham um papel importante na regulação da pressão arterial. Objetivo: Avaliar os efeitos do treinamento aeróbico sobre o aparelho secretor de PN nos cardiomiócitos do átrio direito. Métodos: Camundongos com nove meses de idade foram divididos em dois grupos (n = 10): grupo controle (GC) e grupo treinado (GT). O protocolo de treinamento foi realizado em esteira motorizada durante 8 semanas. A pressão sistólica dos animais foi medida no início do experimento (9 meses de idade) e no momento do sacrifício (11 meses). Foram usadas eletromicrografias para quantificar as seguintes variáveis densidade quantitativa e área dos grânulos de PN; volumes relativos (%) de mitocôndrias, retículo endoplasmático e aparelho de Golgi e o volume relativo de eucromatina no núcleo e o número de poros por 10 µm de membrana nuclear. Os resultados foram comparados pelo teste t de Student (p < 0,05). Resultados: Os cardiomiócitos obtidos dos camundongos GT apresentaram maior densidade e área seccional de grânulos secretórios de PN, aumento do volume relativo do retículo endoplasmático, das mitocôndrias e do complexo de Golgi, em comparação com os camundongos GC. Além disso, a densidade quantitativa dos poros nucleares e o volume relativo da eucromatina nuclear foram significantemente superiores em comparação com os camundongos GC. Conclusão: O treinamento aeróbico causou hipertrofia do aparelho secretor dos cardiomiócitos do átrio direito, o que poderia explicar a síntese intensa de peptídeos natriuréticos em camundongos treinados, quando comparados aos não treinados.
RESUMEN Introducción: Las hormonas polipeptídicas (péptidos natriuréticos, PN) son secretadas por las aurículas cardíacas y juegan un papel importante en la regulación de la presión arterial. Objetivo: Evaluar los efectos del entrenamiento aeróbico sobre el aparato secretor de PN en cardiomiocitos de la aurícula derecha. Métodos: Ratones de nueve meses de edad fueron divididos en dos grupos (n = 10): grupo control (GC) y grupo entrenado (GE). El protocolo de entrenamiento se realizó en cinta caminadora durante 8 semanas. La presión arterial sistólica se midió al inicio del experimento (9 meses de edad) y en el momento del sacrificio (11 meses de edad). Las electromicrografías se utilizaron para cuantificar las siguientes variables: la densidad cuantitativa y el área de gránulos de PN; los volúmenes relativos (%) de mitocondrias, del retículo endoplásmico y del aparato de Golgi y el volumen relativo de eucromatina en el núcleo y el número de poros por 10 µm de la membrana nuclear. Los resultados se compararon mediante la prueba t de Student (p < 0,05). Resultados: Los cardiomiocitos obtenidos de los ratones GE mostraron aumento de la densidad y del área seccional de gránulos secretorios de PN, aumento del volumen relativo de retículo endoplásmico, mitocondrias y aparato de Golgi en comparación con los ratones GC. Además, la densidad cuantitativa de los poros nucleares y el volumen relativo de la eucromatina nuclear fueron significativamente mayores en comparación con los ratones CG. Conclusión: El entrenamiento aeróbico causó hipertrofia del aparato secretor en los cardiomiocitos de la aurícula derecha, lo que podría explicar la intensa síntesis de péptidos natriuréticos en ratones entrenados con respecto a los ratones no entrenados.
RESUMO
A role of gelsolin in opening the way along the microvilli for secretory vesicles during microapocrine secretion is proposed here. Data obtained with different techniques showed that many digestive enzymes are released by microapocrine secretion in insects. Proteins that might be involved in the machinery of microapocrine secretion were selected from our transcriptomes and literature searches. The proteins were annexin, Complex actin-related proteins 2 and 3 (ARP 2/3) cofilin, fimbrin, gelsolin 1, gelsolin 2, moesin, myosin 1, myosin 6, protein disulphide isomerase 1 (PDI 1), PDI 2 and profilin. The cDNAs coding for annexin, fimbrin, gelsolin 1, myosin 1, PDI 1 and PDI 2 were cloned and their sequences deposited in GenBank. Only gelsolin 1 and myosin 1 are expressed exclusively in the midgut (semiquantitative reverse transcriptase PCR). As myosin 1 may have a structural role in microvilli, gelsolin 1 is the best guess to be involved in the secretory machinery. A truncated recombinant gelsolin 1 was used to generate antibodies with which it was shown labelling inside and around midgut cell microvilli shown in an electron microscope, reinforcing a microvillar role for gelsolin 1. Suppression of gelsolin 1 synthesis by RNA interference prevents secretory vesicles from advancing inside the microvilli, in agreement with its putative role in severing the actin filaments to free the way for the vesicles.
Assuntos
Gelsolina/genética , Proteínas de Insetos/genética , Spodoptera/genética , Animais , Clonagem Molecular , DNA Complementar/genética , DNA Complementar/metabolismo , Gelsolina/metabolismo , Proteínas de Insetos/metabolismo , Análise de Sequência de DNA , Spodoptera/metabolismoRESUMO
ABSTRACT Purpose: In the lacrimal gland (LG) acinar cells, signaling regulates the release of secretory vesicles through specific Rab and SNARE exocytotic proteins. In diabetes mellitus (DM), the LGs are dysfunctional. The aim of this work was to determine if secretory apparatus changes were associated with any effects on the secretory vesicles (SV) in diabetic rats as well as the expression levels of constituent Rab and members of the SNARE family, and if insulin supplementation reversed those changes. Methods: DM was induced in male Wistar rats with an intravenous dose of streptozotocin (60 mg/kg). One of the two diabetic groups was then treated every other day with insulin (1 IU). A third control group was injected with vehicle. After 10 weeks, Western blotting and RT-PCR were used to compared the Rab and SNARE secretory factor levels in the LGs. Transmission electron microscopy evaluated acinar cell SV density and integrity. Results: In the diabetes mellitus group, there were fewer and enlarged SV. The Rab 27b, Rab 3d, and syntaxin-1 protein expression declined in the rats with diabetes mellitus. Insulin treatment restored the SV density and the Rab 27b and syntaxin expression to their control protein levels, whereas the Vamp 2 mRNA expression increased above the control levels. Conclusions: Diabetes mellitus LG changes were associated with the declines in protein expression levels that were involved in supporting exocytosis and vesicular formation. They were partially reversed by insulin replacement therapy. These findings may help to improve therapeutic management of dry eye in diabetes mellitus. .
RESUMO Objetivo: Células acinares da glândula lacrimal (GL) sinalizam a regulação da liberação através de vesículas secretórias específicas Rab proteínas exocitóticas SNARE. No diabetes mellitus (DM), as glândulas lacrimais são disfuncionais. O objetivo deste trabalho foi determinar se em ratos diabéticos, alterações dos aparatos secretórios estão associados a efeitos sobre vesículas secretoras (VS) e sobre os níveis de expressão do constituinte Rab, bem como membros da família SNARE, e se a suplementação de insulina reverte as alterações. Métodos: DM foi induzido em ratos Wistar machos com uma dose intravenosa de estreptozotocina (60 mg/kg). Um dos dois grupos diabéticos foi então tratado a cada dois dias com insulina (1 UI). Um terceiro grupo controle foi injetado com o veículo. Após 10 semanas, western blot e RT-PCR comparou níveis de fatores secretórios de Rab e SNARE na glândula lacrimal. Microscopia eletrônica de transmissão (MET) avaliaram a densidade e integridade de VS de célula acinar. Resultados: No grupo diabetes mellitus , houve poucas e alargadas VS. Rab27b, Rab 3d e Sintaxina-1 diminuiu a expressão da proteína em ratos com Diabetes Mellitus. O tratamento com insulina restaurou a densidade das VS e expressão de Rab 27b e Sintaxina para seus níveis de proteína controle, enquanto a expressão de Vamp 2 RNAm aumentou em relação aos controles. Conclusões: Alterações na glândula lacrimal de diabetes mellitus estão associadas a reduções nos níveis de expressão de proteínas envolvidas no apoio a exocitose e formação vesicular. Eles são, em parte, revertida por terapia de reposição de insulina. Estes resultados podem ajudar a melhorar a conduta terapêutica do olho seco no diabetes mellitus. .