Anti-TGFß (Transforming Growth Factor ß) Therapy With Betaglycan-Derived P144 Peptide Gene Delivery Prevents the Formation of Aortic Aneurysm in a Mouse Model of Marfan Syndrome.

Objective: We investigated the effect of a potent TGFß (transforming growth factor ß) inhibitor peptide (P144) from the betaglycan/TGFß receptor III on aortic aneurysm development in a Marfan syndrome mouse model. Approach and Results: We used a chimeric gene encoding the P144 peptide linked to apolipoprotein A-I via a flexible linker expressed by a hepatotropic adeno-associated vector. Two experimental approaches were performed: (1) a preventive treatment where the vector was injected before the onset of the aortic aneurysm (aged 4 weeks) and followed-up for 4 and 20 weeks and (2) a palliative treatment where the vector was injected once the aneurysm was formed (8 weeks old) and followed-up for 16 weeks. We evaluated the aortic root diameter by echocardiography, the aortic wall architecture and TGFß signaling downstream effector expression of pSMAD2 and pERK1/2 by immunohistomorphometry, and Tgfß1 and Tgfß2 mRNA expression levels by real-time polymerase chain reaction. Marfan syndrome mice subjected to the preventive approach showed no aortic dilation in contrast to untreated Marfan syndrome mice, which at the same end point age already presented the aneurysm. In contrast, the palliative treatment with P144 did not halt aneurysm progression. In all cases, P144 improved elastic fiber morphology and normalized pERK1/2-mediated TGFß signaling. Unlike the palliative treatment, the preventive treatment reduced Tgfß1 and Tgfß2 mRNA levels. Conclusions: P144 prevents the onset of aortic aneurysm but not its progression. Results indicate the importance of reducing the excess of active TGFß signaling during the early stages of aortic disease progression.

Morfo-anatomía del ciclo de vida del helecho Pteridium aquilinum (Dennstaedtiaceae) en cultivo in vitro

Introducción: Pteridium aquilinum es un helecho heliófilo ampliamente distribuido en México. Es una especie pionera que usualmente se encuentra en hábitats alterados y tiene gran relevancia ecológica por sus propiedades alelopáticas, su resistencia al fuego y a condiciones de sequía. Objetivo: Realizar una descripción integral de la forma y ornamentación de las esporas de P. aquilinum, así como de la morfogénesis del gametofito, incluyendo el tipo de germinación y el desarrollo protálico (resaltando su morfología). Además, describir la anatomía del esporofito joven desarrollado en condiciones in vitro. Metodología: Se utilizó microscopía electrónica de barrido y técnica histológica de parafina para la descripción de las fases del gametofito y esporofito. Resultados: Las esporas son globulares y el trilete tiene ornamentación granulada, mientras que su germinación fue de tipo Vittaria y el desarrollo protálico correspondió al tipo Adiantum. Los anteridios se observaron 13 días después de la siembra, mientras que los arquegonios surgieron al día 17. La primera hoja del esporofito apareció entre los días 60 y 70. Al cuarto mes, la fase esporofítica desarrollada in vitro mostró la anatomía típica de la especie a esta edad, dado que no presentó vitrificación. El análisis histológico del rizoma, la base del peciolo, el raquis de primer orden y la lámina mostraron los sistemas de tres tejidos bien diferenciados. Las modificaciones anatómicas observadas in vitro, como una dictiostela monocíclica y sólo una banda de esclerénquima en el rizoma, podrían atribuirse a la edad de los individuos. Por otra parte, los estomas están presentes en la superficie adaxial de la lámina, que corresponde al tipo anomocítico. Aunque estos estomas se formaron en condiciones in vitro, es importante resaltar que son completamente funcionales. Conclusiones: Nuestro trabajo describe por primera vez la morfo-anatomía de las fases gametofítica y esporofítica del ciclo de vida de P. aquilinum en condiciones in vitro. Nuestros resultados posiblemente permitan la exploración con mayor profundidad de las propiedades biológicas, fisiológicas y ecológicas de la especie.

Introduction: Pteridium aquilinum is a heliophilous fern widely distributed in Mexico. It is a pioneer species usually found within disturbed habitats with high ecological relevance because of its allelopathic properties, its resistance to fire and drought conditions. Objective: Provide an integrative description regarding P. aquilinum spores shape and ornamentation, and also on gametophyte morphogenesis, including the type of germination and the prothallic development (highlighting its morphology). Furthermore, the anatomy of young sporophyte grown under in vitro conditions was described. Methods: We used scanning electron microscopy and histological paraffin technique to describe the gametophytic and sporophytic phases. Results: The evaluation of the spores showed the presence of globular morphology and triletes with granulated ornamentation; while their germination was Vittaria-type, the prothallic development corresponded to the Adiantum-type. The antheridia were observed 13 days following to the sowing, whereas archegonia arose at day 17. The first leaf of the sporophyte appeared between days 60 and 70. At fourth month, the in vitro grown sporophyte showed the typical anatomy of the individuals of the species at this age, since it did not exhibit vitrification. The histological analysis of rhizome, the petiole base, first order rachis and lamina showed the three tissue systems well differentiated. The anatomical modifications observed in vitro, such as a non-polycyclic dictyostele and just one band sclerenchyma in the rhizome, may be attributed to the individuals age. Moreover, the stomata are present on the adaxial surface of lamina, corresponding to the anomocytic type. Although these stomata were developed under in vitro conditions, it is important to highlight that they are completely functional. Conclusions: Our work describes for the first time the morpho-anatomy of both the gametophytic and the sporophytic phases in the life cycle of P. aquilinum under in vitro conditions. Our results indicate that this method will allow deeper exploration of biological, physiological and ecological properties of the species.

NaStEP: a proteinase inhibitor essential to self-incompatibility and a positive regulator of HT-B stability in Nicotiana alata pollen tubes.

In Solanaceae, the self-incompatibility S-RNase and S-locus F-box interactions define self-pollen recognition and rejection in an S-specific manner. This interaction triggers a cascade of events involving other gene products unlinked to the S-locus that are crucial to the self-incompatibility response. To date, two essential pistil-modifier genes, 120K and High Top-Band (HT-B), have been identified in Nicotiana species. However, biochemistry and genetics indicate that additional modifier genes are required. We recently reported a Kunitz-type proteinase inhibitor, named NaStEP (for Nicotiana alata Stigma-Expressed Protein), that is highly expressed in the stigmas of self-incompatible Nicotiana species. Here, we report the proteinase inhibitor activity of NaStEP. NaStEP is taken up by both compatible and incompatible pollen tubes, but its suppression in Nicotiana spp. transgenic plants disrupts S-specific pollen rejection; therefore, NaStEP is a novel pistil-modifier gene. Furthermore, HT-B levels within the pollen tubes are reduced when NaStEP-suppressed pistils are pollinated with either compatible or incompatible pollen. In wild-type self-incompatible N. alata, in contrast, HT-B degradation occurs preferentially in compatible pollinations. Taken together, these data show that the presence of NaStEP is required for the stability of HT-B inside pollen tubes during the rejection response, but the underlying mechanism is currently unknown.

Pollination in Nicotiana alata stimulates synthesis and transfer to the stigmatic surface of NaStEP, a vacuolar Kunitz proteinase inhibitor homologue.

After landing on a wet stigma, pollen grains hydrate and germination generally occurs. However, there is no certainty of the pollen tube growth through the style to reach the ovary. The pistil is a gatekeeper that evolved in many species to recognize and reject the self-pollen, avoiding endogamy and encouraging cross-pollination. However, recognition is a complex process, and specific factors are needed. Here the isolation and characterization of a stigma-specific protein from N. alata, NaStEP (N. alata Stigma Expressed Protein), that is homologous to Kunitz-type proteinase inhibitors, are reported. Activity gel assays showed that NaStEP is not a functional serine proteinase inhibitor. Immunohistochemical and protein blot analyses revealed that NaStEP is detectable in stigmas of self-incompatible (SI) species N. alata, N. forgetiana, and N. bonariensis, but not in self-compatible (SC) species N. tabacum, N. plumbaginifolia, N. benthamiana, N. longiflora, and N. glauca. NaStEP contains the vacuolar targeting sequence NPIVL, and immunocytochemistry experiments showed vacuolar localization in unpollinated stigmas. After self-pollination or pollination with pollen from the SC species N. tabacum or N. plumbaginifolia, NaStEP was also found in the stigmatic exudate. The synthesis and presence in the stigmatic exudate of this protein was strongly induced in N. alata following incompatible pollination with N. tabacum pollen. The transfer of NaStEP to the stigmatic exudate was accompanied by perforation of the stigmatic cell wall, which appeared to release the vacuolar contents to the apoplastic space. The increase in NaStEP synthesis after pollination and its presence in the stigmatic exudates suggest that this protein may play a role in the early pollen-stigma interactions that regulate pollen tube growth in Nicotiana.