Estrogen-receptor-related receptor gamma, ERRγ, is highly expressed in cartilage and upregulates the chondrogenic transcription factor, Sox9, in a chondrocytic cell line. To assess the effect of increasing ERRγ activity on cartilage in vivo, we generated transgenic animals driving ERRγ expression with a chondrocyte-specific promoter. I verified that one transgenic line exhibited 26% increased ERRγ protein at E14.5. No major morphological defects were seen at this stage, but I observed significant reduction in the size of the appendicular skeleton in P7 mice, such that all elements of the appendicular skeleton were significantly reduced by 4 – 10%. I continued the phenotype analysis at the histological level and found that the P7 animals displayed significantly reduced growth plate height, caused by deficiencies in the size of the proliferative and hypertrophic zones of the growth plate. This suggests a previously unknown role for ERRγ in regulating endochondral ossification in growth plate chondrocytes.

The vertebrate Dlx gene family consists of multiple convergently transcribed bigene clusters and encodes a group of homeodomain-containing transcription factors crucial for the development of forebrain, branchial arches, sensory organs and limbs. At least four cis-regulatory elements (CREs) are responsible for Dlx expression in the forebrain: URE2 and I12b in the Dlx1/Dlx2 (zebrafish dlx1a/dlx2a) locus, and, I56i and I56ii in the Dlx5/Dlx6 (zebrafish dlx5a/dlx6a) locus. Here, we first show that unlike the other three enhancers, mouse I56ii CRE targets a group of GABAergic projection neurons expressing striatal markers Meis2 and Islet1. Meis2 and Islet1 proteins can activate reporter gene transcription via the I56ii CRE, suggesting that they may be potential upstream regulators of Dlx genes in vivo. To determine whether there exists a dlx-mediated regulatory pathway during zebrafish GABAergic neuron formation, we establish two independent lines of transgenic fish in which the GFP reporter gene is controlled by a 1.4kb dlx5a/dlx6a intergenic sequence (encompassing zebrafish I56i and I56ii) and a 1.1kb fragment containing only I56i CRE, respectively. Our observations reveal that dlx5a/dlx6a regulatory elements exhibit a fairly specific activity in the zebrafish forebrain and may be essential for GABAergic neuron generation, while I56i and I56ii are likely to play distinct roles in modulating this process in different subpopulations of cells. Disruption of dlx1a/dlx2a or dlx5a/dlx6a function leads to a marked decrease of enhancer activity in the diencephalon and midbrain as well as a comparatively lesser extent of reduction in the telencephalon. In order to define the specific contribution of various individual CREs to overall Dlx regulation, we also generate a mutant mouse model in which I12b CRE is selectively deleted. Despite that mice homozygous for I12b loss develop normally and harbor no overt morphological defects in the forebrain, targeted deletion of this enhancer results in a significant reduction of Dlx1/Dlx2 transcript levels and seemingly perturbs cell proliferation in the subpallial telencephalon, particularly in the ventricular and subventricular zones of ganglionic eminences. Taken together, these data illustrate a complex and dynamic Dlx regulation in the early developing forebrain through the implications of multiple Dlx CREs with overlapping and diverse functions.

The vertebrate Dlx gene family consists of multiple convergently transcribed bigene clusters and encodes a group of homeodomain-containing transcription factors crucial for the development of forebrain, branchial arches, sensory organs and limbs. At least four cis-regulatory elements (CREs) are responsible for Dlx expression in the forebrain: URE2 and I12b in the Dlx1/Dlx2 (zebrafish dlx1a/dlx2a) locus, and, I56i and I56ii in the Dlx5/Dlx6 (zebrafish dlx5a/dlx6a) locus. Here, we first show that unlike the other three enhancers, mouse I56ii CRE targets a group of GABAergic projection neurons expressing striatal markers Meis2 and Islet1. Meis2 and Islet1 proteins can activate reporter gene transcription via the I56ii CRE, suggesting that they may be potential upstream regulators of Dlx genes in vivo. To determine whether there exists a dlx-mediated regulatory pathway during zebrafish GABAergic neuron formation, we establish two independent lines of transgenic fish in which the GFP reporter gene is controlled by a 1.4kb dlx5a/dlx6a intergenic sequence (encompassing zebrafish I56i and I56ii) and a 1.1kb fragment containing only I56i CRE, respectively. Our observations reveal that dlx5a/dlx6a regulatory elements exhibit a fairly specific activity in the zebrafish forebrain and may be essential for GABAergic neuron generation, while I56i and I56ii are likely to play distinct roles in modulating this process in different subpopulations of cells. Disruption of dlx1a/dlx2a or dlx5a/dlx6a function leads to a marked decrease of enhancer activity in the diencephalon and midbrain as well as a comparatively lesser extent of reduction in the telencephalon. In order to define the specific contribution of various individual CREs to overall Dlx regulation, we also generate a mutant mouse model in which I12b CRE is selectively deleted. Despite that mice homozygous for I12b loss develop normally and harbor no overt morphological defects in the forebrain, targeted deletion of this enhancer results in a significant reduction of Dlx1/Dlx2 transcript levels and seemingly perturbs cell proliferation in the subpallial telencephalon, particularly in the ventricular and subventricular zones of ganglionic eminences. Taken together, these data illustrate a complex and dynamic Dlx regulation in the early developing forebrain through the implications of multiple Dlx CREs with overlapping and diverse functions.

Transgenesis of silkworms has great potential for the development of silk with new properties as well as for the preparation of recombinant proteins for the use in biomedicine. Zabelina et al. (2015a) showed that transgenesis of parthenogenetic silkworms facilitates the selection and maintenance of transgenic homozygotes with stabile transgene insertions. However, the efficiency of transgenesis was less than 2 % compared to 60 % in the standard, non-parthenogenetic silkworms. The purpose of the present research was to explore the cause of this difference. Since transgenesis is normally performed at 25 °C but in the parthenogenetic silkworms at 15 °C (3 days incubation at this temperature is part of the protocol for the induction of parthenogenetic development), we assumed that the eggs incubated at 15 °C might have been injected with the DNA construct at unsuitable time. The work was therefore focused on the rate of embryogenesis at 15 °C in the eggs treated in different ways. Intensive cleavage of the control eggs (strain K23) was observed at 12 h after oviposition at 25 °C and between 24 and 36 h at 15 °C. The transgenesis of parthenogenetic silkworms is also complicated by the embryonic diapause. In the current work, diapause was suppressed by implanting PK1 ovaries into the non-parthenogenetic male hosts K23. Parthenogenetic development was activated by the heat shock in the chorionated eggs dissected from the implants. No cleavage was detected at 12 h after the acti-vation and nearly complete blastoderm was found at 48 h. In respect to the course of cleavage at 15 °C, transgene injection 24 h after the activating heat shock can be recommended. The eggs from endogenous ovaries of the K23 females, which also contained the implants of the PK1 ovaries, acquired partial capacity of parthenogenesis. Low rate of embryogenesis was also found in the transgenic clone VTG1. Current results suggest that more research is needed to understand and possibly explore differences in the rate of silkworms exposed to different treatments.

Submitted by Bruna Rodrigues (bruna92rodrigues@yahoo.com.br) on 2016-10-20T12:18:16Z No. of bitstreams: 1 DissVCSS.pdf: 2091589 bytes, checksum: bf27e402ae83e3965ce2a5d5772a3fb7 (MD5) / Approved for entry into archive by Marina Freitas (marinapf@ufscar.br) on 2016-11-08T18:39:56Z (GMT) No. of bitstreams: 1 DissVCSS.pdf: 2091589 bytes, checksum: bf27e402ae83e3965ce2a5d5772a3fb7 (MD5) / Approved for entry into archive by Marina Freitas (marinapf@ufscar.br) on 2016-11-08T18:40:02Z (GMT) No. of bitstreams: 1 DissVCSS.pdf: 2091589 bytes, checksum: bf27e402ae83e3965ce2a5d5772a3fb7 (MD5) / Made available in DSpace on 2016-11-08T18:40:07Z (GMT). No. of bitstreams: 1 DissVCSS.pdf: 2091589 bytes, checksum: bf27e402ae83e3965ce2a5d5772a3fb7 (MD5) Previous issue date: 2015-09-27 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / Assuming that the use of (GMOs) in agriculture is controversial, this paper discusses one of the strongest reasons in favor of such technology: as a mean to combat hunger. To assess this joint between transgenesis and combat hunger, the RENORBIO’s researchers network (“Rede de Biotecnologia do Nordeste” - Biotechnology Network in the Northeast) has been selected to this study for stating “the use of bioscience advances to reduce hunger "as one of its interests. The present work presents a sociological point of view on the advancement of technology in agriculture, seeking to understand the progression of GM farming in crops from some reading about modern techniques. Then the question of risk and how it is produced nowadays is discussed, and, after that, the Agroecology is presented as an alternative to transgenic agricultural management. Only then, the fight against hunger is questioned, as something controversial, whose solution options depend on different worldviews. Finally, are presented some major explanations of RENORBIO, its allies, its articulations and their researches on transgenesis. / Partindo do princípio de que o uso de transgênicos na agricultura é algo controverso, este trabalho visa discutir uma das justificativas mais fortes em favor desse tipo de tecnologia: a transgênese como uma tecnologia necessária para o combate à precarização alimentar. Para avaliar como anda essa articulação (entre transgênicos e combate à fome) foi estudada a rede de pesquisadores RENORBIO (Rede de Biotecnologia do Nordeste), pois esta estabelece “a utilização dos avanços da biociência para reduzir a fome” como um dos seus interesses. Com esse fim, o presente trabalho faz uma leitura sociológica do avanço da tecnologia na agricultura, buscando entender a progressão do cultivo de transgênicos nas lavouras a partir de algumas leituras sobre a técnica moderna. Em seguida, a questão do risco e de como ele é produzido na contemporaneidade é discutida, e, então, a Agroecologia é apresentada como outra forma de manejo agrícola alternativa aos transgênicos. Só então, o combate a fome é problematizado, como algo controverso, cujo as vias de solução dependem de visões de mundo diferenciadas. Por fim, são feitas maiores explanações sobre a RENORBIO, seus aliados, sua forma de articulação e suas pesquisas em transgênese.

A espermatogênese em mamíferos é um processo sustentado pela auto-renovação e diferenciação de células-tronco espermatogoniais (SSCs). O estudo destas células oferece um excelente modelo para o melhor entendimento da biologia das células-tronco adultas e dos mecanismos que controlam as funções das SSCs. Além do potencial biomédico para estudos sobre infertilidade em diferentes espécies, as SSC possuem uma aplicação promissora na biotecnologia para a produção de animais transgênicos. Assim, o objetivo deste trabalho foi responder à pergunta: "SSCs bovinas LacZ+ podem integrar-se aos túbulos seminíferos de bezerros pré-púberes da raça Nelore após transplante autólogo?" Para isso, bezerros Nelore de 5 meses de idade (n=16) foram submetidos a uma orquiectomia unilateral para o isolamento de células espermatogoniais por digestão enzimática. Após o plaqueamento diferencial, as células foram transduzidas com um vetor lentiviral contendo a sequencia do gene marcador LacZ. Para isso, os animais foram aleatoriamente alocados em um dos quatro grupos experimentais: LacZ+/PKH26+, LacZ+/PKH26-, LacZ-/PKH26+, LacZ-/PKH26-. Após 60 h do início do cultivo in vitro, as células espermatogoniais foram transplantadas autologamente para o mediastino do testículo remanescente por injeção guiada por ultrassonografia. O testículo transplantado foi removido cirurgicamente após 45 dias e amostras de tecido foram submetidas a reação com x-gal para verificação da integração de células espermatogoniais transgênicas aos túbulos seminíferos. Células espermatogoniais foram isoladas e cultivadas in vitro com sucesso. Contudo, não foi possível obter uma população pura de SSCs por plaqueamento diferencial. Embora tenha sido eleito o transplante de células espermatogoniais e não de SSCs somente, sabe-se que também foram transplantadas SSCs, pois a caracterização das células isoladas demonstrou a expressão dos marcadores de SSCs ITGA6, GFRa-1, PGP 9.5 e afinidade pela lectina DBA. Crioseções de amostras de tecido testicular coradas com x-gal permitiram a observação de células transgênicas em 8 de 8 animais que receberam células LacZ+. Contudo, todas as células transgênicas observadas estavam situadas no interstício. Concluindo, não foi possível observar a integração das células transgênicas transplantadas aos túbulos seminíferos do testículo receptor após 45 dias do transplante autólogo utilizando a técnica de injeção intratesticular de células espermatogoniais LacZ+ no mediastino de bezerros pré-púberes da raça Nelore. / Mammalian spermatogenesis is sustained by self renewal and differentiation of spermatogonial stem cells (SSCs). The study of these cells provides a model to better understand adult stem cell biology and the mechanisms that control SSC functions. Besides the biomedical potential to perform studies of infertility in many species, SSCs hold a promising biotechnological application at animal transgenesis. In this manner, the goal of this study was to answer the question: "Can LacZ+ bovine SSCs be integrated into seminiferous tubule of prepubertal Nelore bulls subjected to autologous transplantation?" Hence, 5 months old bulls (n=16) were hemicastrated and spermatogonial cells were isolated by a two step enzymatic digestion procedure. After differential plating, cells were transduced with a lentivirus vector carrying the LacZ reporter gene sequence. Animals were randomly allocated in four experimental groups: LacZ+/PKH26+, LacZ+/PKH26-, LacZ-/PKH26+, LacZ-/PKH26-. After 60 h of the onset of in vitro culture, spermatogonial cells were autologously transplanted to the remaining testes by an ultrasound guided needle injection at the testis mediastinum. The transplanted testes were surgically removed after 45 days and testicular tissue samples were subjected to x-gal staining to assess the integration of transgenic spermatogonial cells to seminiferous tubule. Spermatogonial cells were successfully isolated and in vitro cultured. However, it was not possible to obtain a SSC enriched population of cells by differential plating. Although it was decided by the transplant of spermatogonial cells instead of pure SSCs only, it was detected the expression of SSC marker genes ITGA6, PGP9.5, GFR-1 and the affinity for DBA by the isolated cells. Cryosections of x-gal stained testicular tissue samples allowed the observation of transgenic cells in 8 out of 8 animals that received LacZ+ cells. However, all transgenic cells observed were located at the interstitial space. In conclusion, it was not possible to observe the integration of the transplanted transgenic cells into seminiferous tubule of prepubertal Nelore bulls subjected to autologous transplantation using an ultrasound guided needle injection at the testis mediastinum, after 45 days of transplant.

The vertebrate Dlx gene family consists of multiple convergently transcribed bigene clusters and encodes a group of homeodomain-containing transcription factors crucial for the development of forebrain, branchial arches, sensory organs and limbs. At least four cis-regulatory elements (CREs) are responsible for Dlx expression in the forebrain: URE2 and I12b in the Dlx1/Dlx2 (zebrafish dlx1a/dlx2a) locus, and, I56i and I56ii in the Dlx5/Dlx6 (zebrafish dlx5a/dlx6a) locus. Here, we first show that unlike the other three enhancers, mouse I56ii CRE targets a group of GABAergic projection neurons expressing striatal markers Meis2 and Islet1. Meis2 and Islet1 proteins can activate reporter gene transcription via the I56ii CRE, suggesting that they may be potential upstream regulators of Dlx genes in vivo. To determine whether there exists a dlx-mediated regulatory pathway during zebrafish GABAergic neuron formation, we establish two independent lines of transgenic fish in which the GFP reporter gene is controlled by a 1.4kb dlx5a/dlx6a intergenic sequence (encompassing zebrafish I56i and I56ii) and a 1.1kb fragment containing only I56i CRE, respectively. Our observations reveal that dlx5a/dlx6a regulatory elements exhibit a fairly specific activity in the zebrafish forebrain and may be essential for GABAergic neuron generation, while I56i and I56ii are likely to play distinct roles in modulating this process in different subpopulations of cells. Disruption of dlx1a/dlx2a or dlx5a/dlx6a function leads to a marked decrease of enhancer activity in the diencephalon and midbrain as well as a comparatively lesser extent of reduction in the telencephalon. In order to define the specific contribution of various individual CREs to overall Dlx regulation, we also generate a mutant mouse model in which I12b CRE is selectively deleted. Despite that mice homozygous for I12b loss develop normally and harbor no overt morphological defects in the forebrain, targeted deletion of this enhancer results in a significant reduction of Dlx1/Dlx2 transcript levels and seemingly perturbs cell proliferation in the subpallial telencephalon, particularly in the ventricular and subventricular zones of ganglionic eminences. Taken together, these data illustrate a complex and dynamic Dlx regulation in the early developing forebrain through the implications of multiple Dlx CREs with overlapping and diverse functions.

The objective of part one of this study was to determine if the presence of porcine growth hormone (pGH) during oocycte in vitro maturation (IVM) affected subsequent embryo development. Pig cumulus-oocyte complexes (COC) (n=987) were aspirated from slaughterhouse derived ovaries and cultured in BSA-free NCSU 23 medium containing porcine follicular fluid (10% v/v), cysteine (0.1 mg/ml) and hormonal supplements (eCG and hCG, 10 IU/ml each), 10 ng/ml EGF, and with or without pGH (100 ng/ml) for 22 h. The COC were then cultured in the same medium with or without 100 ng/ml pGH, but without hormonal supplements for an additional 22 h. After the completion of maturation culture, cumulus cells were removed and oocytes were co-incubated with frozen-thawed spermatozoa for 8 h. Putative embryos were transferred to NCSU 23 containing 0.4% BSA and cultured for 144 h. Embryo development was assessed on d 6 of culture. The treatment groups were as follows: treatment 1 = control group cultured in IVM medium alone; treatment 2 = 100 ng/ml pGH present of the first 22 h of maturation culture and absent for the second 22 h of maturation culture; treatment 3 = 100 ng/ml pGH absent for the first 22 h of maturation culture, but present for the second 22 h of maturation culture; and treatment 4 = 100 ng/ml pGH present throughout the entire IVM period. Embryos were visually scored for developmental stage at 144 h following fertilization. Each oocyte in the study received a developmental score, based on a scale of 1 = uncleaved, 2 = 2-cell embryo, 3 = 4- to 8-cell embryo, 4 = 9- to 16-cell embryo, 5 = morula, and 6 = blastocyst. The addition of pGH did not affect porcine embryo development as compared to the control (1.57 ± .08, 1.67 ± .08, 1.47 ± .08, and 1.60 ± .08, respectively; P > .10). Replicates within the study differed significantly from each other (P < .01) primarily because the development in replicate 6 was greater than for all others. There was a significant treatment by replicate interaction (P < .05); pGH added during the first 22 h of IVM and pGH added during the second 22 h of IVM in replicate 6 resulted in higher development scores than for controls and continuous pGH addition. However, in replicate 2, continuous pGH resulted in the greatest development. These results suggest that pGH may exert a stimulatory effect on embryo development when present in the IVM media; however, further studies using pGH in IVM culture are necessary. The objectives of the second part of the study were to examine aspects of intracytoplasmic sperm injection (ICSI) using membrane-disrupted spermatozoa, in vitro fertilization (IVF), and sperm-mediated gene transfer in the pig. Porcine oocytes were shipped overnight in maturation media at 39°C in a portable incubator. After 22 h of maturation culture, oocytes were washed in maturation medium without gonadotropins and cultured for an additional 22 h. Cumulus cells were removed and oocytes were divided into four treatment groups: treatment 1 = ICSI using membrane-damaged spermatozoa coincubated with linear green fluorescent protein (GFP) DNA; treatment 2 = ICSI using membrane damaged spermatozoa; treatment 3 = IVF with frozen-thawed spermatozoa coincubated with linear GFP DNA prior to IVF; treatment 4 = IVF with frozen-thawed spermatozoa with no DNA coincubation. Embryos were scored for developmental stage at 144 h following fertilization. Each oocyte in the study received a developmental score, based on a scale of 1 = uncleaved, 2 = 2-cell embryo, 3 = 4-cell embryo, 4 = 5- to 8-cell embryo, 5 = 9- to 16-cell embryo, 6 = morula, and 7 = blastocyst. Although no overall difference in development score was observed following the four different treatments, a treatment difference among cleaved oocytes was observed when comparing only the two ICSI treatments (P < .05); development scores were greater in the ICSI treatment in which sperm were not coincubated with linear GFP DNA prior to injection than when the coincubation was performed (3.76 ± .21 vs. 3.13 ± .17, respectively). No differences in development score were observed in the two IVF treatments. The percentage of embryos expressing the GFP transgene on d 6 of culture following fertilization was 7.3% in the ICSI+GFP group and 0% in all other treatment groups. Thus, sperm-mediated gene transfer using ICSI in the pig has been demonstrated, although success rates were low. / Master of Science

La ligne latérale postérieure embryonnaire du poisson-zèbre est composée d'un ensemble d'organes sensoriels, appelés neuromastes, qui permet au poisson de détecter les mouvements de l'eau. Le primordium qui génère la ligne latérale postérieure embryonnaire migre de la tête vers l'extrémité de la queue le long d'une piste de cellules sécrétrices de SDF-1, et dépose des groupes de cellules précurseurs des neuromastes. Cette migration dépend de la présence de CXCR4, le récepteur de SDF-1, dans la région en tête du primordium et de la présence du second récepteur de SDF-1, CXCR7, dans la région en queue du primordium. L'objectif de ma thèse est d'identifier des régulateurs de l'expression de cxcr4b au sein du primordium. Nous avons montré que l'inactivation du récepteur des strogènes ESR1 induit l'expression ectopique de cxcr4b dans les cellules de queue du primordium alors que sa surexpression induit une réduction du domaine d'expression de cxcr4b, suggérant que ESR1 agit comme un répresseur de cxcr4b. Cette découverte expliquerait pourquoi les strogènes diminuent la capacité métastatique des cellules du cancer du sein strogéno-dépendants. L'inactivation de ESR1 conduit aussi à l'extinction de l'expression de cxcr7b dans les cellules de queue du primordium, cet effet étant toutefois indirect et induit par la signalisation ectopique SDF-1/CXCR4 dans ces cellules. L'inactivation et la surexpression de ESR1 provoquent toutes deux une migration défectueuse du primordium, confirmant l'importance de ce récepteur dans le contrôle de la migration dépendante de SDF-1. Nous avons aussi montré qu'un effecteur majeur de la signalisation Wnt canonique, LEF-1, contribue au contrôle de l'expression de cxcr4b et de cxcr7b dans les cellules en tête du primordium. Nous montrons que la prolifération cellulaire, qui assure une taille constante du primordium en dépit des dépositions successives de cellules, est réduite en absence de LEF-1, et que cela conduit à une ligne latérale postérieure incomplète. / The zebrafish embryonic posterior lateral line is componed by a set sense organs, called neuromasts, allowing the fish to detect the water movements. The primordium that generates the embryonic posterior lateral line of zebrafish migrates from the head to the tip of the tail along a trail of SDF-1-producing cells, and deposits cell groups that will become the neuromasts. This migration critically depends on the presence of the SDF-1 receptor CXCR4 in the leading region of the primordium and on the presence of a second SDF1 receptor, CXCR7, in the trailing region of the primordium. The aim of my thesis is to identify regulators of the cxcr4b expression within the primordium. Here we show that inactivation of the estrogen receptor ESR1 results in ectopic expression of cxcr4b throughout the primordium, whereas ESR1 overexpression results in a reciprocal reduction in the domain of cxcr4b expression, suggesting that ESR1 acts as a repressor of cxcr4b. This finding could explain why estrogens significantly decrease the metastatic ability of ESR-positive breast cancer cells. ESR1 inactivation alsoleads to extinction of cxcr7b expression in the trailing cells of the migrating primordium; this effect is indirect, however, and due to the down-regulation of cxcr7b by ectopic SDF-1/CXCR4 signaling in the trailing region. Both ESR1 inactivation and overexpression result in aborted migration, confirming the importance of this receptor in the control of SDF-1-dependent migration. We also showed that a major effector of the canonical Wnt signaling, LEF-1, contributes to the control of both cxcr4b and cxcr7b expression in the leading cells of the primordium. We show that cell proliferation, which ensures constant primordium size in spite of sucessive rounds of cell deposition, is reduced upon lef1 inactivation, leading in a truncated posterior lateral line.

Ao longo da vida reprodutiva dos machos adultos, espermatozoides são formados pelas células-tronco espermatogoniais (SSCs, do inglês spermatogonial stem cells) por um processo conhecido como espermatogênese. O cultivo in vitro de SSCs abriu novas possibilidades para a transgenia, no entanto os protocolos requerem a adição de fatores de crescimento, o que encarece a manutenção dessas células por um tempo prolongado, fazendo da criopreservação de SSCs uma alternativa para esse problema. O fenótipo molecular de células-tronco espermatogoniais tem sido objeto de estudo nas últimas décadas. Uma das moléculas mais estudadas como marcador na caracterização de espermatogônias é a alfa-6 integrina. Baseado nestas informações, a seguinte hipótese foi proposta: SSCs que apresentam maior expressão de alfa-6 integrina são mais eficientes para modificações genéticas e colonização de túbulos seminíferos. Para testar essa hipótese, as SSCs murinas foram dissociadas de testículos de camundongos com 8 a 11 dias de idade. Essas células foram cultivadas in vitro, caracterizadas quanto sua morfologia, congeladas e incubadas com anticorpo anti-alfa-6 integrina para a purificação das SSCs por separação celular ativada por fluorescência (FACS). Células testiculares foram geneticamente modificadas com a inserção do gene marcador LacZ e o transplante através dos ductos eferentes foi padronizado. As Células germinativas testiculares foram dissociadas e cultivadas in vitro, porém a viabilidade foi aquém da desejada, inviabilizando as etapas de transformação, transplante e posterior avaliação histológica. Usando o marcador molecular alfa-6 integrina foi possível separar populações de células germinativas testiculares por FACS e a expressão gênica de ITG&alpha;6, GFR&alpha;1, Oct-4 e Thy-1 foi detectada por RT-PCR quantitativo. Em conclusão, não foi possível comprovar a eficiência de transdução e colonização em túbulos seminíferos por células-tronco espermatogoniais selecionadas com alfa-6 integrina. / Throughout the reproductive life of adult males, spermatozoa are formed from spermatogonial stem cells (SSCs) by a process known as spermatogenesis. The in vitro culture of SSCs created new possibilities for transgenesis, however the protocols require addition of growth factors, which increases the maintenance costs of these cells for a prolonged time, making of the cryopreservation of SSCs an alternative for this problem. The molecular phenotype of spermatogonial stem cells have been target of studies in recent decades. One of the most studied marker molecule in the characterization of spermatogonia is integrin alpha-6. Based on these informations, the following hypothesis was proposed: SSCs that show increased expression of integrin alpha-6 are more efficient for genetic modification and colonization of seminiferous tubules. In order to test this hypotesis, murine SSCs were dissociated from testes of 8 to 11 days old mice. These cells were in vitro cultured, characterized based on its morphology, frozen and incubated with anti-integrin alpha-6 antibody for the purification of SSCs by activated cell sorting fluorescence (FACS). Testicular cells were genetically modified with the insertion of the marker gene LacZ and transplantation through the efferent ducts was standardized. The testicular germ cells were dissociated and in vitro cultured, however viability was below expected, precluding the steps of transformation, transplantation and subsequent histological evaluation. Using molecular marker integrin alpha-6 it was possible to separate testicular germ cell populations by FACS and gene expression of ITG&alpha;6, GFR&alpha;1, Oct-4 and Thy-1was detected by quantitative RT-PCR. In conclusion, it was not possible to prove the efficiency of transduction and colonization in the seminiferous tubules by spermatogonial stem cells selected with alpha 6 integrin.