Migratory Stream Research Articles

Migration scale, process, and impact in the Tiwanaku colonies: Paleomobility at the archaeological site of Omo M10.

Contemporary migrations show form and intensity of interaction between homeland and host communities to shape social dynamics and identities. We apply here a contemporary theoretical framework and biogeochemical analyses to elucidate the scale, processes, and impacts of migration in the Tiwanaku polity (6th-11th c. CE) by inferring the mobility of individuals interred at the Tiwanaku-affiliated site of Omo M10 (Moquegua Valley, Peru). For each of 124 individuals, we captured paleomobility across the life-course by analyzing up to four enamel and bone samples that formed during discrete developmental periods for radiogenic strontium (87Sr/86Sr) and stable oxygen (δ18Ocarbonate(VPDB)) isotopes. At Omo M10, archaeological human enamel and bone values range from 87Sr/86Sr = 0.70632-0.72183 and δ18Ocarbonate(VPDB) = -13.4‰ to +1.7‰, with a mean of 87Sr/86Sr = 0.70763 ± 0.00164 (1σ, n = 334) and δ18O = -7.8‰ ± 1.9‰ (1σ, n = 334). Together with archaeological evidence, we interpret these data as evidence for multigenerational interaction between communities in the high-altitude Tiwanaku heartland and at the site of Omo M10. Our results suggest that one-fourth of individuals spent some part of their life outside of Moquegua and one in eight individuals from Omo M10 were first-generation migrants. Greater mobility of females and juveniles at Omo M10 indicates that gender and family were important social constructs in maintaining relationships and cultural continuity in provincial Tiwanaku life, and communities maintained autochthonous migration streams with Tiwanaku-affiliated populations throughout the south-central Andes. Intra-individual biogeochemical analyses of migration at Omo M10 contribute a nuanced perspective on the diverse experiences of multigenerational Tiwanaku colonies.

Effect of microwave radiation on adult neurogenesis and behavior of prenatally exposed rats

Postnatal neurogenesis appears to be highly sensitive to environmental factors, including microwave electromagnetic radiation (MWR). Here, we investigated the impact of MWR during intrauterine development on juvenile and adult neurogenesis in the rostral migratory stream (RMS) and the dentate gyrus of the hippocampus in the rat brain, as well as its effect on animal behavior. Female rats were exposed to MWR at a frequency of 2.45 GHz for 2 hours daily throughout pregnancy. The offspring of irradiated mothers survived to either juvenile age or adulthood. The brains of the rats were subjected to morphological analysis, assessing cell proliferation and death in both neurogenic regions. In the RMS, the differentiation of nitrergic neurons was also investigated. The effect of MWR on behavior was evaluated in rats surviving to adulthood. Prenatal MWR exposure caused significant changes in the number of proliferating and dying cells, depending on the age of the animals and the observed neurogenic region. In addition, MWR attenuated the maturation of nitrergic neurons in the RMS in both juvenile and adult rats. Morphological alterations in neurogenesis were accompanied by changes in animals’ behavior. Affected neurogenesis and changes in animal behavior suggest a high sensitivity of the developing brain to MWR.

The effects of Atoh8 on postnatal murine neurogenesis.

Introduction Basic helix-loop-helix (bHLH) transcription factors are expressed in various organs and are involved in diverse developmental processes. The mouse atonal homolog 8 (Atoh8), a bHLH transcription factor plays a crucial role in various developmental processes, especially as a regulator of neurogenesis in the retina. Besides, Atoh8 expression has been observed in the central nervous system. The function of Atoh8 during the postnatal neurogenesis is still unclear. Methods This study focuses on elucidating the impact of Atoh8 on postnatal neurogenesis in the brain, particularly in selected regions; the subventricular zone (SVZ), rostral migration stream (RMS) and olfactory bulb (OB), across different life stages, using male homozygous Atoh8-knockout (M6KO) mice. Our morphometric analysis is based on immunohistochemically labeled markers for neuroblasts (Doublecortin) and proliferation (Phospho-Histone H3, PHH3) as well as pan neuronal markers. Results In Atoh8-/- mice alteration in the postnatal neurogenesis can be observed. Immunohistochemical analysis revealed a significant reduction in doublecortin-positive neuroblasts within the SVZ of neonatal M6KO mice compared to wildtype (WT) mice. Interestingly, no differences in cell number and distribution was observed in the subsequent migration of neuroblasts through the rostral migration stream (RMS) to the olfactory bulb (OB). Proliferating PHH3-positive neuronal progenitor cells were significantly diminished in proliferation rate in both the SVZ and RMS of neonatal and young M6KO mice. Furthermore, in the glomerular layer of the OB significantly fewer neurons were detected in the neonatal stage. Conclusion In conclusion, Atoh8 emerges as a positive regulator of postnatal neurogenesis in the brain. Its role encompasses the promotion of neuroblast formation, modulation of proliferation rates, differentiation, and maintenance of mature neurons. Understanding the intricacies of Atoh8 function provides valuable insights into the complex regulatory mechanisms governing neurogenesis.

Unidirectional dispersal of blow fly larvae following decomposition fluids from a pig carcass

The decomposition of a body, and the associated gaseous and liquid discharges emanating from it, attract gravid female blow flies which lay their eggs in or on the body. After the eggs have hatched, the emerging larvae start feeding on the body. As decomposition progresses, the blow fly larvae often migrate away, typically in a random manner in search of favourable conditions for pupation. In this paper, we report on a rarely described phenomenon of unidirectional mass migration of blow fly larvae and postulate on the factors which may drive this process. A decomposition trial utilising a 60-kg pig carcass, deployed in the summer months in Table Mountain National Park, Cape Town, South Africa, was conducted in 2022. On the fifth day of the trial, simultaneous unidirectional mass dispersal of blow fly larvae was observed. The larvae moved downhill in a southeasterly direction, following the flow of decomposition fluids oozing out from the pig carcass. The ‘larval migration stream’ had a length of approximately 1.5 m with a width of 40 cm, tapering to 17 cm at the terminal point. The larval migration stream consisted of the larvae of Chrysomya albiceps and Chrysomya chloropyga. This study demonstrates the importance of understanding the timing and pattern of dispersal of post-feeding blow fly larvae in each geographical region. This is crucial as the minimum post-mortem interval can be miscalculated if older immature insects dispersing from the corpse are not considered and collected during crime scene investigations.

Impaired olfactory performance and anxiety-like behavior in a rat model of multiple sclerosis are associated with enhanced adenosine signaling in the olfactory bulb via A1R, A2BR, and A3R.

The present study shows that animals with experimental autoimmune encephalomyelitis (EAE) exhibit olfactory dysfunction and impaired general cognitive abilities, as well as anxiety-like behavior. Olfactory dysfunction occurs on average at 2 dpi, well before the onset of the first motor signs of EAE (8-10 dpi). After the initial olfactory dysfunction, the EAE animals show a fluctuation in olfactory performance that resembles the relapsing-remitting course of human MS. The study also shows severe neuroinflammation in the olfactory bulb (OB), with numerous infiltrated CD4+ T cells and peripheral macrophages in the superficial OB layers, marked microgliosis, and massive induction of TNF-α, IL-1β, and IL-6. Reduced tyrosine hydroxylase activity in the glomerular layer, pronounced granule cell atrophy, and reduced numbers of type B neuroblasts in the rostral migratory stream also indicate altered plasticity of the neuronal network in the OB. Considering the exceptionally high purinome expression in the OB, the possible involvement of purinergic signaling was also investigated. The study shows that macrophages infiltrating the OB overexpress A3R, while highly reactive microglia overexpress the adenosine-producing enzyme eN/CD73 as well as A2BR, A3R, and P2X4R. Given the simultaneous induction of complement component C3, the results suggest that the microglial cells develop a functional phenotype of phagocytizing microglia. The study also demonstrates transcriptional and translational upregulation of A1R in mitral and tufted cells, which likely influence resting network activity in OB and likely contribute to olfactory dysfunction in EAE. Overall, our study shows that olfactory dysfunction and altered social and cognitive behavior in EAE are associated with increased adenosine signaling via A1R, A2BR, and A3R.

Social support and economic conditions among older migrants in India: do distance, duration, and streams of migration play a role in later life?

BackgroundBeing older and having a migrant feature might cause a double risk of vulnerability in poor economic, social support, and health status at the place of destination. This study examines the association of migration on the social support and economic condition of older persons in India.MethodsLongitudinal Ageing Study in India (LASI) wave-I (2017–2018) data with total samples of 66,156 older adults aged 45 + with 30,869 and 35,287 male and female samples, respectively, used in this study. Descriptive and bivariate analyses have been performed to examine the pattern of older migrants, and multinomial logistic regression analysis has been used to establish the associations between migration, social support, and economic condition.ResultsOver half (57.5%) of the population aged 45 + in India had migrant characteristics; 80% migrated before 25 years. Of all migrants, about 90% migrated within one state (Intrastate), and 9% migrated to another (Interstate). The association between social support and migration by distance and the adjusted result showed that immigrants were less likely to have medium [RRR = 0.56 (CI; 0.46–0.68)] and high [RRR = 0.39 (CI; 0.30–0.50)] social support. The interstate migrants were also less likely to have high [RRR = 0.90 (CI; 0.83–0.98)] social support. The migrants with 0–9 years of duration were less likely to have high social support, and the urban to rural stream migrants were more likely to have high social support. The association between economic status and migration by distance and the adjusted result showed that more affluent immigrants were likelier to have [RRR = 1.41 (CI; 1.14–1.73)] better economic conditions than affluent non-migrants. Migrants with 0–9-year duration and urban to rural stream were found to be likelier to have better economic conditions.ConclusionsThe findings of this study suggest that distance, duration, and migration stream have a significant association with social support and economic conditions in later life. In exploring migration’s effect on social and economic status, policymakers should prioritize migrants in their agenda to maintain socio-economic and social support for older persons in India to achieve the sustainable goal of active and healthy ageing.

FMRP regulates postnatal neuronal migration via MAP1B.

The fragile X syndrome (FXS) represents the most prevalent form of inherited intellectual disability and is the first monogenic cause of autism spectrum disorder. FXS results from the absence of the RNA-binding protein FMRP (fragile X messenger ribonucleoprotein). Neuronal migration is an essential step of brain development allowing displacement of neurons from their germinal niches to their final integration site. The precise role of FMRP in neuronal migration remains largely unexplored. Using live imaging of postnatal rostral migratory stream (RMS) neurons in Fmr1-null mice, we observed that the absence of FMRP leads to delayed neuronal migration and altered trajectory, associated with defects of centrosomal movement. RNA-interference-induced knockdown of Fmr1 shows that these migratory defects are cell-autonomous. Notably, the primary Fmrp mRNA target implicated in these migratory defects is microtubule-associated protein 1B (MAP1B). Knocking down MAP1B expression effectively rescued most of the observed migratory defects. Finally, we elucidate the molecular mechanisms at play by demonstrating that the absence of FMRP induces defects in the cage of microtubules surrounding the nucleus of migrating neurons, which is rescued by MAP1B knockdown. Our findings reveal a novel neurodevelopmental role for FMRP in collaboration with MAP1B, jointly orchestrating neuronal migration by influencing the microtubular cytoskeleton.

FMRP regulates postnatal neuronal migration via MAP1B

FMRP regulates postnatal neuronal migration via MAP1B

Impact of subthalamic nucleus deep brain stimulation at different frequencies on neurogenesis in a rat model of Parkinson's disease

Neurogenesis, play a vital role in neuronal plasticity of adult mammalian brains, and its dysregulation is present in the pathophysiology of Parkinson's disease (PD). While subthalamic nucleus deep brain stimulation (STN-DBS) at various frequencies has been proven effective in alleviating PD symptoms, its influence on neurogenesis remains unclear. This study aimed to investigate the effects of 1-week electrical stimulation at frequencies of 60Hz, 130Hz, and 180Hz on neurogenesis in the subventricular zone (SVZ) of PD rats. A hemiparkinsonian rat model was established using 6-hydroxydopamine and categorized into six groups: control, PD, sham stimulation, 60Hz stimulation, 130Hz stimulation, and 180Hz stimulation. Motor function was assessed using the open field test and rotarod test after one week of STN-DBS at different frequencies. Tyrosine hydroxylase (TH) expression in brain tissue was analyzed via Western blot and immunohistochemistry. Immunofluorescence analysis was conducted to evaluate the expression of BrdU/Sox2, BrdU/GFAP, Ki67/GFAP, and BrdU/DCX in bilateral SVZ and the rostral migratory stream (RMS). Our findings revealed that high-frequency STN-DBS improved motor function. Specifically, stimulation at 130Hz increased dopaminergic neuron survival in the PD rat model, while significantly enhancing the proliferation of neural stem cells (NSCs) and neuroblasts in bilateral SVZ. Moreover, this stimulation effectively facilitated the generation of new NSCs in the ipsilateral RMS and triggered the emergence of fresh neuroblasts in bilateral RMS, with notable presence within the lesioned striatum. Conversely, electrical stimulation at 60Hz and 180Hz did not exhibit comparable effects. The observed promotion of neurogenesis in PD rats following STN-DBS provides valuable insights into the mechanistic basis of this therapeutic approach for PD.

Evaluating neural crest cell migration in a Col4a1 mutant mouse model of ocular anterior segment dysgenesis

The periocular mesenchyme (POM) is a transient migratory embryonic tissue derived from neural crest cells (NCCs) and paraxial mesoderm that gives rise to most of the structures in front of the eye. Morphogenetic defects of these structures can impair aqueous humor outflow, leading to elevated intraocular pressure and glaucoma. Mutations in collagen type IV alpha 1 (COL4A1) and alpha 2 (COL4A2) cause Gould syndrome – a multisystem disorder often characterized by variable cerebrovascular, ocular, renal, and neuromuscular manifestations. Approximately one-third of individuals with COL4A1 and COL4A2 mutations have ocular anterior segment dysgenesis (ASD), including congenital glaucoma resulting from abnormalities of POM-derived structures. POM differentiation has been a major focus of ASD research, but the underlying cellular mechanisms are still unclear. Moreover, earlier events including NCC migration and survival defects have been implicated in ASD; however, their roles are not as well understood. Vascular defects are among the most common consequences of COL4A1 and COL4A2 mutations and can influence NCC survival and migration. We therefore hypothesized that NCC migration might be impaired by COL4A1 and COL4A2 mutations. In this study, we used 3D confocal microscopy, gross morphology, and quantitative analyses to test NCC migration in Col4a1 mutant mice. We show that homozygous Col4a1 mutant embryos have severe embryonic growth retardation and lethality, and we identified a potential maternal effect on embryo development. Cerebrovascular defects in heterozygous Col4a1 mutant embryos were present as early as E9.0, showing abnormal cerebral vasculature plexus remodeling compared to controls. We detected abnormal NCC migration within the diencephalic stream and the POM in heterozygous Col4a1 mutants whereby mutant NCCs formed smaller diencephalic migratory streams and POMs. In these settings, migratory NCCs within the diencephalic stream and POM localize farther away from the developing vasculature. Our results show for the first time that Col4a1 mutations lead to cranial NCCs migratory defects in the context of early onset defective angiogenesis without affecting cell numbers, possibly impacting the relation between NCCs and the blood vessels during ASD development.

Sensory Stimulation-dependent Npas4 Expression in the Olfactory Bulb during Early Postnatal Development.

The development of the olfactory system is influenced by sensory inputs, and it maintains neuronal generation and plasticity throughout the lifespan. The olfactory bulb contains a higher proportion of interneurons than other brain regions, particularly during the early postnatal period of neurogenesis. Although the relationship between sensory stimulation and olfactory bulb development during the postnatal period has been well studied, the molecular mechanisms have yet to be identified. In this study, we used western blotting and immunohistochemistry to analyze the expression of the transcription factor Npas4, a neuron-specific immediate-early gene that acts as a developmental regulator in many brain regions. We found that Npas4 is highly expressed in olfactory bulb interneurons during the early postnatal stages and gradually decreases toward the late postnatal stages. Npas4 expression was observed in all olfactory bulb layers, including the rostral migratory stream, where newborn neurons are generated and migrate to the olfactory bulb. Under sensory deprivation, the olfactory bulb size and the number of olfactory bulb interneurons were reduced. Furthermore, Npas4 expression and the expression of putative Npas4 downstream molecules were decreased. Collectively, these findings indicate that Npas4 expression induced by sensory input plays a role in the formation of neural circuits with excitatory mitral/tufted cells by regulating the survival of olfactory bulb interneurons during the early stages of postnatal development.

Olfactory bulb anomalies in KBG syndrome mouse model and patients

ANKRD11 (ankyrin repeat domain 11) is a chromatin regulator and the only gene associated with KBG syndrome, a rare neurodevelopmental disorder. We have previously shown that Ankrd11 regulates murine embryonic cortical neurogenesis. Here, we show a novel olfactory bulb phenotype in a KBG syndrome mouse model and two diagnosed patients. Conditional knockout of Ankrd11 in murine embryonic neural stem cells leads to aberrant postnatal olfactory bulb development and reduced size due to reduction of the olfactory bulb granule cell layer. We further show that the rostral migratory stream has incomplete migration of neuroblasts, reduced cell proliferation as well as aberrant differentiation of neurons. This leads to reduced neuroblasts and neurons in the olfactory bulb granule cell layer. In vitro, Ankrd11-deficient neural stem cells from the postnatal subventricular zone display reduced migration, proliferation, and neurogenesis. Finally, we describe two clinically and molecularly confirmed KBG syndrome patients with anosmia and olfactory bulb and groove hypo-dysgenesis/agenesis. Our report provides evidence that Ankrd11 is a novel regulator of olfactory bulb development and neuroblast migration. Moreover, our study highlights a novel clinical sign of KBG syndrome linked to ANKRD11 perturbations in mice and humans.

Wpływ płci na doświadczenia migracyjne Polaków w Niemczech. Przykład Berlina i Hamburga

Gender influences most aspects of migration, placing migrants in slightly different positions in the host country. Gender differences are visible not only in masculinized or feminized migration streams, but also in those that are balanced in terms of gender ratio. In the case of Polish migrations to Germany, the third type of migration streams dominates. This type of migration is characterized by a relatively equal gender structure of Polish migrants. The main aim of this paper is to identify the migration experiences of Poles in the context of revealing gender differences and their potential impact on everyday life in the host country. The article was prepared based on the results of original quantitative (surveys) and qualitative (in-depth interviews) social research conducted among Polish women and men living in Berlin and Hamburg. The example of Germany as a host country allowed to prove that Polish women and men migrants experience the migration process differently. A significant difference in the context of gender was revealed in the following areas: activity in the public sphere, satisfaction with remuneration and level of knowledge of the German language.

Radiation-induced bystander effect on the brain after fractionated spinal cord irradiation of aging rats

We investigated the influence of the so-called bystander effect on metabolic and histopathological changes in the rat brain after fractionated spinal cord irradiation. The study was initiated with adult Wistar male rats (n = 20) at the age of 9 months. The group designated to irradiation (n = 10) and the age-matched control animals (n = 10) were subjected to an initial measurement using in vivo proton magnetic resonance spectroscopy (1H MRS) and magnetic resonance imaging (MRI). After allowing the animals to survive until 12 months, they received fractionated spinal cord irradiation with a total dose of 24 Gy administered in 3 fractions (8 Gy per fraction) once a week on the same day for 3 consecutive weeks. 1H MRS and MRI of brain metabolites were performed in the hippocampus, corpus striatum, and olfactory bulb (OB) before irradiation (9-month-old rats) and subsequently 48 h (12-month-old) and 2 months (14-month-old) after the completion of irradiation. After the animals were sacrificed at the age of 14 months, brain tissue changes were investigated in two neurogenic regions: the hippocampal dentate gyrus (DG) and the rostral migratory stream (RMS). By comparing the group of 9-month-old rats and individuals measured 48 h (at the age of 12 months) after irradiation, we found a significant decrease in the ratio of total N-acetyl aspartate to total creatine (tNAA/tCr) and gamma-aminobutyric acid to tCr (GABA/tCr) in OB and hippocampus. A significant increase in myoinositol to tCr (mIns/tCr) in the OB persisted up to 14 months of age. Proton nuclear magnetic resonance (1H NMR)-based plasma metabolomics showed a significant increase in keto acids and decreased tyrosine and tricarboxylic cycle enzymes. Morphometric analysis of neurogenic regions of 14-month-old rats showed well-preserved stem cells, neuroblasts, and increased neurodegeneration. The radiation-induced bystander effect more significantly affected metabolite concentration than the distribution of selected cell types.

Histological changes in the olfactory bulb and rostral migratory stream due to interruption of olfactory input

ObjectivePeriglomerular and granule cells in the adult mammalian olfactory bulb modulate olfactory signal transmission. These cells originate from the subventricular zone, migrate to the olfactory bulb via the Rostral Migratory Stream (RMS), and differentiate into mature cells within the olfactory bulb throughout postnatal life. While the regulation of neuroblast development is known to be affected by external stimuli, there is a lack of information concerning changes that occur during the recovery process after injury caused by external stimuli. To address this gap in research, the present study conducted histological observations to investigate changes in the olfactory bulb and RMS occurring after the degeneration and regeneration of olfactory neurons. MethodsTo create a model of olfactory neurodegeneration, adult mice were administered methimazole intraperitoneally. Nasal tissue and whole brains were removed 3, 7, 14 and 28 days after methimazole administration, and EdU was administered 2 and 4 h before removal of these tissues to monitor dividing cells in the RMS. Methimazole-untreated mice were used as controls. Olfactory nerve fibers entering the olfactory glomerulus were observed immunohistochemically using anti-olfactory marker protein. In the brain tissue, the entire RMS was observed and the volume and total number of cells in the RMS were measured. In addition, the number of neuroblasts and dividing neuroblasts passing through the RMS were measured using anti-doublecortin and anti-EdU antibodies, respectively. Statistical analysis was performed using the Tukey test. ResultsOlfactory epithelium degenerated was observed after methimazole administration, and recovered after 28 days. In the olfactory glomeruli, degeneration of OMP fibers began after methimazole administration, and after day 14, OMP fibers were reduced or absent by day 28, and overall OMP positive fibers were less than 20%. Glomerular volume tended to decrease after methimazole administration and did not appear to recover, even 28 days after recovery of the olfactory epithelium. In the RMS, EdU-positive cells decreased on day 3 and began to increase on day 7. However, they did not recover to the same levels as the control methimazole-untreated mice even after 28 days. ConclusionThese results suggest that the division and maturation of neuroblasts migrating from the RMS was suppressed by olfactory nerve degeneration or the disruption of olfactory input.

A Gender-Aware Analysis on the Feminization of Entertainment Industry in Japan

This manuscript reexamines the institutionalization of the feminization of migration industry in the Philippine-Japan migration stream through a gender-aware approach. It interrogates on the reasons why Filipina migrants made their way out of the Philippines, through regular and illicit channels, to a host country like Japan despite its restrictive immigration policies. The study unpacks on the common notion that along with active state facilitation, Filipino women migrants’ mobility or those who are engaged in “nightwork” is basically mediated through the entertainment industry. This research is a product of long engagements with the respondents and various key-informants of NGOs and club owners from 2010 to 2015. The findings reveal that women migrants are able to exploit the migration industry as their personal network in alleviating their precarious status. The researcher agrees that the institutionalization of the migration through the entertainment industry from the Philippines to Japan perpetuates an exploitative woman-dominated migration stream. However, in most instances, Filipina migrants capably exploit their personal or community network formation which could also be found in the nightwork industry.

DEMOGRAPHY OF SOUTHERN UKRAINE IN THE LAST QUARTER OF THE 18 th CENTURY: SCIENTIFIC MODELS AND THE RESULTS OF THEIR IMPLEMENTATION

This article explores the demographic processes in the territories of the former Domain of the Lower Zaporizhian Host of the last quarter of the 18th century. It has been shown that the relevance of this research goes well beyond the scope of demography and is closely related to the modern tendencies of using ‘Novorossiya’ concept. The developed research model is based on information from registers of births, marriages and deaths, as well as on findings, map books and audit evidence and envisages the use of demographic and sociological methods of research of the impact of Zaporizhian Cossacks and various migrant streams on population social structure and of horizontal contacts between its different segments. The reasons arise to explore the fertility dynamics in families representing different social segments: urban commoners, subjects of landlords, the military and their subjects. It has been shown that the fact of excess mortality among the military was enhanced by the effect of restrictions imposed by age peculiarities and ex-soldiers’ matrimonial strategies on natural increase in this social category. Opportunities for expansion in the number of non-Ukrainian population through settlement of the military in the surroundings decreased. Information from registers of births, marriages and deaths about godparents and married couples has enabled the use of M. Granovetter’s option of ‘the Strength of the Weak Ties’ permitting to identify informal small reference groups at the level of populated localities, their role and number in a community, their isolated or open status, formation criteria, number of their members and period of existence. The suggested model offers the possibility to trace the process of ex-Zaporizhian Cossacks transition to other social categories, degree of settlement in a region of influx from various Ukrainian lands as well as from typical Muscovite regions.

‘Away From Home’ - A Systematic Literature Review of the Factors and Challenges of Women Migration

Feminization of Migration refers to the increasing participation of women in long-distance migration, a trend driven by the evolving gender dynamics in the workforce. This shift is characterized by the engagement of women in occupations traditionally perceived as feminine, demanding the presence of women in these sectors. Consequently, the concept of the "Feminization of Migration" has prompted a gender-focused perspective on migration, redirecting attention towards the rights and interests of women within migration streams. Global patterns of women's migration have undergone a transformation, moving beyond the traditional role of women migrating as dependents with their families. Instead, there is a notable trend of women migrating independently, driven by economic motives and assuming the role of primary breadwinners for their families. This shift has not only altered the landscape of migration but has also amplified the presence of women in migration literature and practical policies designed with a gender-responsive approach. In light of these developments, this paper aims to conduct a systematic literature review that explores the factors and challenges associated with women's migration.

Protracted neuronal recruitment in the temporal lobes of young children

The temporal lobe of the human brain contains the entorhinal cortex (EC). This region of the brain is a highly interconnected integrative hub for sensory and spatial information; it also has a key role in episodic memory formation and is the main source of cortical hippocampal inputs1–4. The human EC continues to develop during childhood5, but neurogenesis and neuronal migration to the EC are widely considered to be complete by birth. Here we show that the human temporal lobe contains many young neurons migrating into the postnatal EC and adjacent regions, with a large tangential stream persisting until the age of around one year and radial dispersal continuing until around two to three years of age. By contrast, we found no equivalent postnatal migration in rhesus macaques (Macaca mulatta). Immunostaining and single-nucleus RNA sequencing of ganglionic eminence germinal zones, the EC stream and the postnatal EC revealed that most migrating cells in the EC stream are derived from the caudal ganglionic eminence and become LAMP5+RELN+ inhibitory interneurons. These late-arriving interneurons could continue to shape the processing of sensory and spatial information well into postnatal life, when children are actively interacting with their environment. The EC is one of the first regions of the brain to be affected in Alzheimer’s disease, and previous work has linked cognitive decline to the loss of LAMP5+RELN+ cells6,7. Our investigation reveals that many of these cells arrive in the EC through a major postnatal migratory stream in early childhood.

TMIC-52. HISTONE H3K27ME3 LEVEL GOVERN TUMOR-ASSOCIATED MICROGLIA REPROGRAMMING IN RESPONSE TO GBM

Abstract Glioblastoma (GBM) is the most common malignant primary brain tumor and its invasive nature makes complete dissection difficult. However, how GBM invade in the brain is poorly understood. Although, microglia are the resident immune cells in the brain that can support GBM invasion, their roles are yet elusive. Here, we retraced early steps of GBM invasion and their interaction with tumor-associated microglia (TAM) in a highly infiltrative murine GBM model in immunocompetent background. We show that microglia are activated in a wide tumor field ahead of GBM invasion, followed by glial net formation, encircling invading tumors. Next, physical contacts with GBM cells initiate an astounding morphological, and functional transformation of microglia and marrow-derived macrophages to form collectively organized migration streams with intertwined GBM cells. Here we show that Kdm6b, a H3K27me3 demethylase, is induced in TAMs during this process. Intriguingly, GBM disseminated more widely in juvenile host brains, which was associated with highly induced Kdm6b expression. Moreover, we show that Kdm6b inhibition with small chemical inhibitor GSKJ-4, perturbs TAM reprogramming, and GBM invasion. Together, our data reveal that microglia reprogramming provide directional cues for GBM invasion through epigenetic mechanisms and this may give insights to halt GBM invasion.