Ibrahim E. Efe

Dr. Ibrahim E. Efe

Charite, Berlin, Germany
orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 2019 in Cell Reports
Verified
Journal Article
Open access
ABAlice Buonfiglioli
Alice Buonfiglioli
IEIbrahim E. Efe
Ibrahim E. Efe
DGDilansu Guneykaya
Dilansu Guneykaya
AIAndranik Ivanov
Andranik Ivanov
YHYimin Huang
Yimin Huang
SLSeija Lehnardt
Seija Lehnardt
Microglia express Toll-like receptors (TLRs) that sense pathogen- and host-derived factors, including single-stranded RNA. In the brain, let-7 microRNA (miRNA) family members are abundantly expressed, and some have recently been shown to serve as TLR7 ligands. We investigated whether let-7 miRNA family members differentially control microglia biology in health and disease. We found that a subset of let-7 miRNA family members function as signaling molecules to induce microglial release of inflammatory cytokines, modulate antigen presentation, and attenuate cell migration in a TLR7-dependent manner. The capability of the let-7 miRNAs to control microglial function is sequence specific, mapping to a let-7 UUGU motif. In human and murine glioblastoma/glioma, let-7 miRNAs are differentially expressed and reduce murine GL261 glioma growth in the same sequence-specific fashion through microglial TLR7. Taken together, these data establish let-7 miRNAs as key TLR7 signaling activators that serve to regulate the diverse functions of microglia in health and glioma.

27 June 2024 in Brain Sciences
Verified
Journal Article
Open access
PDF file
Manuel De Jesus Encarnacion RamirezManuel De Jesus Encarnacion Ramirez
Manuel De Jesus Encarnacion Ramirez
GCGennady Chmutin
Gennady Chmutin
RNRenat Nurmukhametov
Renat Nurmukhametov
GSGervith Reyes Soto
Gervith Reyes Soto
SKSiddarth Kannan
Siddarth Kannan
Nicola MontemurroNicola Montemurro
Nicola Montemurro
Introduction: The integration of augmented reality (AR) in spine surgery marks a significant advancement, enhancing surgical precision and patient outcomes. AR provides immersive, three-dimensional visualizations of anatomical structures, facilitating meticulous planning and execution of spine surgeries. This technology not only improves spatial understanding and real-time navigation during procedures but also aims to reduce surgical invasiveness and operative times. Despite its potential, challenges such as model accuracy, user interface design, and the learning curve for new technology must be addressed. AR’s application extends beyond the operating room, offering valuable tools for medical education and improving patient communication and satisfaction. Material and methods: A literature review was conducted by searching PubMed and Scopus databases using keywords related to augmented reality in spine surgery, covering publications from January 2020 to January 2024. Results: In total, 319 articles were identified through the initial search of the databases. After screening titles and abstracts, 11 articles in total were included in the qualitative synthesis. Conclusion: Augmented reality (AR) is becoming a transformative force in spine surgery, enhancing precision, education, and outcomes despite hurdles like technical limitations and integration challenges. AR’s immersive visualizations and educational innovations, coupled with its potential synergy with AI and machine learning, indicate a bright future for surgical care. Despite the existing obstacles, AR’s impact on improving surgical accuracy and safety marks a significant leap forward in patient treatment and care.

1 August 2020 in World Neurosurgery
Verified
Journal Article
Closed access
IEIbrahim E. Efe
Ibrahim E. Efe
OAOrhun Utku Aydin
Orhun Utku Aydin
AAAlper Alabulut
Alper Alabulut
OCOzgur Celik
Ozgur Celik
KAKerameddin Aydin
Kerameddin Aydin

6 July 2020 in Journal of Neuroscience
Verified
Journal Article
Closed access
PDF file
YHYimin Huang
Yimin Huang
QZQuan Zhang
Quan Zhang
MLMalgorzata Lubas
Malgorzata Lubas
YYYang Yuan
Yang Yuan
FYFatih Yalcin
Fatih Yalcin
HKHelmut Kettenmann
Helmut Kettenmann
In murine experimental glioma models, TLR3 or TLR9 activation of microglial/macrophages has been shown to impair glioma growth, which could, however, not been verified in recent clinical trials. We therefore tested whether combined TLR3 and TLR9 activation of microglia/macrophages would have a synergistic effect. Indeed, combined TLR3/TLR9 activation augmented the suppression of glioma growth in organotypic brain slices from male mice in a microglia-dependent fashion, and this synergistic suppression depended on interferon β release and phagocytic tumor clearance. Combined TLR3/TLR9 stimulation also augmented several functional features of microglia, such as the release of proinflammatory factors, motility, and phagocytosis activity. TLR3/TLR9 stimulation combined with CD47 blockade further augmented glioma clearance. Finally, we confirmed that the coactivation of TLR3/TLR9 also augments the impairment of glioma growth in vivo. Our results show that combined activation of TLR3/TLR9 in microglia/macrophages results in a more efficient glioma suppression, which may provide a potential strategy for glioma treatment. SIGNIFICANCE STATEMENT Glioma-associated microglia/macrophages (GAMs) are the predominant immune cells in glioma growth and are recently considered as antitumor targets. TLRs are involved in glioma growth, but the TLR3 or TLR9 ligands were not successful in clinical trials in treating glioma. We therefore combined TLR3 and TLR9 activation of GAMs, resulting in a strong synergistic effect of tumor clearance in vitro, ex vivo, and in vivo. Mechanisms of this GAM-glioma interaction involve IFNβ signaling and increased tumor clearance by GAMs. Interfering with CD47 signaling had an additional impact on tumor clearance. We propose that these signaling pathways could be exploited as anti-glioma targets.

30 July 2022 in Cureus
Verified
Journal Article
Open access
Manuel De Jesus Encarnacion RamirezManuel De Jesus Encarnacion Ramirez
Manuel De Jesus Encarnacion Ramirez
RNRenat Nurmukhametov
Renat Nurmukhametov
GMGerald Musa
Gerald Musa
RCRossi Evelyn Barrientos Castillo
Rossi Evelyn Barrientos Castillo
VEValerin L. Arno Encarnacion
Valerin L. Arno Encarnacion
IEIbrahim E. Efe
Ibrahim E. Efe
Cadaveric models remain an essential part of medical training across all specialties. Due to their scarcity, high costs, and possible health hazards, there is a need for more accessible and affordable alternatives, especially in low-resource settings. We introduce cost-effective and easily replicable three-dimensional (3D) printed models to help democratize access to hands-on neuroanatomy education. Silicone-based glue is applied on the surface of a 3D-printed or cadaveric bone frame. Using plastiline on a 3 mm 3D acrylonitrile butadiene styrene pen, the desired anatomical structure is printed on the bone frame. A heat gun is used to smoothen the plastic edges. The structure can then be painted according to its appearance in the real anatomy. Using this technique, we successfully generated a variety of anatomical models to study the cerebrovascular anatomy, the course of the cranial nerves in relation to the skull base, and extracranial structures including the spine. Procurement and conservation of cadaveric specimens can be cumbersome. Our model may be an affordable and easily replicable approach to bridging the gap in anatomy education between low- and high-resource facilities.

31 October 2022 in Neurology International
Verified
Journal Article
Open access
PDF file
JRJuan Pablo Reynoso
Juan Pablo Reynoso
Manuel De Jesus Encarnacion RamirezManuel De Jesus Encarnacion Ramirez
Manuel De Jesus Encarnacion Ramirez
RNRenat Nurmukhametov
Renat Nurmukhametov
DMDmitry Melchenko
Dmitry Melchenko
IEIbrahim E. Efe
Ibrahim E. Efe
Nicola MontemurroNicola Montemurro
Nicola Montemurro
Background: The sciatic nerve (SN) is the widest nerve of the human body that exits the pelvis through the greater sciatic foramen, usually below the piriformis muscle (PM), and descends between the greater trochanter of the femur and ischial tuberosity of the pelvis to the knee. The aim of this paper is to examine and identify the SN variations in relation to the PM, its prevalence, pattern, and course. Methods: A prospective-descriptive cross-sectional study was carried out to determine the frequency of anatomical variations in the exit of the SN in relation with the PM in 20 anatomical bodies (corpses) of both genders, in equal numbers. Results: The dissection of 40 SNs in corpses of both sexes in equal numbers showed that the SN exited inferior to the PM in 37 lower limbs (92.5%); between the fascicles of the PM and inferior to the PM in two lower limbs (5%); and in one thigh, between the fascicles of the PM and superior to the PM (2.5%). Our study reported that the SN divides in its terminal branches more commonly in the proximal part of the popliteal fossa in 55% of cases, in the gluteal region in 35% of cases, and in the middle third of the thigh in 10% of cases. Conclusions: Anatomical variations of the SN in relation to the PM are challenging for the diagnostic and therapeutic procedure in many clinical and surgical cases. Rapid recognition of the SN changes makes surgical approaches more accurate and effective. Our study confirmed that the SN exits the pelvis most commonly below the PM, although some anatomical variations may occur.