isolation of mononuclear cells from whole blood to obtain induced microglia-like cells for brain research

Entwicklung von blutinduzierten Mikroglia-ähnlichen Zellen zur Erforschung von Erkrankungen des menschlichen Gehirns

In recent years, brain inflammation has been suggested to assume pivotal roles in the pathophysiology of various brain and neuropsychiatric disorders; the microglia have been highlighted as key immunomodulatory cells by human postmortem brain analysis and positron emission tomography (PET)-based bio-imaging techniques1,2,3,4. Postmortem brain and PET imaging analyses reveal significant findings; nevertheless, however, these approaches are inefficient in terms of capturing the dynamic molecular activities of human microglia in the brain in their entirety. Therefore, novel strategies are required to enable the comprehensive evaluation of human microglial functions and dysfunctions at the molecular and cellular levels.
In 2014, we originally engineered a novel technique to produce directly induced microglia-like(iMG) cells5,6, prior to the first publication of human-induced pluripotent stem cell (iPSC)-derived microglia-like cells in 20167. In just 2 weeks, we successfully converted human peripheral blood monocytes into iMG cells by optimizing the cytokines, granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin 34 (IL-34). When we developed this technique, the innovative reprogramming method of inducing neuronal cells from iPS cells or fibroblasts was just beginning to prevail in the world8,9,10,11. However, at that time, a method for inducing iPS-derived microglial cells had not yet been reported, and the generation of a human somatic cell-derived microglial model was desired. Since cytokines such as GM-CSF and IL-34, macrophage colony-stimulating factor, were reported to be necessary for the development and maintenance of microglia12,13,14,15, we hypothesized that a combination of these cytokines could be applied directly to generate a microglial cellular model from blood monocytes. Finally, we succeeded in developing a model of microglia derived from monocytes by combining GM-CSF and IL-345. In addition, some of these combinations of cytokines are also employed to induce microglia from iPS cells7,16 and are assumed to be an important factor in acquiring microglial characteristics.
In contrast to iPSC methods, iMG cells do not require any genetic modification and can be generated in a very short time by simple chemical induction, resulting in lower time and financial costs. Furthermore, iMG cells do not require genetic reprogramming, so we believe that iMG cells are potent surrogate cells to evaluate not only the traits but also the states of human microglia. In the initial paper on the iMG technique in 2014, we confirmed that iMG cells exhibit a phenotype of human microglia, which can be distinct from monocytes and macrophages. For example, iMG cells exhibited an overexpression ratio of CX3C chemokine receptor 1 (CX3CR1) and C-C chemokine receptor type 2 (CCR2) than monocytes and typical microglia markers, including transmembrane protein 119(TMEM 119) and purinergic receptor P2RY125,17. Recently, we validated that peripheral blood-derived iMG cells resemble brain microglia in their gene expression profile of well-known microglial markers in the same patient who underwent brain surgeries18. The iMG cells can be analyzed for dynamic functions at the molecular level, such as phagocytosis and cytokine production, and are expected to compensate for the disadvantages of postmortem brain research and PET studies.
We have discovered previously unknown dynamic pathophysiological mechanisms involving microglia in patients diagnosed with Nasu-Hakola disease5, fibromyalgia19, bipolar disorder20,21, or Moyamoya disease22. Furthermore, based on our original methodology, various laboratories have employed the iMG cells (certain laboratories have designated alternative names to these cells) as a crucial reverse-translational research tool23,24,25,26,27. Sellgren et al. successfully generated iMG cells in compliance with our recommendations and conducted a microarray analysis, which revealed that these cells closely resemble human brain microglia23. Recently, we confirmed the resemblance between human iMG cells and brain primary microglia using RNA sequencing18.
This study aimed to document the methodology to generate iMG cells from human peripheral blood to facilitate reverse-translational research focused on neuropsychiatric diseases. This technique presents potential as a reasonable analytical tool that can effortlessly produce microglial cellular models in a brief duration, even in ill-equipped laboratories that lack gene transfer apparatus or proficient personnel.

Autor im Rampenlicht: Induzierte Mikroglia-ähnliche Zelltechnologie zur Aufklärung der Rolle der mikroglialen Dysfunktion bei neuropsychiatrischen Erkrankungen

Engineering von humanen blutinduzierten Mikroglia-ähnlichen Zellen für die reverse-translationale Hirnforschung

Our lab at Kyushu University aimed to clarify the roles of microglial dysfunction in various neuropsychiatric disorders. We believe that our iMG cell technology will shed new light on microglial dynamic function and dysfunction at the cellular level in human beyond the limitation of human brain analysis, such as postmortem study and also pet brain studies. Even now, animal experiments are essential to clarify the brain pathophysiology of mental disorders, but it is unclear how well rodent data can be applied to human pathophysiology.Our human blood-induced iMG cell technology will this gap between rodent data, clinical data, and microglial function and/or dysfunction. Other human-derived cellular disease model, human iPS cell-derived microglia cells are also developed, which need much time and much money to develop and can assess trait markers but not state markers. The advantage of our iMG method is that it is much simpler, less time-consuming, and cost-effective.We have already revealed several candidate molecular factors by our reverse translational iMG research focusing on neuropsychiatric disorders such as dementia disease, bipolar disorder, fibromyalgia, glioma, and disease. We believe that our iMG cell technology will shed new light on microglial dynamic function and dysfunction at the cellular levels in various neuropsychiatric disorders.

Isolierung mononukleärer Zellen aus Vollblut zur Gewinnung induzierter Mikroglia-ähnlicher Zellen für die Hirnforschung

Geben Sie zunächst 15 Milliliter des Dichtegradientenmediums in ein 15-Milliliter-Zentrifugationsröhrchen und drehen Sie es eine Minute lang bei 1.000 g bei 20 Grad Celsius. Drehen Sie das Röhrchen mit dem in Heparin gesammelten menschlichen Blut um und entfernen Sie mit einer feuersterilisierten Pinzette den Deckel vom Blutentnahmeröhrchen. Geben Sie etwa 10 bis 15 Milliliter Blut in das Dichtegradientenmedium in das Röhrchen.Stellen Sie die Verzögerungsstufe der Zentrifuge auf eins ein und zentrifugieren Sie das Röhrchen mit Blut bei 1.000 g für 10 Minuten bei Raumtemperatur. Entferne die oberste Plasmaschicht bis zu einem Zentimeter über dem Buffy Coat. Der restliche Überstand aus dem Zentrifugationsröhrchen wird in ein anderes Zentrifugenröhrchen mit 10 Millilitern PBS umgefüllt.Die Verzögerungsstufe der Zentrifuge auf drei zurücksetzen und das Röhrchen mit PBS und Überstand zentrifugieren. Saugen Sie den Überstand an und klopfen Sie vorsichtig auf das Rohr, um das Kügelchen zu lösen. Geben Sie anschließend 13 Milliliter Isolationsmedium in das Zentrifugenröhrchen und waschen Sie die Innenwand, um die Zellen richtig zu sammeln.Positionieren Sie mit einer feuersterilisierten Pinzette ein 100-Mikrometer-Zellensieb auf dem konischen 15-Milliliter-Röhrchen. Anschließend filtrieren Sie die Zellsuspension durch das Zellsieb in das konische 15-Milliliter-Röhrchen. Geben Sie die gleichen Mengen der Zellsuspension in zwei konische 15-Milliliter-Röhrchen ab.Listen Sie die Zellen auf, um die entsprechende Konzentration des Isolationspuffers zu berechnen. Pelletieren Sie die Zellen bei 250 G für 10 Minuten bei vier Grad Celsius. Nachdem Sie den Überstand entfernt haben, fügen Sie die entsprechende Menge Isolationspuffer hinzu und pipettieren Sie etwa 20 Mal, um das Pellet zu lösen.

Research

JoVE Journal

Immunology and Infection

Isolation of Mononuclear Cells from Whole Blood to Obtain Induced Microglia-Like Cells for Brain Research

Developing Blood-Induced Microglia-Like Cells for Studying Human Brain Disorders

Engineering of Human Blood-Induced Microglia-like Cells for Reverse-Translational Brain Research

Author Spotlight: Induced Microglia-Like Cell Technology to Shed Light on the Role of Microglial Dysfunction in Neuropsychiatric Disorders

Recent investigations employing animal models have highlighted the significance of microglia as crucial immunological modulators in various ...

Forschung

Immunologie und Infektion

Obtaining Induced Microglia-Like Cells from Whole-Blood Derived Monocytes for Probing Microglial Dynamics in Human Diseases

Gewinnung induzierter Mikroglia-ähnlicher Zellen aus Monozyten aus Vollblut zur Untersuchung der Mikrogliadynamik bei menschlichen Krankheiten 