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2 calcium-dependent proteins kinases improve maize drought tolerance by simply triggering anion channel ZmSLAC1 in guard tissue.
Mammals have developed bone marrow (BM) inside the bone tissue because of evolution. Now, it appears that bone tissue displays functional communication with the hematopoietic system. Osteoblast lineage cells serve as a part of the microenvironment for immature hematopoietic cells, whereas mature hematopoietic cells play important roles in regulating osteoblast activity. The nervous system maintains the balance between the hematopoietic and skeletal systems. An understanding of the multiple-organ network that exists between the BM and other systems is useful to elucidate phenomena in clinical hematology and even in other fields, an area which I propose to call "marrowlogy."Lymphocytes play pivotal roles in innate and adaptive immunity. The differentiation process by which hematopoietic stem cells (HSCs) acquire specific functions has been extensively investigated and is considered the paradigm of cell differentiation. It has been widely accepted that highly enriched HSCs are heterogeneous with respect to their lymphopoietic potential, and aged or stressed HSCs are skewed to the myeloid lineage. Several transcription factors and cytokine signaling pathways have been reported as essential to lymphocyte differentiation. However, the molecular mechanism that modulates the earliest stage remains unclear. Furthermore, the origin and characteristics of early T-lymphoid progenitors that migrate from the bone marrow to the thymus are still unknown in this field. Epigenetic mechanisms likely influence early lineage specification through the regulation of mitochondrial function and modification of nuclear chromatin structure. This review summarizes previous and recent findings on the processes involved in early lymphocyte differentiation. Thus, it provides a foundation for the understanding of the physiology of HSC aging and the pathology of intractable acute lymphocytic leukemia.A literature review of the data of hematological cancer survivors revealed that both the cumulative proportion and burden of late effects change according to the attained age, primary cancer, and type of treatment. I selected neurocognitive dysfunction, cardiovascular disease, endocrinological dysfunction, musculoskeletal dysfunction, subsequent immunodeficiency, and reproductive dysfunction as representative late effects. I accordingly explained the characteristics of secondary cancers as the most life-threatening late effects and compared the late effects between survivors who did and did not undergo hematopoietic stem cell transplantation, respectively. The main goals of my educational lecture are as follows (1) to highlight important late effects in hematological cancer survivors and their risk factors; (2) to discuss primary secondary cancers and explain their characteristics (e.g., frequency, incubation periods, and risk factors); (3) to characterize late effects after hematopoietic stem cell transplantation; and (4) to use representative long-term follow-up guidelines if necessary.Langerhans cell histiocytosis (LCH) is a rare disease characterized by tissue infiltration of clusters of CD1a+/CD207+ histiocyte-like cells and a resultant surrounding inflammatory reaction. see more Because of its morphological similarity to cutaneous Langerhans cells, LCH was formerly named histiocytosis X in 1987. However, its cell lineage appears closely related to myeloid dendritic cells. In 2010, BRAF-V600E was detected in biopsy specimens from the majority of LCH patients. The subsequent observation of extracellular signal-regulated kinase phosphorylation in almost all LCH samples suggested that LCH was a neoplasm provoked by activation of the mitogen-activated protein (MAP) kinase pathway. Therefore, the 2016 Revised Classification by the Histiocyte Society defined LCH as an inflammatory myeloid neoplasm. Although a series of global and domestic clinical trials have improved the prognosis of pediatric LCH patients, no standard therapy with a high level of evidence for adult cases exists. Generally, LCH patients have a favorable prognosis, but delayed diagnosis and intervention may cause severe damage to the involved organs, resulting in a poor quality of life. Here we present recent advances in the pathophysiology and treatment of LCH to enlighten the understanding of this orphan disease.In 2000, imatinib became the first tyrosine kinase inhibitor (TKI) approved for the treatment of chronic myeloid leukemia (CML); this was soon followed by second generation (nilotinib, dasatinib, and bosutinib) and third generation (ponatinib) TKIs, all of which are currently available for the treatment of CML. Their emergence has revolutionized treatment strategies for CML, leading to a new era that has seen the 10-year overall survival rate for CML patients exceed 80%; despite the impact of TKIs on CML prognosis, only 10 to 20% of CML patients maintain treatment-free remission after TKI cessation. Moreover, prolonged treatment produces various adverse effects, such as serious vascular adverse events including stroke, myocardial infarction, and peripheral arterial occlusive disease. The pathophysiological mechanisms underlying those effects remain unclear, and protocols for managing such life-threatening events have not been established. Thus, I conducted a narrative review of the literature to clarify the current state of knowledge. Based on that review and my experiences during daily clinics, I herein present a discussion on the incidence, diagnosis, and management of TKI-induced vascular adverse events.In 2013, there were cases in which clinical research papers on antihypertensive drugs conducted at five universities in Japan were retracted. Based on this case, the clinical research system in Japan was reviewed, and it was particularly required to strengthen the conflict of interest (COI) management system. Clinical Trial Act effected in April 2017 imposed a conflict of interest management obligation on researchers conducting clinical research. Conflict of interest management is accountability for the society and patients and protection of the cutting-edge research. This reviews the necessity and purpose of conflict of interest management and introduces the types of research and the required management of conflict of interest.
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