The scale of urbanization in China during the past three decades is unprecedented in human history, and the processes are poorly understood. Here we present an effort to map the urban land expansion processes of 32 major cities in China from 1978 to 2010 using Landsat satellite data to understand the temporal and spatial characteristics. Results showed that the urban extent of the 32 cities expanded exponentially with very high annual rates varying from 3.2% to 12.8%. Temporal fluctuation in urban expansion rates in these 32 cities was obvious, with unexpected and alarming expansion rates from 2005 to 2010 that drastically exceeded their expectation, which was calculated from the long-term trend between 1978 and 2005, by 45%. Overall, we found that the growth rates of cities during the entire study period were inversely related to city size, contradicting the theory or Gibrat's law, which states that the growth rate is independent of city size. More detailed analysis indicated that city growth in China has transitioned from contradicting to conforming to Gibrat's law since 1995. Our study suggests that the urban expansion theory (i.e., Gibrat's law) does not fit Chinese expansion consistently over time, and the exact causes are unknown. Exploring the causes in future research will improve our understanding of the theory and, more importantly, understand the feasibility of the theoretical relationship between city size and expansion rate in guiding contemporary urban expansion planning.
Temporomandibular disorder (TMD) is a set of heterogeneous musculoskeletal conditions involving the temporomandibular joint (TMJ) and/or the masticatory muscles. Up to 33% of the population has had at least 1 symptom of TMD with 5% to 10% of them requiring treatment. Common symptoms include limited jaw movement, joint sound, and pain in the orofacial area. Once TMD becomes chronic, it can be debilitating with comorbidities that greatly reduce one's overall quality of life. However, the underlying mechanism of TMD is unclear because of the multicausative nature of the disease. Here, we report a novel mouse model of TMD where a bite block was placed in between the upper and lower incisors such that the mouth was kept maximally open for 1.5 hours per day for 5 days. After sustained mouth opening, mice developed persistent orofacial mechanical allodynia and TMJ dysfunction. At the cellular level, we found masseter muscle dystrophy, and increased proteoglycan deposition and hypertrophic chondrocytes in the mandibular condyle. Increased F4/80 macrophages were also observed in the masseter muscles and the TMJ posterior synovium. We also found ATF3 neuronal injury and increased F4/80 macrophages in the trigeminal ganglia. Microglia activation was observed in the trigeminal subnucleus caudalis. Inhibiting macrophage and microglia activation with a colony stimulating factor-1 receptor inhibitor prevented the development of orofacial mechanical allodynia, but not TMJ dysfunction. This study suggests that mouth opening for an extended period during dental treatments or oral intubations may risk the development of chronic TMD and inflammation associated with macrophage and microglia in the tissue and trigeminal system contributes to the development of TMD pain.
EGFRvIII contributes to the stemness of cancer stem cells through coexpression with CD133 in GBMs. Furthermore, CD133(+) /EGFRvIII(+) /EGFR(-) cells have the ability to initiate tumor formation and may contribute to gefitinib resistance.
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