Jen-Wei Lin

Current Research

My main research focus is on the biophysical events underlying transmitter release and the membrane excitability of axons, using axons and synapses of the crayfish neuromuscular junction. There are three aspects to the research in my laboratory. First, we investigate the basic biophysical properties of ion channel distribution in motor axons. Second, as part of the class project for students in BI445, we use the crayfish preparation to study cellular mechanisms underlying the effects of pesticides and antiepileptic drugs (AED). Third, in collaboration with colleagues with physics and engineering expertise, we investigate the effects of ultrasound in the MHz range, and of pulsed infrared lasers, on neuronal excitability.

On the basic biophysical properties of the crayfish axon:

We take advantage of the accessibility of the crayfish axon, where simultaneous recordings from multiple locations are possible. We have demonstrated that voltage gated channels have a non-uniform density along the proximo-distal axis. Specifically, Na+ channel has a high density in the proximal, thick axonal branches and this density gradually decreases as axons branch and taper into terminal varicosities to the extent that terminals are unable to fire action potentials (Lin, 2013,16). On the other hand, there is a high density of a low threshold, fast K+ channel in the distal, thin branches and a low density in proximal axons (Lin, 2012). Why is there such non-uniformity in channel distribution? We propose that this distribution is optimized for preventing unintended “back-firing” of action potentials in distal branches.

On studies of industrial and clinical reagents:

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On collaboration with colleagues with physics and engineering expertise:

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In summary, my laboratory uses electrophysiological and imaging techniques to address basic neurophysiological questions related to axonal excitability. In addition, the crayfish preparation we use is proving versatile for mechanistic testing of drugs and industrial reagents at a cellular level, as well for interdisciplinary exploration of newly developed technologies on nervous system function.

Selected Publications

• X. Zhu, J.W. Lin, and M.Y. Sander (2019). Infrared inhibition and waveform modulation of action potentials in the crayfish motor axon. Biomedical Optics Express 10:6580-6594.
• S. Alshuaib, J. Mosaddeghi, and J.W. Lin (2020). Effects of levetiracetam on axon excitability and synaptic transmission at the crayfish neuromuscular junction. Synapse 74:e22154.
• X. Zhu, J.W. Lin, and M. Y. Sander (2020). Infrared inhibition impacts on locally initiated and propagating action potentials and the downstream synaptic transmission. Neurophotonics 7(4):045003.
• X. Zhu, J.W. Lin, A. Turnali, and M. Y. Sander (2021). Single infrared light pulses induce excitatory and inhibitory neuromodulation. Biomed Optics Express 13(1):374-388.
• N. Goldfeder, R. McDonald, S. Gaston, A. Harrison, D.H. Kim, C. MacIntosh, M. Moel Miranda, E. Odom, S. Nishad, W. Siwik, L. Zhang, and J.W. Lin (2022). Functions of potassium channels blocked by low micromolar 4-aminopyridine in the crayfish nervous system. Synapse. 76(7-8):e22234.
• F. Yu, W. S. Müller, G. Ehnholm, Y. Okada, and J.W. Lin (2022). Osmolarity effects on ultrasound-induced membrane depolarization in isolated crayfish motor axon. Ultrasound in Medicine & Biology 48(10):2040-2051.
• X. Zhu, J.W. Lin, and M. Y. Sander (2022). Bidirectional modulation of evoked synaptic transmission by pulsed infrared light. Scientific Reports 12(1):14196.
• F. Yu, W. S. Müller, G. Ehnholm, Y. Okada, and J.W. Lin (2023) Ultrasound-Induced Membrane Hyperpolarization in Motor Axons and Muscle Fibers of the Crayfish Neuromuscular Junction. Ultrasound Med Biol. 49(12):2527-2536.

Courses Taught:

• BI 349 Neurotoxins in biology, medicine, agriculture, and war
• BI 445/645 Cellular and molecular neurophysiology