Aug 07, 2023

Transferrin uptake assay to measure Clathrin-mediated endocytosis in HIPCS derived neurons.

DOI
https://dx.doi.org/10.17504/protocols.io.n2bvj38d5lk5/v1
  • 1Waisman Center, University of Wisconsin-Madison, Madison, WI
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DOI: https://dx.doi.org/10.17504/protocols.io.n2bvj38d5lk5/v1
Protocol Citation: Sakthi Kumar 2023. Transferrin uptake assay to measure Clathrin-mediated endocytosis in HIPCS derived neurons.. protocols.io https://dx.doi.org/10.17504/protocols.io.n2bvj38d5lk5/v1
License: This is an open access  protocol  distributed under the terms of the  Creative Commons Attribution License,  which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: August 07, 2023
Last Modified: May 31, 2024
Protocol  Integer ID: 86063
Keywords: ASAPCRN, endocytosis, Clathrin, Transferrin uptake, transferrin uptake assay, transferrin uptake, endocytosis in hipc, mediated endocytosi, clathrin, derived neuron, other cell type, hipc
Funders Acknowledgements:
MJFF
Grant ID: 000301
Abstract
This protocol is used to measure Transferrin uptake as a way to investigate Clathrin-mediated endocytosis in HIPCS derived neurons, or other cell types.
Reagents needed:
1. Human Transferrin conjugated with Alexa Fluor 647 (Thermo Fisher, Catalog no: T23366).
Note: Transferrin conjugate is also available with Alexa Fluor 488, Alexa Fluor 546. The user may want to use a specific conjugate based on the need of their experiments. We have optimized this protocol for Transferrin conjugated with Alexa Fluor 647.
2. Basal Neuronal media- No added supplements like (N2, B27, NEAA, Glutamax and growth factors). 
Note: The user may use their desired neuronal medium, but they have to make sure that the media does not contain any Transferrin.
Preparation of Transferrin aliquots:
  1. Dissolve 5mg of Transferrin in 1 mL of Sterile PBS.
  2. Make the aliquots of desired volume and store at 2-8 C. 
  3. Protect them from light.
  4. Do not freeze the aliquots.
  5. For long term storage, add Sodium Azide.
Experimental Protocol
1h 26m
  1. Warm the basal neuronal media to 37 °C .
  2. Add warmed basal media to a new 24 well plate (500uls/ well needed) in the tissue culture hood.
  3. Transfer the coverslip with cells (neurons) into the well and proceed to starvation step.
  4. Starvation: starve the cells by keeping the plate in the humidified incubator (37 °C , 5% CO2) up to 01:00:00
  5. After 30 to 60 minutes, remove the plate from the incubator and add Transferrin (10ug/ml) to the cells and keep the plate in the incubator for 00:01:00 .
  6. After 1 minute, remove Transferrin and add 4% PFA for fixation.




1h 1m
PFA fixation:
  1. After adding 4% PFA wait for 00:15:00 for fixation.
  2. Then wash 3 times with PBS.
  3. Add Hoechst and incubate for 00:10:00 .
  4. Then wash 3 times with PBS and mount the coverslips on slides with Fluoromount G.
  5. Image the same day or keep the slides at 4 °C if imaging the next day.


25m
Quantification:
Use ImageJ based program to quantify Transferrin Fluorescence intensity. 
Notes:
Cell types tested:
We have tested Transferrin uptake in multiple cell types generated from H9 Embryonic Stem Cells.
  1. Cortical neurons.
  2. Midbrain Dopaminergic neurons.
  3. MGE derived GABA interneurons.
For the assay, we have used mature neurons from the above cell types (4 weeks after plating the progenitors).

Depending on the experiments, the user may want to test different concentrations of Transferrin and different time points of incubation. Also, the user may try pulse chase step to visualize recycling endosomes. For our experiments, we focused only on the initial uptake through Clathrin mediated endocytosis.