Lysosomal Diseases
Lysosomal diseases, also known as lysosomal storage disorders (LSDs), is an inherited metabolic disorder that results from deficiencies in lysosomal enzymes or transport proteins. It leads to the accumulation of undigested substances within lysosomes. As a result, cellular waste products, lipids, and complex molecules cannot be properly broken down and recycled, causing progressive damage to tissues and organs. Lysosomal disease symptoms include neurological, skeletal, and visceral manifestations. Examples of Lysosomal diseases are Gaucher disease and Tay-Sachs disease.
Lysosomes – Definition, Types, Significance, Functions
Lysosomes are cell organelles that are also known as “suicide bags” or “cell recycling centers” of the cell. Lysosomes function in cellular waste disposal and programmed cell death (apoptosis). Lysosomes are eukaryotic membrane-bound cell organelles that appear small and spherical.
Lysosomes arise from the Golgi apparatus. They are the reservoirs of digestive enzymes. In this article, we will study in detail lysosome structure and function, diagram, and more.
Table of Content
- Lysosome Definition
- What are Lysosomes?
- Why Lysosomes are Known as Suicidal Bags?
- Lysosome Structure
- Lysosome Diagram
- Where are Lysosomal Enzymes made?
- Lysosome in Plant Cell
- Types of Lysosomes
- Significance of Lysosomes
- Functions of Lysosomes
- Lysosomal Diseases