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In the name of ALLAH ……….

In the name of ALLAH ………. Cell Injury-1. Adaptation of Cellular Growth and Differentiation. Dr. Shoaib Raza Associate Professor, Pathology, RIHS. Objective. The objectives of this lecture are: Introduce the term adaptation and cell injury

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In the name of ALLAH ……….

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  1. In the name of ALLAH ……….

  2. Cell Injury-1 Adaptation of Cellular Growth and Differentiation Dr. Shoaib Raza Associate Professor, Pathology, RIHS

  3. Objective • The objectives of this lecture are: • Introduce the term adaptation and cell injury • Define and brief explanation of various forms of adaptation; like • Hypertrophy • Hyperplasia • Atrophy • Metaplasia

  4. Cell injury • When the adaptive capabilities of the cell are exceeded, the cell injury ensues • Reversible cell injury • Irreversible cell injury • Cell death, necrosis or apoptosis • Causes of cell injury: • Ischemia • Chemical agent • Physical agent • Nutritional imbalance • Immunologic mechanism • Biological agent • Genetic derangements • Aging

  5. Adaptation • Adaptations are reversible change in the SIZE, NUMBER, PHENOTYPE, METABOLIC ACTIVITY or FUNCTIONS of the cells in response to changes in their environment. • Such adaptations may take several forms: • Hypertrophy • Hyperplasia • Atrophy • Metaplasia

  6. Hypertrophy • Increase in the size of cell resulting in an increase in the size of organ. • Seen in non-dividing cells • Pathologic hypertrophy • Physiologic hypertrophy • Causes may include: • Increased functional demand • Stimulation by hormone • Stimulation by growth factors • Increased work load

  7. Causes and examples of hypertrophy

  8. Mechanism of Hypertrophy • Result of increased production of cellular proteins • Increased actions of mechanical sensors triggered by increased work load • Growth factors (TGF-β, IGF-1, FGF, etc.) • Vasoactive agents (Endothelin-1, Angiotensin-II) • These stimuli work coordinately to increase the synthesis of muscle protein, responsible for hypertrophy

  9. Mechanism of Hypertrophy (continue) • Switch of contractile proteins from adult to fetal form • α-isoform of heavy chain of myosin is replaced by β-isoform • Reinduction of ANF • May be a combination of mechanical and chemical stimuli, leads to genetic and molecular rearrangements during hypertrophy

  10. Subcellular alterations • Sometimes a subcellular organelle may undergo hypertrophy • Endoplasmic reticulum of hepatocytes in barbiturates poisoning • Mitochondrial hypertrophy (giant mitochondria)

  11. Examples of hypertrophy Physiologic Hypertrophy Pathologic Hypertrophy • Myocardial hypertrophy • Prolonged hypertension • Breasts at puberty • Breasts during pregnancy • Uterus during pregnancy • Skeletal muscle hypertrophy in athletes

  12. Hyperplasia • An increase in the number of cells in an organ or tissue, usually resulting in increased mass of the organ or tissue. • Seen in the cells which are capable of dividing, and thus increasing the number of cells • Usually accompanied by hypertrophy as well • May be • Physiologic OR • Pathologic

  13. Physiologic Hyperplasia • Can be divided into: • Hormonal hyperplasia: • Proliferation of glandular epithelium of female breast at puberty and during pregnancy • Compensatory hyperplasia: • Live liver donors

  14. Pathologic Hyperplasia • Mostly caused by excessive hormone or growth factors acting on target cells • Endometrial hyperplasia • Benign prostatic hyperplasia • May be a characteristic response to certain viral infections. e.g. Human Papilloma Virus

  15. Mechanism of Hyperplasia • Is the result of growth factor-driven proliferation of mature cells • Or in some cases, increased output of new cells from tissue stem cells • After some minor hepatic injury, liver cells regenerate, under influence of certain growth factors • But if regenerative capacity of hepatocyte is compromised (e.g. in hepatitis), hepatocyte can instead regenerate from intrahepatic stem cells

  16. Normal endometrium (Proliferative phase) Endometrial Hyperplasia

  17. Examples of hyperplasia Physiologic Pathologic • Hyperplasia of breasts at puberty • Hyperplasia of breasts during pregnancy • Hyperplasia of endometrium during proliferative phase of menstrual cycle • Hyperplasia of bone marrow • Endometrial hyperplasia • Prostatic hyperplasia • Hyperplastic polyps in GIT • Hyperplasia of thyroid gland in Grave’s disease • Stratified squamous hyperplasia of skin and mucus membranes in HPV infection

  18. Consequences of hyperplasia • Increased cell number results in: • Increased functional capacity • Increase in the size of organ/tissue • Increased demand of nutrition and perfusion • In some cases hyperplasia presents a fertile soil for the development of cancer (neoplasia)

  19. Atrophy • Reduction in the size of cell associated with reduction in the size of tissue or organ • Can be • Physiologic: • During embryogenesis and metamorphosis • Uterus after parturition • Pathologic

  20. Causes of Atrophy • Pathologic atrophy: • Decreased work load (Disuse atrophy) • Loss of innervation (Denervation atrophy) • Diminished blood supply (Ischemic atrophy0 • Inadequate nutrition (Marasmus, cachexia) • Loss of endocrine stimulation • Pressure • Physiologic atrophy: • Senile atrophy • Hormonal atrophy in breasts or uterus

  21. Mechanism of atrophy • Decreased protein synthesis • Increased protein degradation • Increased autophagy (self eating) • Increased number of autophagic vacuoles (brown atrophy)

  22. metaplasia • One adult (differentiated) cell type is replaced by another cell type • Usually reversible • Almost always pathological • Columnar to squamous cell (chronic bronchitis) • Squamous to columnar (Barrett’s esophagus) • May be preneoplastic condition

  23. Any questions

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